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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs57221045

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr9:94621214-94621237 (GRCh38.p13) Help

The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.

Alleles
del(A)18 / del(A)17 / del(A)16 / d…

del(A)18 / del(A)17 / del(A)16 / del(A)15 / del(A)13 / del(A)12 / del(A)11 / del(A)10 / del(A)9 / del(A)8 / del(A)7 / del(A)6 / del(A)5 / del(A)4 / delAAA / delAA / delA / dupA

Variation Type
Indel Insertion and Deletion
Frequency
del(A)13=0.000 (0/360, ALFA)
del(A)12=0.000 (0/360, ALFA)
del(A)10=0.000 (0/360, ALFA) (+ 11 more)
del(A)9=0.000 (0/360, ALFA)
del(A)8=0.000 (0/360, ALFA)
del(A)7=0.000 (0/360, ALFA)
del(A)6=0.000 (0/360, ALFA)
del(A)5=0.000 (0/360, ALFA)
del(A)4=0.000 (0/360, ALFA)
delAAA=0.000 (0/360, ALFA)
delAA=0.000 (0/360, ALFA)
delA=0.000 (0/360, ALFA)
dupA=0.000 (0/360, ALFA)
delAA=0.20 (8/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
FBP1 : Intron Variant
Publications
0 citations
Genomic View
See rs on genome
Help

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements
Sequence name Change
GRCh38.p13 chr 9 NC_000009.12:g.94621220_94621237del
GRCh38.p13 chr 9 NC_000009.12:g.94621221_94621237del
GRCh38.p13 chr 9 NC_000009.12:g.94621222_94621237del
GRCh38.p13 chr 9 NC_000009.12:g.94621223_94621237del
GRCh38.p13 chr 9 NC_000009.12:g.94621225_94621237del
GRCh38.p13 chr 9 NC_000009.12:g.94621226_94621237del
GRCh38.p13 chr 9 NC_000009.12:g.94621227_94621237del
GRCh38.p13 chr 9 NC_000009.12:g.94621228_94621237del
GRCh38.p13 chr 9 NC_000009.12:g.94621229_94621237del
GRCh38.p13 chr 9 NC_000009.12:g.94621230_94621237del
GRCh38.p13 chr 9 NC_000009.12:g.94621231_94621237del
GRCh38.p13 chr 9 NC_000009.12:g.94621232_94621237del
GRCh38.p13 chr 9 NC_000009.12:g.94621233_94621237del
GRCh38.p13 chr 9 NC_000009.12:g.94621234_94621237del
GRCh38.p13 chr 9 NC_000009.12:g.94621235_94621237del
GRCh38.p13 chr 9 NC_000009.12:g.94621236_94621237del
GRCh38.p13 chr 9 NC_000009.12:g.94621237del
GRCh38.p13 chr 9 NC_000009.12:g.94621237dup
GRCh37.p13 chr 9 NC_000009.11:g.97383502_97383519del
GRCh37.p13 chr 9 NC_000009.11:g.97383503_97383519del
GRCh37.p13 chr 9 NC_000009.11:g.97383504_97383519del
GRCh37.p13 chr 9 NC_000009.11:g.97383505_97383519del
GRCh37.p13 chr 9 NC_000009.11:g.97383507_97383519del
GRCh37.p13 chr 9 NC_000009.11:g.97383508_97383519del
GRCh37.p13 chr 9 NC_000009.11:g.97383509_97383519del
GRCh37.p13 chr 9 NC_000009.11:g.97383510_97383519del
GRCh37.p13 chr 9 NC_000009.11:g.97383511_97383519del
GRCh37.p13 chr 9 NC_000009.11:g.97383512_97383519del
GRCh37.p13 chr 9 NC_000009.11:g.97383513_97383519del
GRCh37.p13 chr 9 NC_000009.11:g.97383514_97383519del
GRCh37.p13 chr 9 NC_000009.11:g.97383515_97383519del
GRCh37.p13 chr 9 NC_000009.11:g.97383516_97383519del
GRCh37.p13 chr 9 NC_000009.11:g.97383517_97383519del
GRCh37.p13 chr 9 NC_000009.11:g.97383518_97383519del
GRCh37.p13 chr 9 NC_000009.11:g.97383519del
GRCh37.p13 chr 9 NC_000009.11:g.97383519dup
FBP1 RefSeqGene NG_008174.1:g.24019_24036del
FBP1 RefSeqGene NG_008174.1:g.24020_24036del
FBP1 RefSeqGene NG_008174.1:g.24021_24036del
FBP1 RefSeqGene NG_008174.1:g.24022_24036del
FBP1 RefSeqGene NG_008174.1:g.24024_24036del
FBP1 RefSeqGene NG_008174.1:g.24025_24036del
FBP1 RefSeqGene NG_008174.1:g.24026_24036del
FBP1 RefSeqGene NG_008174.1:g.24027_24036del
FBP1 RefSeqGene NG_008174.1:g.24028_24036del
FBP1 RefSeqGene NG_008174.1:g.24029_24036del
FBP1 RefSeqGene NG_008174.1:g.24030_24036del
FBP1 RefSeqGene NG_008174.1:g.24031_24036del
FBP1 RefSeqGene NG_008174.1:g.24032_24036del
FBP1 RefSeqGene NG_008174.1:g.24033_24036del
FBP1 RefSeqGene NG_008174.1:g.24034_24036del
FBP1 RefSeqGene NG_008174.1:g.24035_24036del
FBP1 RefSeqGene NG_008174.1:g.24036del
FBP1 RefSeqGene NG_008174.1:g.24036dup
Gene: FBP1, fructose-bisphosphatase 1 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
FBP1 transcript variant 1 NM_000507.4:c.171-740_171…

NM_000507.4:c.171-740_171-723del

N/A Intron Variant
FBP1 transcript variant 2 NM_001127628.2:c.171-740_…

NM_001127628.2:c.171-740_171-723del

N/A Intron Variant
FBP1 transcript variant X1 XM_006717005.4:c.-76-740_…

XM_006717005.4:c.-76-740_-76-723del

N/A Intron Variant
Help

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20201027095038
Population Group Sample Size Ref Allele Alt Allele
Total Global 360 AAAAAAAAAAAAAAAAAAAAAAAA=1.000 AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000
European Sub 308 AAAAAAAAAAAAAAAAAAAAAAAA=1.000 AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000
African Sub 40 AAAAAAAAAAAAAAAAAAAAAAAA=1.00 AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00
African Others Sub 4 AAAAAAAAAAAAAAAAAAAAAAAA=1.0 AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0
African American Sub 36 AAAAAAAAAAAAAAAAAAAAAAAA=1.00 AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00
Asian Sub 2 AAAAAAAAAAAAAAAAAAAAAAAA=1.0 AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0
East Asian Sub 2 AAAAAAAAAAAAAAAAAAAAAAAA=1.0 AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0
Other Asian Sub 0 AAAAAAAAAAAAAAAAAAAAAAAA=0 AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0
Latin American 1 Sub 4 AAAAAAAAAAAAAAAAAAAAAAAA=1.0 AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0
Latin American 2 Sub 4 AAAAAAAAAAAAAAAAAAAAAAAA=1.0 AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0
South Asian Sub 0 AAAAAAAAAAAAAAAAAAAAAAAA=0 AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0
Other Sub 2 AAAAAAAAAAAAAAAAAAAAAAAA=1.0 AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0


Help

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download
Study Population Group Sample Size Ref Allele Alt Allele
The Danish reference pan genome Danish Study-wide 40 (A)24=0.80 delAA=0.20
Help

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement (A)24= del(A)18 del(A)17 del(A)16 del(A)15 del(A)13 del(A)12 del(A)11 del(A)10 del(A)9 del(A)8 del(A)7 del(A)6 del(A)5 del(A)4 delAAA delAA delA dupA
GRCh38.p13 chr 9 NC_000009.12:g.94621214_94621237= NC_000009.12:g.94621220_94621237del NC_000009.12:g.94621221_94621237del NC_000009.12:g.94621222_94621237del NC_000009.12:g.94621223_94621237del NC_000009.12:g.94621225_94621237del NC_000009.12:g.94621226_94621237del NC_000009.12:g.94621227_94621237del NC_000009.12:g.94621228_94621237del NC_000009.12:g.94621229_94621237del NC_000009.12:g.94621230_94621237del NC_000009.12:g.94621231_94621237del NC_000009.12:g.94621232_94621237del NC_000009.12:g.94621233_94621237del NC_000009.12:g.94621234_94621237del NC_000009.12:g.94621235_94621237del NC_000009.12:g.94621236_94621237del NC_000009.12:g.94621237del NC_000009.12:g.94621237dup
GRCh37.p13 chr 9 NC_000009.11:g.97383496_97383519= NC_000009.11:g.97383502_97383519del NC_000009.11:g.97383503_97383519del NC_000009.11:g.97383504_97383519del NC_000009.11:g.97383505_97383519del NC_000009.11:g.97383507_97383519del NC_000009.11:g.97383508_97383519del NC_000009.11:g.97383509_97383519del NC_000009.11:g.97383510_97383519del NC_000009.11:g.97383511_97383519del NC_000009.11:g.97383512_97383519del NC_000009.11:g.97383513_97383519del NC_000009.11:g.97383514_97383519del NC_000009.11:g.97383515_97383519del NC_000009.11:g.97383516_97383519del NC_000009.11:g.97383517_97383519del NC_000009.11:g.97383518_97383519del NC_000009.11:g.97383519del NC_000009.11:g.97383519dup
FBP1 RefSeqGene NG_008174.1:g.24013_24036= NG_008174.1:g.24019_24036del NG_008174.1:g.24020_24036del NG_008174.1:g.24021_24036del NG_008174.1:g.24022_24036del NG_008174.1:g.24024_24036del NG_008174.1:g.24025_24036del NG_008174.1:g.24026_24036del NG_008174.1:g.24027_24036del NG_008174.1:g.24028_24036del NG_008174.1:g.24029_24036del NG_008174.1:g.24030_24036del NG_008174.1:g.24031_24036del NG_008174.1:g.24032_24036del NG_008174.1:g.24033_24036del NG_008174.1:g.24034_24036del NG_008174.1:g.24035_24036del NG_008174.1:g.24036del NG_008174.1:g.24036dup
FBP1 transcript variant 1 NM_000507.3:c.171-723= NM_000507.3:c.171-740_171-723del NM_000507.3:c.171-739_171-723del NM_000507.3:c.171-738_171-723del NM_000507.3:c.171-737_171-723del NM_000507.3:c.171-735_171-723del NM_000507.3:c.171-734_171-723del NM_000507.3:c.171-733_171-723del NM_000507.3:c.171-732_171-723del NM_000507.3:c.171-731_171-723del NM_000507.3:c.171-730_171-723del NM_000507.3:c.171-729_171-723del NM_000507.3:c.171-728_171-723del NM_000507.3:c.171-727_171-723del NM_000507.3:c.171-726_171-723del NM_000507.3:c.171-725_171-723del NM_000507.3:c.171-724_171-723del NM_000507.3:c.171-723del NM_000507.3:c.171-746dup
FBP1 transcript variant 1 NM_000507.4:c.171-723= NM_000507.4:c.171-740_171-723del NM_000507.4:c.171-739_171-723del NM_000507.4:c.171-738_171-723del NM_000507.4:c.171-737_171-723del NM_000507.4:c.171-735_171-723del NM_000507.4:c.171-734_171-723del NM_000507.4:c.171-733_171-723del NM_000507.4:c.171-732_171-723del NM_000507.4:c.171-731_171-723del NM_000507.4:c.171-730_171-723del NM_000507.4:c.171-729_171-723del NM_000507.4:c.171-728_171-723del NM_000507.4:c.171-727_171-723del NM_000507.4:c.171-726_171-723del NM_000507.4:c.171-725_171-723del NM_000507.4:c.171-724_171-723del NM_000507.4:c.171-723del NM_000507.4:c.171-746dup
FBP1 transcript variant 2 NM_001127628.1:c.171-723= NM_001127628.1:c.171-740_171-723del NM_001127628.1:c.171-739_171-723del NM_001127628.1:c.171-738_171-723del NM_001127628.1:c.171-737_171-723del NM_001127628.1:c.171-735_171-723del NM_001127628.1:c.171-734_171-723del NM_001127628.1:c.171-733_171-723del NM_001127628.1:c.171-732_171-723del NM_001127628.1:c.171-731_171-723del NM_001127628.1:c.171-730_171-723del NM_001127628.1:c.171-729_171-723del NM_001127628.1:c.171-728_171-723del NM_001127628.1:c.171-727_171-723del NM_001127628.1:c.171-726_171-723del NM_001127628.1:c.171-725_171-723del NM_001127628.1:c.171-724_171-723del NM_001127628.1:c.171-723del NM_001127628.1:c.171-746dup
FBP1 transcript variant 2 NM_001127628.2:c.171-723= NM_001127628.2:c.171-740_171-723del NM_001127628.2:c.171-739_171-723del NM_001127628.2:c.171-738_171-723del NM_001127628.2:c.171-737_171-723del NM_001127628.2:c.171-735_171-723del NM_001127628.2:c.171-734_171-723del NM_001127628.2:c.171-733_171-723del NM_001127628.2:c.171-732_171-723del NM_001127628.2:c.171-731_171-723del NM_001127628.2:c.171-730_171-723del NM_001127628.2:c.171-729_171-723del NM_001127628.2:c.171-728_171-723del NM_001127628.2:c.171-727_171-723del NM_001127628.2:c.171-726_171-723del NM_001127628.2:c.171-725_171-723del NM_001127628.2:c.171-724_171-723del NM_001127628.2:c.171-723del NM_001127628.2:c.171-746dup
FBP1 transcript variant X1 XM_006717005.4:c.-76-723= XM_006717005.4:c.-76-740_-76-723del XM_006717005.4:c.-76-739_-76-723del XM_006717005.4:c.-76-738_-76-723del XM_006717005.4:c.-76-737_-76-723del XM_006717005.4:c.-76-735_-76-723del XM_006717005.4:c.-76-734_-76-723del XM_006717005.4:c.-76-733_-76-723del XM_006717005.4:c.-76-732_-76-723del XM_006717005.4:c.-76-731_-76-723del XM_006717005.4:c.-76-730_-76-723del XM_006717005.4:c.-76-729_-76-723del XM_006717005.4:c.-76-728_-76-723del XM_006717005.4:c.-76-727_-76-723del XM_006717005.4:c.-76-726_-76-723del XM_006717005.4:c.-76-725_-76-723del XM_006717005.4:c.-76-724_-76-723del XM_006717005.4:c.-76-723del XM_006717005.4:c.-76-746dup
Help

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

49 SubSNP, 23 Frequency submissions
No Submitter Submission ID Date (Build)
1 HGSV ss80101913 Dec 15, 2007 (129)
2 HGSV ss82197474 Dec 14, 2007 (129)
3 PJP ss295429364 May 09, 2011 (137)
4 PJP ss295429365 May 09, 2011 (134)
5 EVA_GENOME_DK ss1577424565 Apr 01, 2015 (144)
6 MCHAISSO ss3065236909 Nov 08, 2017 (151)
7 TOPMED ss3595281206 Jan 10, 2018 (151)
8 TOPMED ss3595281207 Nov 08, 2017 (151)
9 TOPMED ss3595281208 Nov 08, 2017 (151)
10 TOPMED ss3595281209 Nov 08, 2017 (151)
11 TOPMED ss3595281210 Nov 08, 2017 (151)
12 TOPMED ss3595281211 Nov 08, 2017 (151)
13 TOPMED ss3595281212 Nov 08, 2017 (151)
14 TOPMED ss3595281213 Nov 08, 2017 (151)
15 TOPMED ss3595281214 Nov 08, 2017 (151)
16 TOPMED ss3595281215 Nov 08, 2017 (151)
17 TOPMED ss3595281216 Nov 08, 2017 (151)
18 TOPMED ss3595281217 Nov 08, 2017 (151)
19 TOPMED ss3595281218 Nov 08, 2017 (151)
20 EVA_DECODE ss3724349822 Jul 13, 2019 (153)
21 EVA_DECODE ss3724349823 Jul 13, 2019 (153)
22 EVA_DECODE ss3724349824 Jul 13, 2019 (153)
23 EVA_DECODE ss3724349825 Jul 13, 2019 (153)
24 EVA_DECODE ss3724349826 Jul 13, 2019 (153)
25 PACBIO ss3791677976 Jul 13, 2019 (153)
26 PACBIO ss3791677977 Jul 13, 2019 (153)
27 PACBIO ss3796559401 Jul 13, 2019 (153)
28 PACBIO ss3796559402 Jul 13, 2019 (153)
29 GNOMAD ss4205906729 Apr 26, 2021 (155)
30 GNOMAD ss4205906730 Apr 26, 2021 (155)
31 GNOMAD ss4205906731 Apr 26, 2021 (155)
32 GNOMAD ss4205906732 Apr 26, 2021 (155)
33 GNOMAD ss4205906733 Apr 26, 2021 (155)
34 GNOMAD ss4205906734 Apr 26, 2021 (155)
35 GNOMAD ss4205906735 Apr 26, 2021 (155)
36 GNOMAD ss4205906736 Apr 26, 2021 (155)
37 GNOMAD ss4205906737 Apr 26, 2021 (155)
38 GNOMAD ss4205906738 Apr 26, 2021 (155)
39 GNOMAD ss4205906739 Apr 26, 2021 (155)
40 GNOMAD ss4205906740 Apr 26, 2021 (155)
41 GNOMAD ss4205906741 Apr 26, 2021 (155)
42 GNOMAD ss4205906742 Apr 26, 2021 (155)
43 GNOMAD ss4205906743 Apr 26, 2021 (155)
44 GNOMAD ss4205906744 Apr 26, 2021 (155)
45 TOMMO_GENOMICS ss5194372360 Apr 26, 2021 (155)
46 TOMMO_GENOMICS ss5194372361 Apr 26, 2021 (155)
47 TOMMO_GENOMICS ss5194372362 Apr 26, 2021 (155)
48 TOMMO_GENOMICS ss5194372363 Apr 26, 2021 (155)
49 TOMMO_GENOMICS ss5194372364 Apr 26, 2021 (155)
50 The Danish reference pan genome NC_000009.11 - 97383496 Apr 26, 2020 (154)
51 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 331749582 (NC_000009.12:94621213::A 9/39646)
Row 331749583 (NC_000009.12:94621213:AAA: 2079/39586)
Row 331749584 (NC_000009.12:94621213:AAAA: 263/39624)...

- Apr 26, 2021 (155)
52 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 331749582 (NC_000009.12:94621213::A 9/39646)
Row 331749583 (NC_000009.12:94621213:AAA: 2079/39586)
Row 331749584 (NC_000009.12:94621213:AAAA: 263/39624)...

- Apr 26, 2021 (155)
53 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 331749582 (NC_000009.12:94621213::A 9/39646)
Row 331749583 (NC_000009.12:94621213:AAA: 2079/39586)
Row 331749584 (NC_000009.12:94621213:AAAA: 263/39624)...

- Apr 26, 2021 (155)
54 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 331749582 (NC_000009.12:94621213::A 9/39646)
Row 331749583 (NC_000009.12:94621213:AAA: 2079/39586)
Row 331749584 (NC_000009.12:94621213:AAAA: 263/39624)...

- Apr 26, 2021 (155)
55 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 331749582 (NC_000009.12:94621213::A 9/39646)
Row 331749583 (NC_000009.12:94621213:AAA: 2079/39586)
Row 331749584 (NC_000009.12:94621213:AAAA: 263/39624)...

- Apr 26, 2021 (155)
56 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 331749582 (NC_000009.12:94621213::A 9/39646)
Row 331749583 (NC_000009.12:94621213:AAA: 2079/39586)
Row 331749584 (NC_000009.12:94621213:AAAA: 263/39624)...

- Apr 26, 2021 (155)
57 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 331749582 (NC_000009.12:94621213::A 9/39646)
Row 331749583 (NC_000009.12:94621213:AAA: 2079/39586)
Row 331749584 (NC_000009.12:94621213:AAAA: 263/39624)...

- Apr 26, 2021 (155)
58 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 331749582 (NC_000009.12:94621213::A 9/39646)
Row 331749583 (NC_000009.12:94621213:AAA: 2079/39586)
Row 331749584 (NC_000009.12:94621213:AAAA: 263/39624)...

- Apr 26, 2021 (155)
59 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 331749582 (NC_000009.12:94621213::A 9/39646)
Row 331749583 (NC_000009.12:94621213:AAA: 2079/39586)
Row 331749584 (NC_000009.12:94621213:AAAA: 263/39624)...

- Apr 26, 2021 (155)
60 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 331749582 (NC_000009.12:94621213::A 9/39646)
Row 331749583 (NC_000009.12:94621213:AAA: 2079/39586)
Row 331749584 (NC_000009.12:94621213:AAAA: 263/39624)...

- Apr 26, 2021 (155)
61 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 331749582 (NC_000009.12:94621213::A 9/39646)
Row 331749583 (NC_000009.12:94621213:AAA: 2079/39586)
Row 331749584 (NC_000009.12:94621213:AAAA: 263/39624)...

- Apr 26, 2021 (155)
62 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 331749582 (NC_000009.12:94621213::A 9/39646)
Row 331749583 (NC_000009.12:94621213:AAA: 2079/39586)
Row 331749584 (NC_000009.12:94621213:AAAA: 263/39624)...

- Apr 26, 2021 (155)
63 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 331749582 (NC_000009.12:94621213::A 9/39646)
Row 331749583 (NC_000009.12:94621213:AAA: 2079/39586)
Row 331749584 (NC_000009.12:94621213:AAAA: 263/39624)...

- Apr 26, 2021 (155)
64 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 331749582 (NC_000009.12:94621213::A 9/39646)
Row 331749583 (NC_000009.12:94621213:AAA: 2079/39586)
Row 331749584 (NC_000009.12:94621213:AAAA: 263/39624)...

- Apr 26, 2021 (155)
65 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 331749582 (NC_000009.12:94621213::A 9/39646)
Row 331749583 (NC_000009.12:94621213:AAA: 2079/39586)
Row 331749584 (NC_000009.12:94621213:AAAA: 263/39624)...

- Apr 26, 2021 (155)
66 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 331749582 (NC_000009.12:94621213::A 9/39646)
Row 331749583 (NC_000009.12:94621213:AAA: 2079/39586)
Row 331749584 (NC_000009.12:94621213:AAAA: 263/39624)...

- Apr 26, 2021 (155)
67 8.3KJPN

Submission ignored due to conflicting rows:
Row 52341667 (NC_000009.11:97383495:AA: 3551/15836)
Row 52341668 (NC_000009.11:97383495:A: 5044/15836)
Row 52341669 (NC_000009.11:97383495:AAAAA: 5/15836)...

- Apr 26, 2021 (155)
68 8.3KJPN

Submission ignored due to conflicting rows:
Row 52341667 (NC_000009.11:97383495:AA: 3551/15836)
Row 52341668 (NC_000009.11:97383495:A: 5044/15836)
Row 52341669 (NC_000009.11:97383495:AAAAA: 5/15836)...

- Apr 26, 2021 (155)
69 8.3KJPN

Submission ignored due to conflicting rows:
Row 52341667 (NC_000009.11:97383495:AA: 3551/15836)
Row 52341668 (NC_000009.11:97383495:A: 5044/15836)
Row 52341669 (NC_000009.11:97383495:AAAAA: 5/15836)...

- Apr 26, 2021 (155)
70 8.3KJPN

Submission ignored due to conflicting rows:
Row 52341667 (NC_000009.11:97383495:AA: 3551/15836)
Row 52341668 (NC_000009.11:97383495:A: 5044/15836)
Row 52341669 (NC_000009.11:97383495:AAAAA: 5/15836)...

- Apr 26, 2021 (155)
71 8.3KJPN

Submission ignored due to conflicting rows:
Row 52341667 (NC_000009.11:97383495:AA: 3551/15836)
Row 52341668 (NC_000009.11:97383495:A: 5044/15836)
Row 52341669 (NC_000009.11:97383495:AAAAA: 5/15836)...

- Apr 26, 2021 (155)
72 ALFA NC_000009.12 - 94621214 Apr 26, 2021 (155)
Help

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID History Updated (Build)
rs140049982 May 11, 2012 (137)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss4205906744 NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAA:

NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAA

ss4205906743 NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAA:

NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAA

ss4205906742 NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAA:

NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA

ss4205906741 NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAA:

NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA

ss3595281218, ss4205906740 NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAA:

NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA

(self)
10012689272 NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA

NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA

ss3595281217, ss4205906739 NC_000009.12:94621213:AAAAAAAAAAAA: NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA

(self)
10012689272 NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA

NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA

ss4205906738 NC_000009.12:94621213:AAAAAAAAAAA: NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA

ss3595281216, ss3724349826, ss4205906737 NC_000009.12:94621213:AAAAAAAAAA: NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA

(self)
10012689272 NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA

NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA

ss5194372364 NC_000009.11:97383495:AAAAAAAAA: NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA

ss3595281215, ss4205906736 NC_000009.12:94621213:AAAAAAAAA: NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA

(self)
10012689272 NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA

NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA

ss3595281214, ss4205906735 NC_000009.12:94621213:AAAAAAAA: NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA

(self)
10012689272 NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA

NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA

ss3595281213, ss4205906734 NC_000009.12:94621213:AAAAAAA: NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA

(self)
10012689272 NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA

NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA

ss3595281212, ss4205906733 NC_000009.12:94621213:AAAAAA: NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA

(self)
10012689272 NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA

NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA

ss5194372362 NC_000009.11:97383495:AAAAA: NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA

ss3595281211, ss4205906732 NC_000009.12:94621213:AAAAA: NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA

(self)
10012689272 NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA

NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA

ss3595281210, ss4205906731 NC_000009.12:94621213:AAAA: NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA

(self)
10012689272 NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA

NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA

ss3724349825 NC_000009.12:94621219:AAAA: NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA

(self)
ss5194372363 NC_000009.11:97383495:AAA: NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA

ss3595281209, ss4205906730 NC_000009.12:94621213:AAA: NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA

(self)
10012689272 NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA

NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA

ss3724349824 NC_000009.12:94621220:AAA: NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA

(self)
ss80101913 NC_000009.9:94463072:AA: NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA

(self)
1289627, ss1577424565, ss3791677976, ss3796559401, ss5194372360 NC_000009.11:97383495:AA: NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA

(self)
ss3065236909, ss3595281208 NC_000009.12:94621213:AA: NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA

(self)
10012689272 NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA

NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA

ss3724349823 NC_000009.12:94621221:AA: NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA

(self)
ss82197474 NC_000009.9:94463073:A: NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA

(self)
ss295429364 NC_000009.10:96423316:A: NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA

(self)
ss295429365 NC_000009.10:96423339:A: NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA

(self)
ss3791677977, ss3796559402, ss5194372361 NC_000009.11:97383495:A: NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA

(self)
ss3595281207 NC_000009.12:94621213:A: NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA

(self)
10012689272 NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA

NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA

ss3724349822 NC_000009.12:94621222:A: NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA

(self)
ss3595281206, ss4205906729 NC_000009.12:94621213::A NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA

(self)
10012689272 NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA

NC_000009.12:94621213:AAAAAAAAAAAA…

NC_000009.12:94621213:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA

Help

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs57221045

Help

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:
Select flank length:

Genomic regions, transcripts, and products
Top Help

NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Software version is: 2.0.1.post596+ae089ad