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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.

rs781743659

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr16:15006485-15006489 (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
delTCGT
Variation Type
Indel Insertion and Deletion
Frequency
delTCGT=0.000011 (3/264690, TOPMED)
delTCGT=0.000008 (1/121402, ExAC)
delTCGT=0.00000 (0/11862, ALFA)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
PDXDC1 : Stop Gained
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 16 NC_000016.10:g.15006486_15006489del
GRCh37.p13 chr 16 NC_000016.9:g.15100343_15100346del
GRCh38.p13 chr 16 alt locus HSCHR16_1_CTG1 NT_187607.1:g.845839_845842del
Gene: PDXDC1, pyridoxal dependent decarboxylase domain containing 1 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
PDXDC1 transcript variant 5 NM_001285448.1:c.209_212d…

NM_001285448.1:c.209_212del

F [TTC] > * [TA] Coding Sequence Variant
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform 5 NP_001272377.1:p.Asp69_Ph…

NP_001272377.1:p.Asp69_Phe70insTer

F (Phe) > * (Ter) Stop Gained
PDXDC1 transcript variant 4 NM_001285447.1:c.437_440d…

NM_001285447.1:c.437_440del

F [TTC] > * [TA] Coding Sequence Variant
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform 4 NP_001272376.1:p.Asp145_P…

NP_001272376.1:p.Asp145_Phe146insTer

F (Phe) > * (Ter) Stop Gained
PDXDC1 transcript variant 1 NM_015027.4:c.482_485del F [TTC] > * [TA] Coding Sequence Variant
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform 1 NP_055842.2:p.Asp160_Phe1…

NP_055842.2:p.Asp160_Phe161insTer

F (Phe) > * (Ter) Stop Gained
PDXDC1 transcript variant 7 NM_001285450.2:c.482_485d…

NM_001285450.2:c.482_485del

F [TTC] > * [TA] Coding Sequence Variant
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform 7 NP_001272379.1:p.Asp160_P…

NP_001272379.1:p.Asp160_Phe161insTer

F (Phe) > * (Ter) Stop Gained
PDXDC1 transcript variant 3 NM_001285445.2:c.398_401d…

NM_001285445.2:c.398_401del

F [TTC] > * [TA] Coding Sequence Variant
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform 3 NP_001272374.1:p.Asp132_P…

NP_001272374.1:p.Asp132_Phe133insTer

F (Phe) > * (Ter) Stop Gained
PDXDC1 transcript variant 2 NM_001285444.2:c.401_404d…

NM_001285444.2:c.401_404del

F [TTC] > * [TA] Coding Sequence Variant
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform 2 NP_001272373.1:p.Asp133_P…

NP_001272373.1:p.Asp133_Phe134insTer

F (Phe) > * (Ter) Stop Gained
PDXDC1 transcript variant 8 NM_001324019.2:c.479_482d…

NM_001324019.2:c.479_482del

F [TTC] > * [TA] Coding Sequence Variant
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform 8 NP_001310948.1:p.Asp159_P…

NP_001310948.1:p.Asp159_Phe160insTer

F (Phe) > * (Ter) Stop Gained
PDXDC1 transcript variant 9 NM_001324020.2:c.479_482d…

NM_001324020.2:c.479_482del

F [TTC] > * [TA] Coding Sequence Variant
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform 9 NP_001310949.1:p.Asp159_P…

NP_001310949.1:p.Asp159_Phe160insTer

F (Phe) > * (Ter) Stop Gained
PDXDC1 transcript variant 10 NM_001324021.2:c.401_404d…

NM_001324021.2:c.401_404del

F [TTC] > * [TA] Coding Sequence Variant
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform 10 NP_001310950.1:p.Asp133_P…

NP_001310950.1:p.Asp133_Phe134insTer

F (Phe) > * (Ter) Stop Gained
PDXDC1 transcript variant 6 NM_001285449.2:c.482_485d…

NM_001285449.2:c.482_485del

F [TTC] > * [TA] Coding Sequence Variant
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform 6 NP_001272378.1:p.Asp160_P…

NP_001272378.1:p.Asp160_Phe161insTer

F (Phe) > * (Ter) Stop Gained
PDXDC1 transcript variant X4 XM_006720865.2:c.356_359d…

XM_006720865.2:c.356_359del

F [TTC] > * [TA] Coding Sequence Variant
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X4 XP_006720928.2:p.Asp118_P…

XP_006720928.2:p.Asp118_Phe119insTer

F (Phe) > * (Ter) Stop Gained
PDXDC1 transcript variant X1 XM_017023059.1:c.437_440d…

XM_017023059.1:c.437_440del

F [TTC] > * [TA] Coding Sequence Variant
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X1 XP_016878548.1:p.Asp145_P…

XP_016878548.1:p.Asp145_Phe146insTer

F (Phe) > * (Ter) Stop Gained
PDXDC1 transcript variant X3 XM_017023060.1:c.509_512d…

XM_017023060.1:c.509_512del

F [TTC] > * [TA] Coding Sequence Variant
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X3 XP_016878549.1:p.Asp169_P…

XP_016878549.1:p.Asp169_Phe170insTer

F (Phe) > * (Ter) Stop Gained
PDXDC1 transcript variant X7 XM_017023062.1:c.437_440d…

XM_017023062.1:c.437_440del

F [TTC] > * [TA] Coding Sequence Variant
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X1 XP_016878551.1:p.Asp145_P…

XP_016878551.1:p.Asp145_Phe146insTer

F (Phe) > * (Ter) Stop Gained
PDXDC1 transcript variant X8 XM_017023063.1:c.437_440d…

XM_017023063.1:c.437_440del

F [TTC] > * [TA] Coding Sequence Variant
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X5 XP_016878552.1:p.Asp145_P…

XP_016878552.1:p.Asp145_Phe146insTer

F (Phe) > * (Ter) Stop Gained
PDXDC1 transcript variant X9 XM_017023064.1:c.356_359d…

XM_017023064.1:c.356_359del

F [TTC] > * [TA] Coding Sequence Variant
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X4 XP_016878553.1:p.Asp118_P…

XP_016878553.1:p.Asp118_Phe119insTer

F (Phe) > * (Ter) Stop Gained
PDXDC1 transcript variant X10 XM_017023065.1:c.437_440d…

XM_017023065.1:c.437_440del

F [TTC] > * [TA] Coding Sequence Variant
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X6 XP_016878554.1:p.Asp145_P…

XP_016878554.1:p.Asp145_Phe146insTer

F (Phe) > * (Ter) Stop Gained
PDXDC1 transcript variant X5 XM_005255176.3:c.437_440d…

XM_005255176.3:c.437_440del

F [TTC] > * [TA] Coding Sequence Variant
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X1 XP_005255233.1:p.Asp145_P…

XP_005255233.1:p.Asp145_Phe146insTer

F (Phe) > * (Ter) Stop Gained
PDXDC1 transcript variant X6 XM_017023061.2:c.437_440d…

XM_017023061.2:c.437_440del

F [TTC] > * [TA] Coding Sequence Variant
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X1 XP_016878550.1:p.Asp145_P…

XP_016878550.1:p.Asp145_Phe146insTer

F (Phe) > * (Ter) Stop Gained
PDXDC1 transcript variant X11 XM_024450194.1:c.437_440d…

XM_024450194.1:c.437_440del

F [TTC] > * [TA] Coding Sequence Variant
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X7 XP_024305962.1:p.Asp145_P…

XP_024305962.1:p.Asp145_Phe146insTer

F (Phe) > * (Ter) Stop Gained
PDXDC1 transcript variant X12 XM_024450195.1:c.536_539d…

XM_024450195.1:c.536_539del

F [TTC] > * [TA] Coding Sequence Variant
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X8 XP_024305963.1:p.Asp178_P…

XP_024305963.1:p.Asp178_Phe179insTer

F (Phe) > * (Ter) Stop Gained
PDXDC1 transcript variant X13 XM_024450196.1:c.509_512d…

XM_024450196.1:c.509_512del

F [TTC] > * [TA] Coding Sequence Variant
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X9 XP_024305964.1:p.Asp169_P…

XP_024305964.1:p.Asp169_Phe170insTer

F (Phe) > * (Ter) Stop Gained
PDXDC1 transcript variant X14 XM_024450197.1:c.356_359d…

XM_024450197.1:c.356_359del

F [TTC] > * [TA] Coding Sequence Variant
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X10 XP_024305965.1:p.Asp118_P…

XP_024305965.1:p.Asp118_Phe119insTer

F (Phe) > * (Ter) Stop Gained
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 11862 TTCGT=1.00000 T=0.00000
European Sub 7618 TTCGT=1.0000 T=0.0000
African Sub 2816 TTCGT=1.0000 T=0.0000
African Others Sub 108 TTCGT=1.000 T=0.000
African American Sub 2708 TTCGT=1.0000 T=0.0000
Asian Sub 108 TTCGT=1.000 T=0.000
East Asian Sub 84 TTCGT=1.00 T=0.00
Other Asian Sub 24 TTCGT=1.00 T=0.00
Latin American 1 Sub 146 TTCGT=1.000 T=0.000
Latin American 2 Sub 610 TTCGT=1.000 T=0.000
South Asian Sub 94 TTCGT=1.00 T=0.00
Other Sub 470 TTCGT=1.000 T=0.000


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
TopMed Global Study-wide 264690 TTCGT=0.999989 delTCGT=0.000011
ExAC Global Study-wide 121402 TTCGT=0.999992 delTCGT=0.000008
ExAC Europe Sub 73352 TTCGT=0.99999 delTCGT=0.00001
ExAC Asian Sub 25158 TTCGT=1.00000 delTCGT=0.00000
ExAC American Sub 11578 TTCGT=1.00000 delTCGT=0.00000
ExAC African Sub 10406 TTCGT=1.00000 delTCGT=0.00000
ExAC Other Sub 908 TTCGT=1.000 delTCGT=0.000
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 TTCGT= delTCGT
GRCh38.p13 chr 16 NC_000016.10:g.15006485_15006489= NC_000016.10:g.15006486_15006489del
GRCh37.p13 chr 16 NC_000016.9:g.15100342_15100346= NC_000016.9:g.15100343_15100346del
GRCh38.p13 chr 16 alt locus HSCHR16_1_CTG1 NT_187607.1:g.845838_845842= NT_187607.1:g.845839_845842del
PDXDC1 transcript variant 1 NM_015027.4:c.481_485= NM_015027.4:c.482_485del
PDXDC1 transcript variant 1 NM_015027.3:c.481_485= NM_015027.3:c.482_485del
PDXDC1 transcript NM_015027.2:c.481_485= NM_015027.2:c.482_485del
PDXDC1 transcript variant X5 XM_005255176.3:c.436_440= XM_005255176.3:c.437_440del
PDXDC1 transcript variant X4 XM_005255176.1:c.436_440= XM_005255176.1:c.437_440del
PDXDC1 transcript variant 8 NM_001324019.2:c.478_482= NM_001324019.2:c.479_482del
PDXDC1 transcript variant 8 NM_001324019.1:c.478_482= NM_001324019.1:c.479_482del
PDXDC1 transcript variant 2 NM_001285444.2:c.400_404= NM_001285444.2:c.401_404del
PDXDC1 transcript variant 2 NM_001285444.1:c.400_404= NM_001285444.1:c.401_404del
PDXDC1 transcript variant 3 NM_001285445.2:c.397_401= NM_001285445.2:c.398_401del
PDXDC1 transcript variant 3 NM_001285445.1:c.397_401= NM_001285445.1:c.398_401del
PDXDC1 transcript variant X6 XM_017023061.2:c.436_440= XM_017023061.2:c.437_440del
PDXDC1 transcript variant X4 XM_006720865.2:c.355_359= XM_006720865.2:c.356_359del
PDXDC1 transcript variant 7 NM_001285450.2:c.481_485= NM_001285450.2:c.482_485del
PDXDC1 transcript variant 7 NM_001285450.1:c.481_485= NM_001285450.1:c.482_485del
PDXDC1 transcript variant 6 NM_001285449.2:c.481_485= NM_001285449.2:c.482_485del
PDXDC1 transcript variant 6 NM_001285449.1:c.481_485= NM_001285449.1:c.482_485del
PDXDC1 transcript variant 9 NM_001324020.2:c.478_482= NM_001324020.2:c.479_482del
PDXDC1 transcript variant 9 NM_001324020.1:c.478_482= NM_001324020.1:c.479_482del
PDXDC1 transcript variant 10 NM_001324021.2:c.400_404= NM_001324021.2:c.401_404del
PDXDC1 transcript variant 10 NM_001324021.1:c.400_404= NM_001324021.1:c.401_404del
PDXDC1 transcript variant X10 XM_017023065.1:c.436_440= XM_017023065.1:c.437_440del
PDXDC1 transcript variant 5 NM_001285448.1:c.208_212= NM_001285448.1:c.209_212del
PDXDC1 transcript variant 4 NM_001285447.1:c.436_440= NM_001285447.1:c.437_440del
PDXDC1 transcript variant X9 XM_017023064.1:c.355_359= XM_017023064.1:c.356_359del
PDXDC1 transcript variant X13 XM_024450196.1:c.508_512= XM_024450196.1:c.509_512del
PDXDC1 transcript variant X12 XM_024450195.1:c.535_539= XM_024450195.1:c.536_539del
PDXDC1 transcript variant X14 XM_024450197.1:c.355_359= XM_024450197.1:c.356_359del
PDXDC1 transcript variant X11 XM_024450194.1:c.436_440= XM_024450194.1:c.437_440del
PDXDC1 transcript variant X3 XM_017023060.1:c.508_512= XM_017023060.1:c.509_512del
PDXDC1 transcript variant X8 XM_017023063.1:c.436_440= XM_017023063.1:c.437_440del
PDXDC1 transcript variant X7 XM_017023062.1:c.436_440= XM_017023062.1:c.437_440del
PDXDC1 transcript variant X1 XM_017023059.1:c.436_440= XM_017023059.1:c.437_440del
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform 1 NP_055842.2:p.Phe161_Val162= NP_055842.2:p.Asp160_Phe161insTer
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X1 XP_005255233.1:p.Phe146_Val147= XP_005255233.1:p.Asp145_Phe146insTer
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform 8 NP_001310948.1:p.Phe160_Val161= NP_001310948.1:p.Asp159_Phe160insTer
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform 2 NP_001272373.1:p.Phe134_Val135= NP_001272373.1:p.Asp133_Phe134insTer
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform 3 NP_001272374.1:p.Phe133_Val134= NP_001272374.1:p.Asp132_Phe133insTer
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X1 XP_016878550.1:p.Phe146_Val147= XP_016878550.1:p.Asp145_Phe146insTer
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X4 XP_006720928.2:p.Phe119_Val120= XP_006720928.2:p.Asp118_Phe119insTer
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform 7 NP_001272379.1:p.Phe161_Val162= NP_001272379.1:p.Asp160_Phe161insTer
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform 6 NP_001272378.1:p.Phe161_Val162= NP_001272378.1:p.Asp160_Phe161insTer
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform 9 NP_001310949.1:p.Phe160_Val161= NP_001310949.1:p.Asp159_Phe160insTer
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform 10 NP_001310950.1:p.Phe134_Val135= NP_001310950.1:p.Asp133_Phe134insTer
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X6 XP_016878554.1:p.Phe146_Val147= XP_016878554.1:p.Asp145_Phe146insTer
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform 5 NP_001272377.1:p.Phe70_Val71= NP_001272377.1:p.Asp69_Phe70insTer
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform 4 NP_001272376.1:p.Phe146_Val147= NP_001272376.1:p.Asp145_Phe146insTer
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X4 XP_016878553.1:p.Phe119_Val120= XP_016878553.1:p.Asp118_Phe119insTer
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X9 XP_024305964.1:p.Phe170_Val171= XP_024305964.1:p.Asp169_Phe170insTer
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X8 XP_024305963.1:p.Phe179_Val180= XP_024305963.1:p.Asp178_Phe179insTer
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X10 XP_024305965.1:p.Phe119_Val120= XP_024305965.1:p.Asp118_Phe119insTer
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X7 XP_024305962.1:p.Phe146_Val147= XP_024305962.1:p.Asp145_Phe146insTer
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X3 XP_016878549.1:p.Phe170_Val171= XP_016878549.1:p.Asp169_Phe170insTer
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X5 XP_016878552.1:p.Phe146_Val147= XP_016878552.1:p.Asp145_Phe146insTer
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X1 XP_016878551.1:p.Phe146_Val147= XP_016878551.1:p.Asp145_Phe146insTer
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X1 XP_016878548.1:p.Phe146_Val147= XP_016878548.1:p.Asp145_Phe146insTer
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#.

3 SubSNP, 3 Frequency submissions
No Submitter Submission ID Date (Build)
1 EVA_EXAC ss1712101798 Apr 01, 2015 (144)
2 TOPMED ss3241242288 Nov 08, 2017 (151)
3 TOPMED ss5009298687 Apr 26, 2021 (155)
4 ExAC NC_000016.9 - 15100342 Oct 12, 2018 (152)
5 TopMed NC_000016.10 - 15006485 Apr 26, 2021 (155)
6 ALFA NC_000016.10 - 15006485 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).

Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
2565531, ss1712101798 NC_000016.9:15100341:TTCG: NC_000016.10:15006484:TTCGT:T (self)
224844348, ss3241242288, ss5009298687 NC_000016.10:15006484:TTCG: NC_000016.10:15006484:TTCGT:T (self)
3514307901 NC_000016.10:15006484:TTCGT:T NC_000016.10:15006484:TTCGT:T
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 rs781743659

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