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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.

rs112690643

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr1:1184019 (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
C>T
Variation Type
SNV Single Nucleotide Variation
Frequency
T=0.008240 (2181/264690, TOPMED)
T=0.002076 (522/251480, GnomAD_exome)
T=0.007892 (1107/140266, GnomAD) (+ 14 more)
T=0.002710 (329/121402, ExAC)
T=0.01216 (957/78698, PAGE_STUDY)
T=0.00258 (118/45750, ALFA)
T=0.00011 (3/28258, 14KJPN)
T=0.00006 (1/16760, 8.3KJPN)
T=0.00830 (108/13006, GO-ESP)
T=0.0069 (44/6404, 1000G_30x)
T=0.0064 (32/5008, 1000G)
T=0.0003 (1/3854, ALSPAC)
T=0.0000 (0/3708, TWINSUK)
T=0.002 (1/534, MGP)
T=0.009 (2/216, Qatari)
C=0.5 (5/10, SGDP_PRJ)
T=0.5 (5/10, SGDP_PRJ)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
TTLL10 : 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: 20230706150541
Population Group Sample Size Ref Allele Alt Allele
Total Global 62112 C=0.99609 T=0.00391
European Sub 42952 C=0.99984 T=0.00016
African Sub 8856 C=0.9753 T=0.0247
African Others Sub 306 C=0.951 T=0.049
African American Sub 8550 C=0.9761 T=0.0239
Asian Sub 206 C=1.000 T=0.000
East Asian Sub 148 C=1.000 T=0.000
Other Asian Sub 58 C=1.00 T=0.00
Latin American 1 Sub 508 C=0.998 T=0.002
Latin American 2 Sub 634 C=1.000 T=0.000
South Asian Sub 104 C=1.000 T=0.000
Other Sub 8852 C=0.9982 T=0.0018


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 C=0.991760 T=0.008240
gnomAD - Exomes Global Study-wide 251480 C=0.997924 T=0.002076
gnomAD - Exomes European Sub 135408 C=0.999778 T=0.000222
gnomAD - Exomes Asian Sub 49010 C=0.99994 T=0.00006
gnomAD - Exomes American Sub 34590 C=0.99780 T=0.00220
gnomAD - Exomes African Sub 16254 C=0.97539 T=0.02461
gnomAD - Exomes Ashkenazi Jewish Sub 10080 C=0.99990 T=0.00010
gnomAD - Exomes Other Sub 6138 C=0.9980 T=0.0020
gnomAD - Genomes Global Study-wide 140266 C=0.992108 T=0.007892
gnomAD - Genomes European Sub 75958 C=0.99978 T=0.00022
gnomAD - Genomes African Sub 42042 C=0.97514 T=0.02486
gnomAD - Genomes American Sub 13656 C=0.99810 T=0.00190
gnomAD - Genomes Ashkenazi Jewish Sub 3324 C=1.0000 T=0.0000
gnomAD - Genomes East Asian Sub 3132 C=1.0000 T=0.0000
gnomAD - Genomes Other Sub 2154 C=0.9912 T=0.0088
ExAC Global Study-wide 121402 C=0.997290 T=0.002710
ExAC Europe Sub 73350 C=0.99967 T=0.00033
ExAC Asian Sub 25166 C=0.99996 T=0.00004
ExAC American Sub 11578 C=0.99715 T=0.00285
ExAC African Sub 10402 C=0.97404 T=0.02596
ExAC Other Sub 906 C=0.999 T=0.001
The PAGE Study Global Study-wide 78698 C=0.98784 T=0.01216
The PAGE Study AfricanAmerican Sub 32514 C=0.97552 T=0.02448
The PAGE Study Mexican Sub 10810 C=0.99861 T=0.00139
The PAGE Study Asian Sub 8318 C=0.9999 T=0.0001
The PAGE Study PuertoRican Sub 7918 C=0.9936 T=0.0064
The PAGE Study NativeHawaiian Sub 4534 C=0.9996 T=0.0004
The PAGE Study Cuban Sub 4228 C=0.9922 T=0.0078
The PAGE Study Dominican Sub 3828 C=0.9901 T=0.0099
The PAGE Study CentralAmerican Sub 2450 C=0.9963 T=0.0037
The PAGE Study SouthAmerican Sub 1982 C=0.9980 T=0.0020
The PAGE Study NativeAmerican Sub 1260 C=0.9944 T=0.0056
The PAGE Study SouthAsian Sub 856 C=0.999 T=0.001
Allele Frequency Aggregator Total Global 45750 C=0.99742 T=0.00258
Allele Frequency Aggregator European Sub 32862 C=0.99982 T=0.00018
Allele Frequency Aggregator Other Sub 7418 C=0.9988 T=0.0012
Allele Frequency Aggregator African Sub 4018 C=0.9746 T=0.0254
Allele Frequency Aggregator Latin American 2 Sub 634 C=1.000 T=0.000
Allele Frequency Aggregator Latin American 1 Sub 508 C=0.998 T=0.002
Allele Frequency Aggregator Asian Sub 206 C=1.000 T=0.000
Allele Frequency Aggregator South Asian Sub 104 C=1.000 T=0.000
14KJPN JAPANESE Study-wide 28258 C=0.99989 T=0.00011
8.3KJPN JAPANESE Study-wide 16760 C=0.99994 T=0.00006
GO Exome Sequencing Project Global Study-wide 13006 C=0.99170 T=0.00830
GO Exome Sequencing Project European American Sub 8600 C=1.0000 T=0.0000
GO Exome Sequencing Project African American Sub 4406 C=0.9755 T=0.0245
1000Genomes_30x Global Study-wide 6404 C=0.9931 T=0.0069
1000Genomes_30x African Sub 1786 C=0.9759 T=0.0241
1000Genomes_30x Europe Sub 1266 C=1.0000 T=0.0000
1000Genomes_30x South Asian Sub 1202 C=1.0000 T=0.0000
1000Genomes_30x East Asian Sub 1170 C=1.0000 T=0.0000
1000Genomes_30x American Sub 980 C=0.999 T=0.001
1000Genomes Global Study-wide 5008 C=0.9936 T=0.0064
1000Genomes African Sub 1322 C=0.9766 T=0.0234
1000Genomes East Asian Sub 1008 C=1.0000 T=0.0000
1000Genomes Europe Sub 1006 C=1.0000 T=0.0000
1000Genomes South Asian Sub 978 C=1.000 T=0.000
1000Genomes American Sub 694 C=0.999 T=0.001
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 C=0.9997 T=0.0003
UK 10K study - Twins TWIN COHORT Study-wide 3708 C=1.0000 T=0.0000
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 C=0.998 T=0.002
Qatari Global Study-wide 216 C=0.991 T=0.009
SGDP_PRJ Global Study-wide 10 C=0.5 T=0.5
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 1 NC_000001.11:g.1184019C>T
GRCh37.p13 chr 1 NC_000001.10:g.1119399C>T
Gene: TTLL10, tubulin tyrosine ligase like 10 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
TTLL10 transcript variant 2 NM_153254.3:c.969C>T H [CAC] > H [CAT] Coding Sequence Variant
inactive polyglycylase TTLL10 isoform 2 NP_694986.2:p.His323= H (His) > H (His) Synonymous Variant
TTLL10 transcript variant 1 NM_001130045.2:c.1188C>T H [CAC] > H [CAT] Coding Sequence Variant
inactive polyglycylase TTLL10 isoform 1 NP_001123517.1:p.His396= H (His) > H (His) Synonymous Variant
TTLL10 transcript variant 3 NM_001371649.1:c.1188C>T H [CAC] > H [CAT] Coding Sequence Variant
inactive polyglycylase TTLL10 isoform 1 NP_001358578.1:p.His396= H (His) > H (His) Synonymous Variant
TTLL10 transcript variant X1 XM_047416841.1:c.1566C>T H [CAC] > H [CAT] Coding Sequence Variant
inactive polyglycylase TTLL10 isoform X1 XP_047272797.1:p.His522= H (His) > H (His) Synonymous Variant
TTLL10 transcript variant X2 XM_017000906.2:c.1485C>T H [CAC] > H [CAT] Coding Sequence Variant
inactive polyglycylase TTLL10 isoform X2 XP_016856395.2:p.His495= H (His) > H (His) Synonymous Variant
TTLL10 transcript variant X3 XM_047416842.1:c.1476C>T H [CAC] > H [CAT] Coding Sequence Variant
inactive polyglycylase TTLL10 isoform X3 XP_047272798.1:p.His492= H (His) > H (His) Synonymous Variant
TTLL10 transcript variant X4 XM_047416843.1:c.1566C>T H [CAC] > H [CAT] Coding Sequence Variant
inactive polyglycylase TTLL10 isoform X1 XP_047272799.1:p.His522= H (His) > H (His) Synonymous Variant
TTLL10 transcript variant X5 XM_017000907.2:c.1566C>T H [CAC] > H [CAT] Coding Sequence Variant
inactive polyglycylase TTLL10 isoform X4 XP_016856396.2:p.His522= H (His) > H (His) Synonymous Variant
TTLL10 transcript variant X6 XM_017000908.2:c.1566C>T H [CAC] > H [CAT] Coding Sequence Variant
inactive polyglycylase TTLL10 isoform X5 XP_016856397.2:p.His522= H (His) > H (His) Synonymous Variant
TTLL10 transcript variant X7 XM_017000909.2:c.1566C>T H [CAC] > H [CAT] Coding Sequence Variant
inactive polyglycylase TTLL10 isoform X6 XP_016856398.2:p.His522= H (His) > H (His) Synonymous Variant
TTLL10 transcript variant X8 XM_017000910.3:c.1566C>T H [CAC] > H [CAT] Coding Sequence Variant
inactive polyglycylase TTLL10 isoform X7 XP_016856399.2:p.His522= H (His) > H (His) Synonymous Variant
TTLL10 transcript variant X9 XM_047416870.1:c.1188C>T H [CAC] > H [CAT] Coding Sequence Variant
inactive polyglycylase TTLL10 isoform X8 XP_047272826.1:p.His396= H (His) > H (His) Synonymous Variant
TTLL10 transcript variant X10 XM_017000912.2:c.1188C>T H [CAC] > H [CAT] Coding Sequence Variant
inactive polyglycylase TTLL10 isoform X8 XP_016856401.1:p.His396= H (His) > H (His) Synonymous Variant
TTLL10 transcript variant X11 XM_047416882.1:c.1566C>T H [CAC] > H [CAT] Coding Sequence Variant
inactive polyglycylase TTLL10 isoform X9 XP_047272838.1:p.His522= H (His) > H (His) Synonymous Variant
TTLL10 transcript variant X12 XM_005244738.2:c.969C>T H [CAC] > H [CAT] Coding Sequence Variant
inactive polyglycylase TTLL10 isoform X10 XP_005244795.1:p.His323= H (His) > H (His) 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.

Not Reported in ClinVar
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 C= T
GRCh38.p14 chr 1 NC_000001.11:g.1184019= NC_000001.11:g.1184019C>T
GRCh37.p13 chr 1 NC_000001.10:g.1119399= NC_000001.10:g.1119399C>T
TTLL10 transcript variant X8 XM_017000910.3:c.1566= XM_017000910.3:c.1566C>T
TTLL10 transcript variant X5 XM_017000910.2:c.1188= XM_017000910.2:c.1188C>T
TTLL10 transcript variant X5 XM_017000910.1:c.1188= XM_017000910.1:c.1188C>T
TTLL10 transcript variant 2 NM_153254.3:c.969= NM_153254.3:c.969C>T
TTLL10 transcript variant 2 NM_153254.2:c.969= NM_153254.2:c.969C>T
TTLL10 transcript variant X2 XM_017000906.2:c.1485= XM_017000906.2:c.1485C>T
TTLL10 transcript variant X1 XM_017000906.1:c.1107= XM_017000906.1:c.1107C>T
TTLL10 transcript variant X7 XM_017000909.2:c.1566= XM_017000909.2:c.1566C>T
TTLL10 transcript variant X4 XM_017000909.1:c.1188= XM_017000909.1:c.1188C>T
TTLL10 transcript variant X10 XM_017000912.2:c.1188= XM_017000912.2:c.1188C>T
TTLL10 transcript variant X8 XM_017000912.1:c.1188= XM_017000912.1:c.1188C>T
TTLL10 transcript variant 1 NM_001130045.2:c.1188= NM_001130045.2:c.1188C>T
TTLL10 transcript variant 1 NM_001130045.1:c.1188= NM_001130045.1:c.1188C>T
TTLL10 transcript variant X5 XM_017000907.2:c.1566= XM_017000907.2:c.1566C>T
TTLL10 transcript variant X2 XM_017000907.1:c.1188= XM_017000907.1:c.1188C>T
TTLL10 transcript variant X6 XM_017000908.2:c.1566= XM_017000908.2:c.1566C>T
TTLL10 transcript variant X3 XM_017000908.1:c.1188= XM_017000908.1:c.1188C>T
TTLL10 transcript variant X12 XM_005244738.2:c.969= XM_005244738.2:c.969C>T
TTLL10 transcript variant X10 XM_005244738.1:c.969= XM_005244738.1:c.969C>T
TTLL10 transcript variant X1 XM_047416841.1:c.1566= XM_047416841.1:c.1566C>T
TTLL10 transcript variant X4 XM_047416843.1:c.1566= XM_047416843.1:c.1566C>T
TTLL10 transcript variant X3 XM_047416842.1:c.1476= XM_047416842.1:c.1476C>T
TTLL10 transcript variant 3 NM_001371649.1:c.1188= NM_001371649.1:c.1188C>T
TTLL10 transcript variant X9 XM_047416870.1:c.1188= XM_047416870.1:c.1188C>T
TTLL10 transcript variant X11 XM_047416882.1:c.1566= XM_047416882.1:c.1566C>T
inactive polyglycylase TTLL10 isoform X7 XP_016856399.2:p.His522= XP_016856399.2:p.His522=
inactive polyglycylase TTLL10 isoform 2 NP_694986.2:p.His323= NP_694986.2:p.His323=
inactive polyglycylase TTLL10 isoform X2 XP_016856395.2:p.His495= XP_016856395.2:p.His495=
inactive polyglycylase TTLL10 isoform X6 XP_016856398.2:p.His522= XP_016856398.2:p.His522=
inactive polyglycylase TTLL10 isoform X8 XP_016856401.1:p.His396= XP_016856401.1:p.His396=
inactive polyglycylase TTLL10 isoform 1 NP_001123517.1:p.His396= NP_001123517.1:p.His396=
inactive polyglycylase TTLL10 isoform X4 XP_016856396.2:p.His522= XP_016856396.2:p.His522=
inactive polyglycylase TTLL10 isoform X5 XP_016856397.2:p.His522= XP_016856397.2:p.His522=
inactive polyglycylase TTLL10 isoform X10 XP_005244795.1:p.His323= XP_005244795.1:p.His323=
inactive polyglycylase TTLL10 isoform X1 XP_047272797.1:p.His522= XP_047272797.1:p.His522=
inactive polyglycylase TTLL10 isoform X1 XP_047272799.1:p.His522= XP_047272799.1:p.His522=
inactive polyglycylase TTLL10 isoform X3 XP_047272798.1:p.His492= XP_047272798.1:p.His492=
inactive polyglycylase TTLL10 isoform 1 NP_001358578.1:p.His396= NP_001358578.1:p.His396=
inactive polyglycylase TTLL10 isoform X8 XP_047272826.1:p.His396= XP_047272826.1:p.His396=
inactive polyglycylase TTLL10 isoform X9 XP_047272838.1:p.His522= XP_047272838.1:p.His522=
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#.

40 SubSNP, 16 Frequency submissions
No Submitter Submission ID Date (Build)
1 BUSHMAN ss197889672 Jul 04, 2010 (132)
2 1000GENOMES ss217405736 Jul 14, 2010 (132)
3 1000GENOMES ss217410883 Jul 14, 2010 (132)
4 1000GENOMES ss218192288 Jul 14, 2010 (132)
5 NHLBI-ESP ss341924421 May 09, 2011 (134)
6 1000GENOMES ss489714624 May 04, 2012 (137)
7 ILLUMINA ss533943944 Sep 08, 2015 (146)
8 SSMP ss647518899 Apr 25, 2013 (138)
9 JMKIDD_LAB ss1067414447 Aug 21, 2014 (142)
10 JMKIDD_LAB ss1067614025 Aug 21, 2014 (142)
11 1000GENOMES ss1289353118 Aug 21, 2014 (142)
12 EVA_UK10K_ALSPAC ss1599383843 Apr 01, 2015 (144)
13 EVA_UK10K_TWINSUK ss1642377876 Apr 01, 2015 (144)
14 EVA_EXAC ss1685226004 Apr 01, 2015 (144)
15 EVA_MGP ss1710883779 Apr 01, 2015 (144)
16 WEILL_CORNELL_DGM ss1917964767 Feb 12, 2016 (147)
17 ILLUMINA ss1958230923 Feb 12, 2016 (147)
18 HUMAN_LONGEVITY ss2159391844 Dec 20, 2016 (150)
19 GNOMAD ss2731000313 Nov 08, 2017 (151)
20 GNOMAD ss2746174380 Nov 08, 2017 (151)
21 GNOMAD ss2750679605 Nov 08, 2017 (151)
22 ILLUMINA ss3021043878 Nov 08, 2017 (151)
23 ILLUMINA ss3626007216 Oct 11, 2018 (152)
24 ILLUMINA ss3651365932 Oct 11, 2018 (152)
25 ILLUMINA ss3724988536 Jul 12, 2019 (153)
26 PAGE_CC ss3770778895 Jul 12, 2019 (153)
27 EVA ss3823543118 Apr 25, 2020 (154)
28 SGDP_PRJ ss3848005920 Apr 25, 2020 (154)
29 FSA-LAB ss3983910766 Apr 25, 2021 (155)
30 EVA ss3986091327 Apr 25, 2021 (155)
31 TOPMED ss4436540518 Apr 25, 2021 (155)
32 TOMMO_GENOMICS ss5142070238 Apr 25, 2021 (155)
33 1000G_HIGH_COVERAGE ss5240876225 Oct 12, 2022 (156)
34 EVA ss5316203975 Oct 12, 2022 (156)
35 HUGCELL_USP ss5442122487 Oct 12, 2022 (156)
36 1000G_HIGH_COVERAGE ss5512505862 Oct 12, 2022 (156)
37 SANFORD_IMAGENETICS ss5624756898 Oct 12, 2022 (156)
38 TOMMO_GENOMICS ss5666215929 Oct 12, 2022 (156)
39 EVA ss5906717665 Oct 12, 2022 (156)
40 EVA ss5936588961 Oct 12, 2022 (156)
41 1000Genomes NC_000001.10 - 1119399 Oct 11, 2018 (152)
42 1000Genomes_30x NC_000001.11 - 1184019 Oct 12, 2022 (156)
43 The Avon Longitudinal Study of Parents and Children NC_000001.10 - 1119399 Oct 11, 2018 (152)
44 ExAC NC_000001.10 - 1119399 Oct 11, 2018 (152)
45 gnomAD - Genomes NC_000001.11 - 1184019 Apr 25, 2021 (155)
46 gnomAD - Exomes NC_000001.10 - 1119399 Jul 12, 2019 (153)
47 GO Exome Sequencing Project NC_000001.10 - 1119399 Oct 11, 2018 (152)
48 Medical Genome Project healthy controls from Spanish population NC_000001.10 - 1119399 Apr 25, 2020 (154)
49 The PAGE Study NC_000001.11 - 1184019 Jul 12, 2019 (153)
50 Qatari NC_000001.10 - 1119399 Apr 25, 2020 (154)
51 SGDP_PRJ NC_000001.10 - 1119399 Apr 25, 2020 (154)
52 8.3KJPN NC_000001.10 - 1119399 Apr 25, 2021 (155)
53 14KJPN NC_000001.11 - 1184019 Oct 12, 2022 (156)
54 TopMed NC_000001.11 - 1184019 Apr 25, 2021 (155)
55 UK 10K study - Twins NC_000001.10 - 1119399 Oct 11, 2018 (152)
56 ALFA NC_000001.11 - 1184019 Apr 25, 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
ss197889672, ss217405736, ss217410883 NC_000001.9:1109261:C:T NC_000001.11:1184018:C:T (self)
18304, 6287, 4399687, 15157, 1855, 531, 6697, 22900, 39545, 6287, ss218192288, ss341924421, ss489714624, ss533943944, ss647518899, ss1067414447, ss1067614025, ss1289353118, ss1599383843, ss1642377876, ss1685226004, ss1710883779, ss1917964767, ss1958230923, ss2731000313, ss2746174380, ss2750679605, ss3021043878, ss3626007216, ss3651365932, ss3823543118, ss3848005920, ss3983910766, ss3986091327, ss5142070238, ss5316203975, ss5624756898, ss5936588961 NC_000001.10:1119398:C:T NC_000001.11:1184018:C:T (self)
31797, 159812, 364, 53033, 146853, 3005699458, ss2159391844, ss3724988536, ss3770778895, ss4436540518, ss5240876225, ss5442122487, ss5512505862, ss5666215929, ss5906717665 NC_000001.11:1184018:C:T NC_000001.11:1184018:C:T (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 rs112690643

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.post761+d5e8e07