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dbSNP Short Genetic Variations

Examples: rs268, BRCA1 and more Advanced search

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.

rs3188238

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr6:2948319 (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
G>A
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.000094 (25/264690, TOPMED)
A=0.000060 (15/251156, GnomAD_exome)
A=0.000071 (10/140260, GnomAD) (+ 3 more)
A=0.000066 (8/121096, ExAC)
A=0.00014 (5/36886, ALFA)
A=0.00008 (1/13006, GO-ESP)
Clinical Significance
Reported in ClinVar
Gene : Consequence
SERPINB6 : Synonymous 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: 20231103111315
Population Group Sample Size Ref Allele Alt Allele Ref HMOZ Alt HMOZ HTRZ HWEP
Total Global 53248 G=0.99981 A=0.00019 0.999624 0.0 0.000376 0
European Sub 36686 G=0.99973 A=0.00027 0.999455 0.0 0.000545 0
African Sub 8894 G=1.0000 A=0.0000 1.0 0.0 0.0 N/A
African Others Sub 328 G=1.000 A=0.000 1.0 0.0 0.0 N/A
African American Sub 8566 G=1.0000 A=0.0000 1.0 0.0 0.0 N/A
Asian Sub 116 G=1.000 A=0.000 1.0 0.0 0.0 N/A
East Asian Sub 88 G=1.00 A=0.00 1.0 0.0 0.0 N/A
Other Asian Sub 28 G=1.00 A=0.00 1.0 0.0 0.0 N/A
Latin American 1 Sub 508 G=1.000 A=0.000 1.0 0.0 0.0 N/A
Latin American 2 Sub 634 G=1.000 A=0.000 1.0 0.0 0.0 N/A
South Asian Sub 98 G=1.00 A=0.00 1.0 0.0 0.0 N/A
Other Sub 6312 G=1.0000 A=0.0000 1.0 0.0 0.0 N/A


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 G=0.999906 A=0.000094
gnomAD - Exomes Global Study-wide 251156 G=0.999940 A=0.000060
gnomAD - Exomes European Sub 135132 G=0.999896 A=0.000104
gnomAD - Exomes Asian Sub 49002 G=1.00000 A=0.00000
gnomAD - Exomes American Sub 34588 G=1.00000 A=0.00000
gnomAD - Exomes African Sub 16236 G=0.99994 A=0.00006
gnomAD - Exomes Ashkenazi Jewish Sub 10072 G=1.00000 A=0.00000
gnomAD - Exomes Other Sub 6126 G=1.0000 A=0.0000
gnomAD - Genomes Global Study-wide 140260 G=0.999929 A=0.000071
gnomAD - Genomes European Sub 75960 G=0.99992 A=0.00008
gnomAD - Genomes African Sub 42038 G=0.99998 A=0.00002
gnomAD - Genomes American Sub 13652 G=0.99978 A=0.00022
gnomAD - Genomes Ashkenazi Jewish Sub 3324 G=1.0000 A=0.0000
gnomAD - Genomes East Asian Sub 3134 G=1.0000 A=0.0000
gnomAD - Genomes Other Sub 2152 G=1.0000 A=0.0000
ExAC Global Study-wide 121096 G=0.999934 A=0.000066
ExAC Europe Sub 73126 G=0.99989 A=0.00011
ExAC Asian Sub 25156 G=1.00000 A=0.00000
ExAC American Sub 11564 G=1.00000 A=0.00000
ExAC African Sub 10352 G=1.00000 A=0.00000
ExAC Other Sub 898 G=1.000 A=0.000
Allele Frequency Aggregator Total Global 36886 G=0.99986 A=0.00014
Allele Frequency Aggregator European Sub 26596 G=0.99981 A=0.00019
Allele Frequency Aggregator Other Sub 4878 G=1.0000 A=0.0000
Allele Frequency Aggregator African Sub 4056 G=1.0000 A=0.0000
Allele Frequency Aggregator Latin American 2 Sub 634 G=1.000 A=0.000
Allele Frequency Aggregator Latin American 1 Sub 508 G=1.000 A=0.000
Allele Frequency Aggregator Asian Sub 116 G=1.000 A=0.000
Allele Frequency Aggregator South Asian Sub 98 G=1.00 A=0.00
GO Exome Sequencing Project Global Study-wide 13006 G=0.99992 A=0.00008
GO Exome Sequencing Project European American Sub 8600 G=1.0000 A=0.0000
GO Exome Sequencing Project African American Sub 4406 G=0.9998 A=0.0002
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.p14 chr 6 NC_000006.12:g.2948319G>A
GRCh37.p13 chr 6 NC_000006.11:g.2948553G>A
SERPINB6 RefSeqGene NG_027692.1:g.28847C>T
Gene: SERPINB6, serpin family B member 6 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
SERPINB6 transcript variant 6 NM_001271825.2:c.1110C>T C [TGC] > C [TGT] Coding Sequence Variant
serpin B6 isoform a NP_001258754.1:p.Cys370= C (Cys) > C (Cys) Synonymous Variant
SERPINB6 transcript variant 3 NM_001271822.2:c.1152C>T C [TGC] > C [TGT] Coding Sequence Variant
serpin B6 isoform c NP_001258751.1:p.Cys384= C (Cys) > C (Cys) Synonymous Variant
SERPINB6 transcript variant 10 NM_001374516.1:c.1110C>T C [TGC] > C [TGT] Coding Sequence Variant
serpin B6 isoform a NP_001361445.1:p.Cys370= C (Cys) > C (Cys) Synonymous Variant
SERPINB6 transcript variant 9 NM_001374515.1:c.1122C>T C [TGC] > C [TGT] Coding Sequence Variant
serpin B6 isoform b NP_001361444.1:p.Cys374= C (Cys) > C (Cys) Synonymous Variant
SERPINB6 transcript variant 8 NM_001297700.2:c.1110C>T C [TGC] > C [TGT] Coding Sequence Variant
serpin B6 isoform a NP_001284629.1:p.Cys370= C (Cys) > C (Cys) Synonymous Variant
SERPINB6 transcript variant 7 NM_001297699.2:c.1110C>T C [TGC] > C [TGT] Coding Sequence Variant
serpin B6 isoform a NP_001284628.1:p.Cys370= C (Cys) > C (Cys) Synonymous Variant
SERPINB6 transcript variant 2 NM_001195291.3:c.1122C>T C [TGC] > C [TGT] Coding Sequence Variant
serpin B6 isoform b NP_001182220.2:p.Cys374= C (Cys) > C (Cys) Synonymous Variant
SERPINB6 transcript variant 4 NM_001271823.2:c.1167C>T C [TGC] > C [TGT] Coding Sequence Variant
serpin B6 isoform d NP_001258752.1:p.Cys389= C (Cys) > C (Cys) Synonymous Variant
SERPINB6 transcript variant 1 NM_004568.6:c.1110C>T C [TGC] > C [TGT] Coding Sequence Variant
serpin B6 isoform a NP_004559.4:p.Cys370= C (Cys) > C (Cys) Synonymous Variant
SERPINB6 transcript variant 5 NM_001271824.2:c.1110C>T C [TGC] > C [TGT] Coding Sequence Variant
serpin B6 isoform a NP_001258753.1:p.Cys370= C (Cys) > C (Cys) Synonymous Variant
SERPINB6 transcript variant 11 NM_001374517.1:c.978C>T C [TGC] > C [TGT] Coding Sequence Variant
serpin B6 isoform e NP_001361446.1:p.Cys326= C (Cys) > C (Cys) Synonymous Variant
SERPINB6 transcript variant 12 NR_164657.1:n.1159C>T N/A Non Coding Transcript Variant
SERPINB6 transcript variant X1 XM_047418883.1:c.1344C>T C [TGC] > C [TGT] Coding Sequence Variant
serpin B6 isoform X1 XP_047274839.1:p.Cys448= C (Cys) > C (Cys) Synonymous Variant
SERPINB6 transcript variant X2 XM_011514672.2:c.1344C>T C [TGC] > C [TGT] Coding Sequence Variant
serpin B6 isoform X1 XP_011512974.1:p.Cys448= C (Cys) > C (Cys) Synonymous Variant
SERPINB6 transcript variant X3 XM_047418884.1:c.1344C>T C [TGC] > C [TGT] Coding Sequence Variant
serpin B6 isoform X1 XP_047274840.1:p.Cys448= C (Cys) > C (Cys) Synonymous Variant
SERPINB6 transcript variant X4 XM_047418885.1:c.1344C>T C [TGC] > C [TGT] Coding Sequence Variant
serpin B6 isoform X1 XP_047274841.1:p.Cys448= C (Cys) > C (Cys) Synonymous Variant
SERPINB6 transcript variant X5 XM_047418887.1:c.1344C>T C [TGC] > C [TGT] Coding Sequence Variant
serpin B6 isoform X1 XP_047274843.1:p.Cys448= C (Cys) > C (Cys) Synonymous Variant
SERPINB6 transcript variant X6 XM_047418888.1:c.1344C>T C [TGC] > C [TGT] Coding Sequence Variant
serpin B6 isoform X1 XP_047274844.1:p.Cys448= C (Cys) > C (Cys) Synonymous Variant
SERPINB6 transcript variant X7 XM_047418889.1:c.1122C>T C [TGC] > C [TGT] Coding Sequence Variant
serpin B6 isoform X2 XP_047274845.1:p.Cys374= C (Cys) > C (Cys) Synonymous Variant
SERPINB6 transcript variant X11 XM_047418890.1:c.1122C>T C [TGC] > C [TGT] Coding Sequence Variant
serpin B6 isoform X5 XP_047274846.1:p.Cys374= C (Cys) > C (Cys) Synonymous Variant
SERPINB6 transcript variant X12 XM_047418891.1:c.1110C>T C [TGC] > C [TGT] Coding Sequence Variant
serpin B6 isoform X3 XP_047274847.1:p.Cys370= C (Cys) > C (Cys) Synonymous Variant
SERPINB6 transcript variant X8 XM_047418892.1:c.1110C>T C [TGC] > C [TGT] Coding Sequence Variant
serpin B6 isoform X3 XP_047274848.1:p.Cys370= C (Cys) > C (Cys) Synonymous Variant
SERPINB6 transcript variant X10 XM_017010941.2:c.978C>T C [TGC] > C [TGT] Coding Sequence Variant
serpin B6 isoform X4 XP_016866430.1:p.Cys326= C (Cys) > C (Cys) Synonymous Variant
SERPINB6 transcript variant X9 XM_047418893.1:c.978C>T C [TGC] > C [TGT] Coding Sequence Variant
serpin B6 isoform X4 XP_047274849.1:p.Cys326= C (Cys) > C (Cys) Synonymous Variant
SERPINB6 transcript variant X13 XM_024446465.2:c.978C>T C [TGC] > C [TGT] Coding Sequence Variant
serpin B6 isoform X4 XP_024302233.1:p.Cys326= C (Cys) > C (Cys) Synonymous 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.

Allele: A (allele ID: 655729 )
ClinVar Accession Disease Names Clinical Significance
RCV000827003.4 not provided Likely-Benign
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 G= A
GRCh38.p14 chr 6 NC_000006.12:g.2948319= NC_000006.12:g.2948319G>A
GRCh37.p13 chr 6 NC_000006.11:g.2948553= NC_000006.11:g.2948553G>A
SERPINB6 RefSeqGene NG_027692.1:g.28847= NG_027692.1:g.28847C>T
SERPINB6 transcript variant 1 NM_004568.6:c.1110= NM_004568.6:c.1110C>T
SERPINB6 transcript variant 1 NM_004568.5:c.1110= NM_004568.5:c.1110C>T
SERPINB6 transcript variant 2 NM_001195291.3:c.1122= NM_001195291.3:c.1122C>T
SERPINB6 transcript variant 2 NM_001195291.2:c.1122= NM_001195291.2:c.1122C>T
SERPINB6 transcript variant 4 NM_001271823.2:c.1167= NM_001271823.2:c.1167C>T
SERPINB6 transcript variant 4 NM_001271823.1:c.1167= NM_001271823.1:c.1167C>T
SERPINB6 transcript variant 3 NM_001271822.2:c.1152= NM_001271822.2:c.1152C>T
SERPINB6 transcript variant 3 NM_001271822.1:c.1152= NM_001271822.1:c.1152C>T
SERPINB6 transcript variant 7 NM_001297699.2:c.1110= NM_001297699.2:c.1110C>T
SERPINB6 transcript variant 7 NM_001297699.1:c.1110= NM_001297699.1:c.1110C>T
SERPINB6 transcript variant 6 NM_001271825.2:c.1110= NM_001271825.2:c.1110C>T
SERPINB6 transcript variant 6 NM_001271825.1:c.1110= NM_001271825.1:c.1110C>T
SERPINB6 transcript variant 8 NM_001297700.2:c.1110= NM_001297700.2:c.1110C>T
SERPINB6 transcript variant 8 NM_001297700.1:c.1110= NM_001297700.1:c.1110C>T
SERPINB6 transcript variant 5 NM_001271824.2:c.1110= NM_001271824.2:c.1110C>T
SERPINB6 transcript variant 5 NM_001271824.1:c.1110= NM_001271824.1:c.1110C>T
SERPINB6 transcript variant 9 NM_001374515.1:c.1122= NM_001374515.1:c.1122C>T
SERPINB6 transcript variant 11 NM_001374517.1:c.978= NM_001374517.1:c.978C>T
SERPINB6 transcript variant 12 NR_164657.1:n.1159= NR_164657.1:n.1159C>T
SERPINB6 transcript variant 10 NM_001374516.1:c.1110= NM_001374516.1:c.1110C>T
SERPINB6 transcript variant X10 XM_017010941.2:c.978= XM_017010941.2:c.978C>T
SERPINB6 transcript variant X7 XM_017010941.1:c.978= XM_017010941.1:c.978C>T
SERPINB6 transcript variant X2 XM_011514672.2:c.1344= XM_011514672.2:c.1344C>T
SERPINB6 transcript variant X1 XM_011514672.1:c.1344= XM_011514672.1:c.1344C>T
SERPINB6 transcript variant X13 XM_024446465.2:c.978= XM_024446465.2:c.978C>T
SERPINB6 transcript variant X9 XM_024446465.1:c.978= XM_024446465.1:c.978C>T
SERPINB6 transcript variant X1 XM_047418883.1:c.1344= XM_047418883.1:c.1344C>T
SERPINB6 transcript variant X7 XM_047418889.1:c.1122= XM_047418889.1:c.1122C>T
SERPINB6 transcript variant X11 XM_047418890.1:c.1122= XM_047418890.1:c.1122C>T
SERPINB6 transcript variant X12 XM_047418891.1:c.1110= XM_047418891.1:c.1110C>T
SERPINB6 transcript variant X3 XM_047418884.1:c.1344= XM_047418884.1:c.1344C>T
SERPINB6 transcript variant X5 XM_047418887.1:c.1344= XM_047418887.1:c.1344C>T
SERPINB6 transcript variant X4 XM_047418885.1:c.1344= XM_047418885.1:c.1344C>T
SERPINB6 transcript variant X8 XM_047418892.1:c.1110= XM_047418892.1:c.1110C>T
SERPINB6 transcript variant X6 XM_047418888.1:c.1344= XM_047418888.1:c.1344C>T
SERPINB6 transcript variant X9 XM_047418893.1:c.978= XM_047418893.1:c.978C>T
serpin B6 isoform a NP_004559.4:p.Cys370= NP_004559.4:p.Cys370=
serpin B6 isoform b NP_001182220.2:p.Cys374= NP_001182220.2:p.Cys374=
serpin B6 isoform d NP_001258752.1:p.Cys389= NP_001258752.1:p.Cys389=
serpin B6 isoform c NP_001258751.1:p.Cys384= NP_001258751.1:p.Cys384=
serpin B6 isoform a NP_001284628.1:p.Cys370= NP_001284628.1:p.Cys370=
serpin B6 isoform a NP_001258754.1:p.Cys370= NP_001258754.1:p.Cys370=
serpin B6 isoform a NP_001284629.1:p.Cys370= NP_001284629.1:p.Cys370=
serpin B6 isoform a NP_001258753.1:p.Cys370= NP_001258753.1:p.Cys370=
serpin B6 isoform b NP_001361444.1:p.Cys374= NP_001361444.1:p.Cys374=
serpin B6 isoform e NP_001361446.1:p.Cys326= NP_001361446.1:p.Cys326=
serpin B6 isoform a NP_001361445.1:p.Cys370= NP_001361445.1:p.Cys370=
serpin B6 isoform X4 XP_016866430.1:p.Cys326= XP_016866430.1:p.Cys326=
serpin B6 isoform X1 XP_011512974.1:p.Cys448= XP_011512974.1:p.Cys448=
serpin B6 isoform X4 XP_024302233.1:p.Cys326= XP_024302233.1:p.Cys326=
serpin B6 isoform X1 XP_047274839.1:p.Cys448= XP_047274839.1:p.Cys448=
serpin B6 isoform X2 XP_047274845.1:p.Cys374= XP_047274845.1:p.Cys374=
serpin B6 isoform X5 XP_047274846.1:p.Cys374= XP_047274846.1:p.Cys374=
serpin B6 isoform X3 XP_047274847.1:p.Cys370= XP_047274847.1:p.Cys370=
serpin B6 isoform X1 XP_047274840.1:p.Cys448= XP_047274840.1:p.Cys448=
serpin B6 isoform X1 XP_047274843.1:p.Cys448= XP_047274843.1:p.Cys448=
serpin B6 isoform X1 XP_047274841.1:p.Cys448= XP_047274841.1:p.Cys448=
serpin B6 isoform X3 XP_047274848.1:p.Cys370= XP_047274848.1:p.Cys370=
serpin B6 isoform X1 XP_047274844.1:p.Cys448= XP_047274844.1:p.Cys448=
serpin B6 isoform X4 XP_047274849.1:p.Cys326= XP_047274849.1:p.Cys326=
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#.

20 SubSNP, 6 Frequency, 1 ClinVar submissions
No Submitter Submission ID Date (Build)
1 LEE ss4412664 May 29, 2002 (105)
2 ILLUMINA ss75178914 Dec 07, 2007 (129)
3 KRIBB_YJKIM ss119456078 Dec 01, 2009 (131)
4 ILLUMINA ss173573008 Jul 04, 2010 (132)
5 NHLBI-ESP ss342200105 May 09, 2011 (134)
6 ILLUMINA ss537167273 Sep 08, 2015 (146)
7 EVA_DECODE ss1592061521 Apr 01, 2015 (144)
8 EVA_EXAC ss1688140361 Apr 01, 2015 (144)
9 HUMAN_LONGEVITY ss2281271533 Dec 20, 2016 (150)
10 GNOMAD ss2735510819 Nov 08, 2017 (151)
11 GNOMAD ss2747538062 Nov 08, 2017 (151)
12 GNOMAD ss2835087156 Nov 08, 2017 (151)
13 ILLUMINA ss3629428045 Oct 12, 2018 (152)
14 ILLUMINA ss3638602950 Oct 12, 2018 (152)
15 ILLUMINA ss3643545146 Oct 12, 2018 (152)
16 EVA_DECODE ss3716454912 Jul 13, 2019 (153)
17 EVA ss3824151587 Apr 26, 2020 (154)
18 EVA ss4017251386 Apr 26, 2021 (155)
19 TOPMED ss4691572730 Apr 26, 2021 (155)
20 HUGCELL_USP ss5464990486 Oct 13, 2022 (156)
21 ExAC NC_000006.11 - 2948553 Oct 12, 2018 (152)
22 gnomAD - Genomes NC_000006.12 - 2948319 Apr 26, 2021 (155)
23 gnomAD - Exomes NC_000006.11 - 2948553 Jul 13, 2019 (153)
24 GO Exome Sequencing Project NC_000006.11 - 2948553 Oct 12, 2018 (152)
25 TopMed NC_000006.12 - 2948319 Apr 26, 2021 (155)
26 ALFA NC_000006.12 - 2948319 Apr 26, 2021 (155)
27 ClinVar RCV000827003.4 Oct 13, 2022 (156)
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)
rs386580635 Aug 21, 2014 (142)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss1592061521, ss3643545146 NC_000006.10:2893551:G:A NC_000006.12:2948318:G:A (self)
8157626, 4645939, 609644, ss342200105, ss537167273, ss1688140361, ss2735510819, ss2747538062, ss2835087156, ss3629428045, ss3638602950, ss3824151587, ss4017251386 NC_000006.11:2948552:G:A NC_000006.12:2948318:G:A (self)
RCV000827003.4, 215318251, 528950288, 14131962377, ss2281271533, ss3716454912, ss4691572730, ss5464990486 NC_000006.12:2948318:G:A NC_000006.12:2948318:G:A (self)
ss4412664, ss75178914, ss119456078, ss173573008 NT_007592.15:2888552:G:A NC_000006.12:2948318:G:A (self)
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 rs3188238

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.post820+afb47a3d