Name: rs56730196
Published: September 21, 2022
License: Open Access

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.

rs56730196

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:224139753-224139767 (GRCh38.p14) 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(GCAT)₃ / del(GCAT)₂ / delGCAT …
del(GCAT)₃ / del(GCAT)₂ / delGCAT / dupGCAT / dup(GCAT)₂ / dup(GCAT)₃ / ins(GCAT)₄ / ins(GCAT)₅
Variation Type: Indel Insertion and Deletion
Frequency: dupGCAT=0.01580 (238/15065, ALFA)
dup(GCAT)₃=0.0016 (3/1820, Korea1K)
dupGCAT=0.015 (9/586, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: FBXO28 : Intron Variant
LOC124903813 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

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: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	15065	CATGCATGCATGCAT=0.98387	CAT=0.00000, CATGCAT=0.00000, CATGCATGCAT=0.00000, CATGCATGCATGCATGCAT=0.01580, CATGCATGCATGCATGCATGCATGCAT=0.00033, CATGCATGCATGCATGCATGCAT=0.00000, CATGCATGCATGCATGCATGCATGCATGCAT=0.00000, CATGCATGCATGCATGCATGCATGCATGCATGCAT=0.00000
European	Sub	11349	CATGCATGCATGCAT=0.97868	CAT=0.00000, CATGCAT=0.00000, CATGCATGCAT=0.00000, CATGCATGCATGCATGCAT=0.02088, CATGCATGCATGCATGCATGCATGCAT=0.00044, CATGCATGCATGCATGCATGCAT=0.00000, CATGCATGCATGCATGCATGCATGCATGCAT=0.00000, CATGCATGCATGCATGCATGCATGCATGCATGCAT=0.00000
African	Sub	2344	CATGCATGCATGCAT=1.0000	CAT=0.0000, CATGCAT=0.0000, CATGCATGCAT=0.0000, CATGCATGCATGCATGCAT=0.0000, CATGCATGCATGCATGCATGCATGCAT=0.0000, CATGCATGCATGCATGCATGCAT=0.0000, CATGCATGCATGCATGCATGCATGCATGCAT=0.0000, CATGCATGCATGCATGCATGCATGCATGCATGCAT=0.0000
African Others	Sub	88	CATGCATGCATGCAT=1.00	CAT=0.00, CATGCAT=0.00, CATGCATGCAT=0.00, CATGCATGCATGCATGCAT=0.00, CATGCATGCATGCATGCATGCATGCAT=0.00, CATGCATGCATGCATGCATGCAT=0.00, CATGCATGCATGCATGCATGCATGCATGCAT=0.00, CATGCATGCATGCATGCATGCATGCATGCATGCAT=0.00
African American	Sub	2256	CATGCATGCATGCAT=1.0000	CAT=0.0000, CATGCAT=0.0000, CATGCATGCAT=0.0000, CATGCATGCATGCATGCAT=0.0000, CATGCATGCATGCATGCATGCATGCAT=0.0000, CATGCATGCATGCATGCATGCAT=0.0000, CATGCATGCATGCATGCATGCATGCATGCAT=0.0000, CATGCATGCATGCATGCATGCATGCATGCATGCAT=0.0000
Asian	Sub	106	CATGCATGCATGCAT=1.000	CAT=0.000, CATGCAT=0.000, CATGCATGCAT=0.000, CATGCATGCATGCATGCAT=0.000, CATGCATGCATGCATGCATGCATGCAT=0.000, CATGCATGCATGCATGCATGCAT=0.000, CATGCATGCATGCATGCATGCATGCATGCAT=0.000, CATGCATGCATGCATGCATGCATGCATGCATGCAT=0.000
East Asian	Sub	82	CATGCATGCATGCAT=1.00	CAT=0.00, CATGCAT=0.00, CATGCATGCAT=0.00, CATGCATGCATGCATGCAT=0.00, CATGCATGCATGCATGCATGCATGCAT=0.00, CATGCATGCATGCATGCATGCAT=0.00, CATGCATGCATGCATGCATGCATGCATGCAT=0.00, CATGCATGCATGCATGCATGCATGCATGCATGCAT=0.00
Other Asian	Sub	24	CATGCATGCATGCAT=1.00	CAT=0.00, CATGCAT=0.00, CATGCATGCAT=0.00, CATGCATGCATGCATGCAT=0.00, CATGCATGCATGCATGCATGCATGCAT=0.00, CATGCATGCATGCATGCATGCAT=0.00, CATGCATGCATGCATGCATGCATGCATGCAT=0.00, CATGCATGCATGCATGCATGCATGCATGCATGCAT=0.00
Latin American 1	Sub	138	CATGCATGCATGCAT=1.000	CAT=0.000, CATGCAT=0.000, CATGCATGCAT=0.000, CATGCATGCATGCATGCAT=0.000, CATGCATGCATGCATGCATGCATGCAT=0.000, CATGCATGCATGCATGCATGCAT=0.000, CATGCATGCATGCATGCATGCATGCATGCAT=0.000, CATGCATGCATGCATGCATGCATGCATGCATGCAT=0.000
Latin American 2	Sub	594	CATGCATGCATGCAT=1.000	CAT=0.000, CATGCAT=0.000, CATGCATGCAT=0.000, CATGCATGCATGCATGCAT=0.000, CATGCATGCATGCATGCATGCATGCAT=0.000, CATGCATGCATGCATGCATGCAT=0.000, CATGCATGCATGCATGCATGCATGCATGCAT=0.000, CATGCATGCATGCATGCATGCATGCATGCATGCAT=0.000
South Asian	Sub	90	CATGCATGCATGCAT=1.00	CAT=0.00, CATGCAT=0.00, CATGCATGCAT=0.00, CATGCATGCATGCATGCAT=0.00, CATGCATGCATGCATGCATGCATGCAT=0.00, CATGCATGCATGCATGCATGCAT=0.00, CATGCATGCATGCATGCATGCATGCATGCAT=0.00, CATGCATGCATGCATGCATGCATGCATGCATGCAT=0.00
Other	Sub	444	CATGCATGCATGCAT=0.998	CAT=0.000, CATGCAT=0.000, CATGCATGCAT=0.000, CATGCATGCATGCATGCAT=0.002, CATGCATGCATGCATGCATGCATGCAT=0.000, CATGCATGCATGCATGCATGCAT=0.000, CATGCATGCATGCATGCATGCATGCATGCAT=0.000, CATGCATGCATGCATGCATGCATGCATGCATGCAT=0.000

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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	15065	(CATG)₃CAT=0.98387	del(GCAT)₃=0.00000, del(GCAT)₂=0.00000, delGCAT=0.00000, dupGCAT=0.01580, dup(GCAT)₂=0.00000, dup(GCAT)₃=0.00033, ins(GCAT)₄=0.00000, ins(GCAT)₅=0.00000
Allele Frequency Aggregator	European	Sub	11349	(CATG)₃CAT=0.97868	del(GCAT)₃=0.00000, del(GCAT)₂=0.00000, delGCAT=0.00000, dupGCAT=0.02088, dup(GCAT)₂=0.00000, dup(GCAT)₃=0.00044, ins(GCAT)₄=0.00000, ins(GCAT)₅=0.00000
Allele Frequency Aggregator	African	Sub	2344	(CATG)₃CAT=1.0000	del(GCAT)₃=0.0000, del(GCAT)₂=0.0000, delGCAT=0.0000, dupGCAT=0.0000, dup(GCAT)₂=0.0000, dup(GCAT)₃=0.0000, ins(GCAT)₄=0.0000, ins(GCAT)₅=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	594	(CATG)₃CAT=1.000	del(GCAT)₃=0.000, del(GCAT)₂=0.000, delGCAT=0.000, dupGCAT=0.000, dup(GCAT)₂=0.000, dup(GCAT)₃=0.000, ins(GCAT)₄=0.000, ins(GCAT)₅=0.000
Allele Frequency Aggregator	Other	Sub	444	(CATG)₃CAT=0.998	del(GCAT)₃=0.000, del(GCAT)₂=0.000, delGCAT=0.000, dupGCAT=0.002, dup(GCAT)₂=0.000, dup(GCAT)₃=0.000, ins(GCAT)₄=0.000, ins(GCAT)₅=0.000
Allele Frequency Aggregator	Latin American 1	Sub	138	(CATG)₃CAT=1.000	del(GCAT)₃=0.000, del(GCAT)₂=0.000, delGCAT=0.000, dupGCAT=0.000, dup(GCAT)₂=0.000, dup(GCAT)₃=0.000, ins(GCAT)₄=0.000, ins(GCAT)₅=0.000
Allele Frequency Aggregator	Asian	Sub	106	(CATG)₃CAT=1.000	del(GCAT)₃=0.000, del(GCAT)₂=0.000, delGCAT=0.000, dupGCAT=0.000, dup(GCAT)₂=0.000, dup(GCAT)₃=0.000, ins(GCAT)₄=0.000, ins(GCAT)₅=0.000
Allele Frequency Aggregator	South Asian	Sub	90	(CATG)₃CAT=1.00	del(GCAT)₃=0.00, del(GCAT)₂=0.00, delGCAT=0.00, dupGCAT=0.00, dup(GCAT)₂=0.00, dup(GCAT)₃=0.00, ins(GCAT)₄=0.00, ins(GCAT)₅=0.00
Korean Genome Project	KOREAN	Study-wide	1820	- No frequency provided	dup(GCAT)₃=0.0016
Northern Sweden	ACPOP	Study-wide	586	- No frequency provided	dupGCAT=0.015

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.p14 chr 1	NC_000001.11:g.224139756_224139767del
GRCh38.p14 chr 1	NC_000001.11:g.224139756GCAT[1]
GRCh38.p14 chr 1	NC_000001.11:g.224139756GCAT[2]
GRCh38.p14 chr 1	NC_000001.11:g.224139756GCAT[4]
GRCh38.p14 chr 1	NC_000001.11:g.224139756GCAT[5]
GRCh38.p14 chr 1	NC_000001.11:g.224139756GCAT[6]
GRCh38.p14 chr 1	NC_000001.11:g.224139756GCAT[7]
GRCh38.p14 chr 1	NC_000001.11:g.224139756GCAT[8]
GRCh37.p13 chr 1	NC_000001.10:g.224327458_224327469del
GRCh37.p13 chr 1	NC_000001.10:g.224327458GCAT[1]
GRCh37.p13 chr 1	NC_000001.10:g.224327458GCAT[2]
GRCh37.p13 chr 1	NC_000001.10:g.224327458GCAT[4]
GRCh37.p13 chr 1	NC_000001.10:g.224327458GCAT[5]
GRCh37.p13 chr 1	NC_000001.10:g.224327458GCAT[6]
GRCh37.p13 chr 1	NC_000001.10:g.224327458GCAT[7]
GRCh37.p13 chr 1	NC_000001.10:g.224327458GCAT[8]

Gene: FBXO28, F-box protein 28 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
FBXO28 transcript variant 2	NM_001136115.3:c.516+5544… NM_001136115.3:c.516+5544_516+5555del	N/A	Intron Variant
FBXO28 transcript variant 1	NM_015176.4:c.516+5544_51… NM_015176.4:c.516+5544_516+5555del	N/A	Intron Variant
FBXO28 transcript variant 3	NR_049764.2:n.	N/A	Intron Variant

Gene: LOC124903813, uncharacterized LOC124903813 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC124903813 transcript	XM_047436340.1:c.246+2817… XM_047436340.1:c.246+2817_246+2828del	N/A	Intron Variant

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

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	(CATG)₃CAT=	del(GCAT)₃	del(GCAT)₂	delGCAT	dupGCAT	dup(GCAT)₂	dup(GCAT)₃	ins(GCAT)₄	ins(GCAT)₅
GRCh38.p14 chr 1	NC_000001.11:g.224139753_224139767=	NC_000001.11:g.224139756_224139767del	NC_000001.11:g.224139756GCAT[1]	NC_000001.11:g.224139756GCAT[2]	NC_000001.11:g.224139756GCAT[4]	NC_000001.11:g.224139756GCAT[5]	NC_000001.11:g.224139756GCAT[6]	NC_000001.11:g.224139756GCAT[7]	NC_000001.11:g.224139756GCAT[8]
GRCh37.p13 chr 1	NC_000001.10:g.224327455_224327469=	NC_000001.10:g.224327458_224327469del	NC_000001.10:g.224327458GCAT[1]	NC_000001.10:g.224327458GCAT[2]	NC_000001.10:g.224327458GCAT[4]	NC_000001.10:g.224327458GCAT[5]	NC_000001.10:g.224327458GCAT[6]	NC_000001.10:g.224327458GCAT[7]	NC_000001.10:g.224327458GCAT[8]
FBXO28 transcript variant 2	NM_001136115.2:c.516+5541=	NM_001136115.2:c.516+5544_516+5555del	NM_001136115.2:c.516+5548_516+5555del	NM_001136115.2:c.516+5541CATG[2]	NM_001136115.2:c.516+5541CATG[4]	NM_001136115.2:c.516+5541CATG[5]	NM_001136115.2:c.516+5541CATG[6]	NM_001136115.2:c.516+5541CATG[7]	NM_001136115.2:c.516+5541CATG[8]
FBXO28 transcript variant 2	NM_001136115.3:c.516+5541=	NM_001136115.3:c.516+5544_516+5555del	NM_001136115.3:c.516+5548_516+5555del	NM_001136115.3:c.516+5541CATG[2]	NM_001136115.3:c.516+5541CATG[4]	NM_001136115.3:c.516+5541CATG[5]	NM_001136115.3:c.516+5541CATG[6]	NM_001136115.3:c.516+5541CATG[7]	NM_001136115.3:c.516+5541CATG[8]
FBXO28 transcript variant 1	NM_015176.3:c.516+5541=	NM_015176.3:c.516+5544_516+5555del	NM_015176.3:c.516+5548_516+5555del	NM_015176.3:c.516+5541CATG[2]	NM_015176.3:c.516+5541CATG[4]	NM_015176.3:c.516+5541CATG[5]	NM_015176.3:c.516+5541CATG[6]	NM_015176.3:c.516+5541CATG[7]	NM_015176.3:c.516+5541CATG[8]
FBXO28 transcript variant 1	NM_015176.4:c.516+5541=	NM_015176.4:c.516+5544_516+5555del	NM_015176.4:c.516+5548_516+5555del	NM_015176.4:c.516+5541CATG[2]	NM_015176.4:c.516+5541CATG[4]	NM_015176.4:c.516+5541CATG[5]	NM_015176.4:c.516+5541CATG[6]	NM_015176.4:c.516+5541CATG[7]	NM_015176.4:c.516+5541CATG[8]
LOC124903813 transcript	XM_047436340.1:c.246+2828=	XM_047436340.1:c.246+2817_246+2828del	XM_047436340.1:c.246+2821_246+2828del	XM_047436340.1:c.246+2817CATG[2]	XM_047436340.1:c.246+2817CATG[4]	XM_047436340.1:c.246+2817CATG[5]	XM_047436340.1:c.246+2817CATG[6]	XM_047436340.1:c.246+2817CATG[7]	XM_047436340.1:c.246+2817CATG[8]

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#.

30 SubSNP, 16 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	EVA_DECODE	ss3688728229	Jul 12, 2019 (153)
2	EVA_DECODE	ss3688728230	Jul 12, 2019 (153)
3	EVA_DECODE	ss3688728231	Jul 12, 2019 (153)
4	EVA_DECODE	ss3688728232	Jul 12, 2019 (153)
5	ACPOP	ss3727907171	Jul 12, 2019 (153)
6	EVA	ss3826670240	Apr 25, 2020 (154)
7	KOGIC	ss3946593260	Apr 25, 2020 (154)
8	GNOMAD	ss4012174875	Apr 25, 2021 (155)
9	GNOMAD	ss4012174876	Apr 25, 2021 (155)
10	GNOMAD	ss4012174877	Apr 25, 2021 (155)
11	GNOMAD	ss4012174878	Apr 25, 2021 (155)
12	GNOMAD	ss4012174883	Apr 25, 2021 (155)
13	TOMMO_GENOMICS	ss5148661349	Apr 25, 2021 (155)
14	TOMMO_GENOMICS	ss5148661350	Apr 25, 2021 (155)
15	TOMMO_GENOMICS	ss5148661351	Apr 25, 2021 (155)
16	TOMMO_GENOMICS	ss5148661352	Apr 25, 2021 (155)
17	1000G_HIGH_COVERAGE	ss5245972301	Oct 12, 2022 (156)
18	1000G_HIGH_COVERAGE	ss5245972302	Oct 12, 2022 (156)
19	1000G_HIGH_COVERAGE	ss5245972305	Oct 12, 2022 (156)
20	1000G_HIGH_COVERAGE	ss5245972306	Oct 12, 2022 (156)
21	HUGCELL_USP	ss5446390043	Oct 12, 2022 (156)
22	HUGCELL_USP	ss5446390044	Oct 12, 2022 (156)
23	TOMMO_GENOMICS	ss5676485955	Oct 12, 2022 (156)
24	TOMMO_GENOMICS	ss5676485956	Oct 12, 2022 (156)
25	TOMMO_GENOMICS	ss5676485958	Oct 12, 2022 (156)
26	TOMMO_GENOMICS	ss5676485959	Oct 12, 2022 (156)
27	YY_MCH	ss5801683639	Oct 12, 2022 (156)
28	EVA	ss5833333447	Oct 12, 2022 (156)
29	EVA	ss5833333448	Oct 12, 2022 (156)
30	EVA	ss5833333449	Oct 12, 2022 (156)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 41036676 (NC_000001.11:224139752::CATG 6580/101526) Row 41036677 (NC_000001.11:224139752::CATGCATG 86/101592) Row 41036678 (NC_000001.11:224139752::CATGCATGCATG 18/101600)...	-	Apr 25, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 41036676 (NC_000001.11:224139752::CATG 6580/101526) Row 41036677 (NC_000001.11:224139752::CATGCATG 86/101592) Row 41036678 (NC_000001.11:224139752::CATGCATGCATG 18/101600)...	-	Apr 25, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 41036676 (NC_000001.11:224139752::CATG 6580/101526) Row 41036677 (NC_000001.11:224139752::CATGCATG 86/101592) Row 41036678 (NC_000001.11:224139752::CATGCATGCATG 18/101600)...	-	Apr 25, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 41036676 (NC_000001.11:224139752::CATG 6580/101526) Row 41036677 (NC_000001.11:224139752::CATGCATG 86/101592) Row 41036678 (NC_000001.11:224139752::CATGCATGCATG 18/101600)...	-	Apr 25, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 41036676 (NC_000001.11:224139752::CATG 6580/101526) Row 41036677 (NC_000001.11:224139752::CATGCATG 86/101592) Row 41036678 (NC_000001.11:224139752::CATGCATGCATG 18/101600)...	-	Apr 25, 2021 (155)
36	Korean Genome Project	NC_000001.11 - 224139757	Apr 25, 2020 (154)
37	Northern Sweden	NC_000001.10 - 224327455	Jul 12, 2019 (153)
38	8.3KJPN Submission ignored due to conflicting rows: Row 6630656 (NC_000001.10:224327454::CATG 1/16588) Row 6630657 (NC_000001.10:224327454::CATGCATGCATG 9/16588) Row 6630658 (NC_000001.10:224327454:CATGCATGCATG: 10/16588)...	-	Apr 25, 2021 (155)
39	8.3KJPN Submission ignored due to conflicting rows: Row 6630656 (NC_000001.10:224327454::CATG 1/16588) Row 6630657 (NC_000001.10:224327454::CATGCATGCATG 9/16588) Row 6630658 (NC_000001.10:224327454:CATGCATGCATG: 10/16588)...	-	Apr 25, 2021 (155)
40	8.3KJPN Submission ignored due to conflicting rows: Row 6630656 (NC_000001.10:224327454::CATG 1/16588) Row 6630657 (NC_000001.10:224327454::CATGCATGCATG 9/16588) Row 6630658 (NC_000001.10:224327454:CATGCATGCATG: 10/16588)...	-	Apr 25, 2021 (155)
41	8.3KJPN Submission ignored due to conflicting rows: Row 6630656 (NC_000001.10:224327454::CATG 1/16588) Row 6630657 (NC_000001.10:224327454::CATGCATGCATG 9/16588) Row 6630658 (NC_000001.10:224327454:CATGCATGCATG: 10/16588)...	-	Apr 25, 2021 (155)
42	14KJPN Submission ignored due to conflicting rows: Row 10323059 (NC_000001.11:224139752::CATG 4/28256) Row 10323060 (NC_000001.11:224139752::CATGCATGCATG 19/28256) Row 10323062 (NC_000001.11:224139752:CATGCATGCATG: 14/28256)...	-	Oct 12, 2022 (156)
43	14KJPN Submission ignored due to conflicting rows: Row 10323059 (NC_000001.11:224139752::CATG 4/28256) Row 10323060 (NC_000001.11:224139752::CATGCATGCATG 19/28256) Row 10323062 (NC_000001.11:224139752:CATGCATGCATG: 14/28256)...	-	Oct 12, 2022 (156)
44	14KJPN Submission ignored due to conflicting rows: Row 10323059 (NC_000001.11:224139752::CATG 4/28256) Row 10323060 (NC_000001.11:224139752::CATGCATGCATG 19/28256) Row 10323062 (NC_000001.11:224139752:CATGCATGCATG: 14/28256)...	-	Oct 12, 2022 (156)
45	14KJPN Submission ignored due to conflicting rows: Row 10323059 (NC_000001.11:224139752::CATG 4/28256) Row 10323060 (NC_000001.11:224139752::CATGCATGCATG 19/28256) Row 10323062 (NC_000001.11:224139752:CATGCATGCATG: 14/28256)...	-	Oct 12, 2022 (156)
46	ALFA	NC_000001.11 - 224139753	Apr 25, 2021 (155)

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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5148661351	NC_000001.10:224327454:CATGCATGCAT… NC_000001.10:224327454:CATGCATGCATG:	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CAT	(self)
ss4012174883, ss5245972306, ss5676485958	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATG:	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CAT	(self)
2523515374	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CAT	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CAT	(self)
2523515374	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CATGCAT	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CATGCAT	(self)
ss3688728232	NC_000001.11:224139752:CATG:	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CATGCATGCAT	(self)
2523515374	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CATGCATGCAT	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CATGCATGCAT	(self)
1192036, ss3727907171, ss3826670240, ss5148661349, ss5833333447	NC_000001.10:224327454::CATG	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CATGCATGCATGCATGCAT	(self)
ss4012174875, ss5245972301, ss5446390043, ss5676485955, ss5801683639	NC_000001.11:224139752::CATG	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CATGCATGCATGCATGCAT	(self)
2523515374	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CATGCATGCATGCATGCAT	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CATGCATGCATGCATGCAT	(self)
ss3688728231	NC_000001.11:224139756::CATG	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CATGCATGCATGCATGCAT	(self)
ss5833333449	NC_000001.10:224327454::CATGCATG	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CATGCATGCATGCATGCATGCAT
ss4012174876, ss5245972302, ss5446390044	NC_000001.11:224139752::CATGCATG	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CATGCATGCATGCATGCATGCAT	(self)
2523515374	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CATGCATGCATGCATGCATGCAT	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CATGCATGCATGCATGCATGCAT	(self)
ss3688728230	NC_000001.11:224139756::CATGCATG	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CATGCATGCATGCATGCATGCAT	(self)
ss5148661350, ss5833333448	NC_000001.10:224327454::CATGCATGCA… NC_000001.10:224327454::CATGCATGCATG	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CATGCATGCATGCATGCATGCATGCAT	(self)
ss4012174877, ss5676485956	NC_000001.11:224139752::CATGCATGCA… NC_000001.11:224139752::CATGCATGCATG	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CATGCATGCATGCATGCATGCATGCAT	(self)
2523515374	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CATGCATGCATGCATGCATGCATGCAT	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CATGCATGCATGCATGCATGCATGCAT	(self)
2971261, ss3688728229, ss3946593260	NC_000001.11:224139756::CATGCATGCA… NC_000001.11:224139756::CATGCATGCATG	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CATGCATGCATGCATGCATGCATGCAT	(self)
ss4012174878, ss5245972305	NC_000001.11:224139752::CATGCATGCA… NC_000001.11:224139752::CATGCATGCATGCATG	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CATGCATGCATGCATGCATGCATGCATGCAT	(self)
2523515374	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CATGCATGCATGCATGCATGCATGCATGCAT	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CATGCATGCATGCATGCATGCATGCATGCAT	(self)
ss5148661352	NC_000001.10:224327454::CATGCATGCA… NC_000001.10:224327454::CATGCATGCATGCATGCATG	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CATGCATGCATGCATGCATGCATGCATGCATGCAT	(self)
ss5676485959	NC_000001.11:224139752::CATGCATGCA… NC_000001.11:224139752::CATGCATGCATGCATGCATG	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CATGCATGCATGCATGCATGCATGCATGCATGCAT	(self)
2523515374	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CATGCATGCATGCATGCATGCATGCATGCATGCAT	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CATGCATGCATGCATGCATGCATGCATGCATGCAT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3104710774	NC_000001.11:224139752:CATGCATG:	NC_000001.11:224139752:CATGCATGCAT… NC_000001.11:224139752:CATGCATGCATGCAT:CATGCAT

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

No publications for rs56730196

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
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs56730196