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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.

rs111751804

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr1:1180123 (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
T>C
Variation Type
SNV Single Nucleotide Variation
Frequency
C=0.013835 (3662/264690, TOPMED)
C=0.019366 (4631/239128, GnomAD_exome)
C=0.019098 (2676/140122, GnomAD) (+ 17 more)
C=0.025683 (3423/133278, ALFA)
C=0.02245 (2189/97498, ExAC)
C=0.00526 (414/78646, PAGE_STUDY)
C=0.00006 (1/16760, 8.3KJPN)
C=0.01809 (235/12992, GO-ESP)
C=0.0106 (53/5008, 1000G)
C=0.0730 (327/4480, Estonian)
C=0.0226 (87/3854, ALSPAC)
C=0.0186 (69/3708, TWINSUK)
C=0.033 (20/600, NorthernSweden)
C=0.023 (6/264, FINRISK)
C=0.009 (2/216, Qatari)
C=0.05 (2/40, GENOME_DK)
T=0.5 (5/10, SGDP_PRJ)
C=0.5 (5/10, SGDP_PRJ)
T=0.5 (1/2, Siberian)
C=0.5 (1/2, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
TTLL10 : Missense Variant
TTLL10-AS1 : 2KB Upstream 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 1 NC_000001.11:g.1180123T>C
GRCh37.p13 chr 1 NC_000001.10:g.1115503T>C
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.70T>C C [TGT] > R [CGT] Coding Sequence Variant
inactive polyglycylase TTLL10 isoform 2 NP_694986.2:p.Cys24Arg C (Cys) > R (Arg) Missense Variant
TTLL10 transcript variant 1 NM_001130045.2:c.289T>C C [TGT] > R [CGT] Coding Sequence Variant
inactive polyglycylase TTLL10 isoform 1 NP_001123517.1:p.Cys97Arg C (Cys) > R (Arg) Missense Variant
TTLL10 transcript variant 3 NM_001371649.1:c.289T>C C [TGT] > R [CGT] Coding Sequence Variant
inactive polyglycylase TTLL10 isoform 1 NP_001358578.1:p.Cys97Arg C (Cys) > R (Arg) Missense Variant
TTLL10 transcript variant X10 XM_005244738.1:c.70T>C C [TGT] > R [CGT] Coding Sequence Variant
inactive polyglycylase TTLL10 isoform X8 XP_005244795.1:p.Cys24Arg C (Cys) > R (Arg) Missense Variant
TTLL10 transcript variant X1 XM_017000906.1:c.208T>C C [TGT] > R [CGT] Coding Sequence Variant
inactive polyglycylase TTLL10 isoform X1 XP_016856395.1:p.Cys70Arg C (Cys) > R (Arg) Missense Variant
TTLL10 transcript variant X2 XM_017000907.1:c.289T>C C [TGT] > R [CGT] Coding Sequence Variant
inactive polyglycylase TTLL10 isoform X2 XP_016856396.1:p.Cys97Arg C (Cys) > R (Arg) Missense Variant
TTLL10 transcript variant X3 XM_017000908.1:c.289T>C C [TGT] > R [CGT] Coding Sequence Variant
inactive polyglycylase TTLL10 isoform X3 XP_016856397.1:p.Cys97Arg C (Cys) > R (Arg) Missense Variant
TTLL10 transcript variant X4 XM_017000909.1:c.289T>C C [TGT] > R [CGT] Coding Sequence Variant
inactive polyglycylase TTLL10 isoform X4 XP_016856398.1:p.Cys97Arg C (Cys) > R (Arg) Missense Variant
TTLL10 transcript variant X6 XM_017000911.1:c.289T>C C [TGT] > R [CGT] Coding Sequence Variant
inactive polyglycylase TTLL10 isoform X6 XP_016856400.1:p.Cys97Arg C (Cys) > R (Arg) Missense Variant
TTLL10 transcript variant X7 XM_011541177.2:c.289T>C C [TGT] > R [CGT] Coding Sequence Variant
inactive polyglycylase TTLL10 isoform X7 XP_011539479.1:p.Cys97Arg C (Cys) > R (Arg) Missense Variant
TTLL10 transcript variant X8 XM_017000912.1:c.289T>C C [TGT] > R [CGT] Coding Sequence Variant
inactive polyglycylase TTLL10 isoform X7 XP_016856401.1:p.Cys97Arg C (Cys) > R (Arg) Missense Variant
TTLL10 transcript variant X5 XM_017000910.2:c.289T>C C [TGT] > R [CGT] Coding Sequence Variant
inactive polyglycylase TTLL10 isoform X5 XP_016856399.1:p.Cys97Arg C (Cys) > R (Arg) Missense Variant
TTLL10 transcript variant X9 XR_001737088.1:n.599T>C N/A Non Coding Transcript Variant
TTLL10 transcript variant X11 XR_001737089.1:n.989T>C N/A Non Coding Transcript Variant
Gene: TTLL10-AS1, uncharacterized TTLL10-AS1 (minus strand) : 2KB Upstream Variant
Molecule type Change Amino acid[Codon] SO Term
TTLL10-AS1 transcript variant X2 XR_132470.6:n. N/A Upstream Transcript Variant
TTLL10-AS1 transcript variant X1 XR_946813.2:n. N/A Upstream Transcript 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 133278 T=0.974317 C=0.025683
European Sub 114284 T=0.972910 C=0.027090
African Sub 4176 T=0.9947 C=0.0053
African Others Sub 124 T=1.000 C=0.000
African American Sub 4052 T=0.9946 C=0.0054
Asian Sub 236 T=1.000 C=0.000
East Asian Sub 152 T=1.000 C=0.000
Other Asian Sub 84 T=1.00 C=0.00
Latin American 1 Sub 514 T=0.994 C=0.006
Latin American 2 Sub 656 T=0.991 C=0.009
South Asian Sub 104 T=0.990 C=0.010
Other Sub 13308 T=0.97783 C=0.02217


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 T=0.986165 C=0.013835
gnomAD - Exomes Global Study-wide 239128 T=0.980634 C=0.019366
gnomAD - Exomes European Sub 126214 T=0.970059 C=0.029941
gnomAD - Exomes Asian Sub 48188 T=0.99278 C=0.00722
gnomAD - Exomes American Sub 34062 T=0.99513 C=0.00487
gnomAD - Exomes African Sub 15184 T=0.99737 C=0.00263
gnomAD - Exomes Ashkenazi Jewish Sub 9654 T=0.9793 C=0.0207
gnomAD - Exomes Other Sub 5826 T=0.9832 C=0.0168
gnomAD - Genomes Global Study-wide 140122 T=0.980902 C=0.019098
gnomAD - Genomes European Sub 75884 T=0.96978 C=0.03022
gnomAD - Genomes African Sub 41986 T=0.99636 C=0.00364
gnomAD - Genomes American Sub 13650 T=0.99026 C=0.00974
gnomAD - Genomes Ashkenazi Jewish Sub 3316 T=0.9822 C=0.0178
gnomAD - Genomes East Asian Sub 3134 T=1.0000 C=0.0000
gnomAD - Genomes Other Sub 2152 T=0.9823 C=0.0177
ExAC Global Study-wide 97498 T=0.97755 C=0.02245
ExAC Europe Sub 58806 T=0.96720 C=0.03280
ExAC Asian Sub 21130 T=0.99219 C=0.00781
ExAC American Sub 9170 T=0.9949 C=0.0051
ExAC African Sub 7722 T=0.9961 C=0.0039
ExAC Other Sub 670 T=0.973 C=0.027
The PAGE Study Global Study-wide 78646 T=0.99474 C=0.00526
The PAGE Study AfricanAmerican Sub 32482 T=0.99584 C=0.00416
The PAGE Study Mexican Sub 10808 T=0.99352 C=0.00648
The PAGE Study Asian Sub 8310 T=0.9989 C=0.0011
The PAGE Study PuertoRican Sub 7916 T=0.9937 C=0.0063
The PAGE Study NativeHawaiian Sub 4530 T=0.9958 C=0.0042
The PAGE Study Cuban Sub 4228 T=0.9901 C=0.0099
The PAGE Study Dominican Sub 3828 T=0.9953 C=0.0047
The PAGE Study CentralAmerican Sub 2448 T=0.9943 C=0.0057
The PAGE Study SouthAmerican Sub 1982 T=0.9934 C=0.0066
The PAGE Study NativeAmerican Sub 1260 T=0.9802 C=0.0198
The PAGE Study SouthAsian Sub 854 T=0.978 C=0.022
8.3KJPN JAPANESE Study-wide 16760 T=0.99994 C=0.00006
GO Exome Sequencing Project Global Study-wide 12992 T=0.98191 C=0.01809
GO Exome Sequencing Project European American Sub 8592 T=0.9747 C=0.0253
GO Exome Sequencing Project African American Sub 4400 T=0.9959 C=0.0041
1000Genomes Global Study-wide 5008 T=0.9894 C=0.0106
1000Genomes African Sub 1322 T=0.9962 C=0.0038
1000Genomes East Asian Sub 1008 T=1.0000 C=0.0000
1000Genomes Europe Sub 1006 T=0.9692 C=0.0308
1000Genomes South Asian Sub 978 T=0.988 C=0.012
1000Genomes American Sub 694 T=0.993 C=0.007
Genetic variation in the Estonian population Estonian Study-wide 4480 T=0.9270 C=0.0730
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.9774 C=0.0226
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.9814 C=0.0186
Northern Sweden ACPOP Study-wide 600 T=0.967 C=0.033
FINRISK Finnish from FINRISK project Study-wide 264 T=0.977 C=0.023
Qatari Global Study-wide 216 T=0.991 C=0.009
The Danish reference pan genome Danish Study-wide 40 T=0.95 C=0.05
SGDP_PRJ Global Study-wide 10 T=0.5 C=0.5
Siberian Global Study-wide 2 T=0.5 C=0.5
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 T= C
GRCh38.p13 chr 1 NC_000001.11:g.1180123= NC_000001.11:g.1180123T>C
GRCh37.p13 chr 1 NC_000001.10:g.1115503= NC_000001.10:g.1115503T>C
TTLL10 transcript variant 2 NM_153254.3:c.70= NM_153254.3:c.70T>C
TTLL10 transcript variant 2 NM_153254.2:c.70= NM_153254.2:c.70T>C
TTLL10 transcript variant X7 XM_011541177.2:c.289= XM_011541177.2:c.289T>C
TTLL10 transcript variant 1 NM_001130045.2:c.289= NM_001130045.2:c.289T>C
TTLL10 transcript variant 1 NM_001130045.1:c.289= NM_001130045.1:c.289T>C
TTLL10 transcript variant X5 XM_017000910.2:c.289= XM_017000910.2:c.289T>C
TTLL10 transcript variant X1 XM_017000906.1:c.208= XM_017000906.1:c.208T>C
TTLL10 transcript variant 3 NM_001371649.1:c.289= NM_001371649.1:c.289T>C
TTLL10 transcript variant X8 XM_017000912.1:c.289= XM_017000912.1:c.289T>C
TTLL10 transcript variant X4 XM_017000909.1:c.289= XM_017000909.1:c.289T>C
TTLL10 transcript variant X10 XM_005244738.1:c.70= XM_005244738.1:c.70T>C
TTLL10 transcript variant X9 XR_001737088.1:n.599= XR_001737088.1:n.599T>C
TTLL10 transcript variant X3 XM_017000908.1:c.289= XM_017000908.1:c.289T>C
TTLL10 transcript variant X2 XM_017000907.1:c.289= XM_017000907.1:c.289T>C
TTLL10 transcript variant X6 XM_017000911.1:c.289= XM_017000911.1:c.289T>C
TTLL10 transcript variant X11 XR_001737089.1:n.989= XR_001737089.1:n.989T>C
inactive polyglycylase TTLL10 isoform 2 NP_694986.2:p.Cys24= NP_694986.2:p.Cys24Arg
inactive polyglycylase TTLL10 isoform X7 XP_011539479.1:p.Cys97= XP_011539479.1:p.Cys97Arg
inactive polyglycylase TTLL10 isoform 1 NP_001123517.1:p.Cys97= NP_001123517.1:p.Cys97Arg
inactive polyglycylase TTLL10 isoform X5 XP_016856399.1:p.Cys97= XP_016856399.1:p.Cys97Arg
inactive polyglycylase TTLL10 isoform X1 XP_016856395.1:p.Cys70= XP_016856395.1:p.Cys70Arg
inactive polyglycylase TTLL10 isoform 1 NP_001358578.1:p.Cys97= NP_001358578.1:p.Cys97Arg
inactive polyglycylase TTLL10 isoform X7 XP_016856401.1:p.Cys97= XP_016856401.1:p.Cys97Arg
inactive polyglycylase TTLL10 isoform X4 XP_016856398.1:p.Cys97= XP_016856398.1:p.Cys97Arg
inactive polyglycylase TTLL10 isoform X8 XP_005244795.1:p.Cys24= XP_005244795.1:p.Cys24Arg
inactive polyglycylase TTLL10 isoform X3 XP_016856397.1:p.Cys97= XP_016856397.1:p.Cys97Arg
inactive polyglycylase TTLL10 isoform X2 XP_016856396.1:p.Cys97= XP_016856396.1:p.Cys97Arg
inactive polyglycylase TTLL10 isoform X6 XP_016856400.1:p.Cys97= XP_016856400.1:p.Cys97Arg
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#.

60 SubSNP, 18 Frequency submissions
No Submitter Submission ID Date (Build)
1 COMPLETE_GENOMICS ss163708553 Jul 04, 2010 (132)
2 1000GENOMES ss217314356 Jul 14, 2010 (132)
3 1000GENOMES ss217410436 Jul 14, 2010 (132)
4 1000GENOMES ss230396629 Jul 14, 2010 (132)
5 NHLBI-ESP ss341924370 May 09, 2011 (134)
6 1000GENOMES ss489714583 May 04, 2012 (137)
7 EXOME_CHIP ss491284053 May 04, 2012 (137)
8 CLINSEQ_SNP ss491581868 May 04, 2012 (137)
9 ILLUMINA ss535698261 Sep 08, 2015 (146)
10 ILLUMINA ss780756265 Aug 21, 2014 (142)
11 ILLUMINA ss783434679 Aug 21, 2014 (142)
12 EVA-GONL ss974772644 Aug 21, 2014 (142)
13 1000GENOMES ss1289352907 Aug 21, 2014 (142)
14 EVA_GENOME_DK ss1573852234 Apr 01, 2015 (144)
15 EVA_FINRISK ss1584003644 Apr 01, 2015 (144)
16 EVA_DECODE ss1584132568 Apr 01, 2015 (144)
17 EVA_UK10K_ALSPAC ss1599383771 Apr 01, 2015 (144)
18 EVA_UK10K_TWINSUK ss1642377804 Apr 01, 2015 (144)
19 EVA_EXAC ss1685225656 Apr 01, 2015 (144)
20 ILLUMINA ss1751863268 Sep 08, 2015 (146)
21 ILLUMINA ss1917720985 Feb 12, 2016 (147)
22 WEILL_CORNELL_DGM ss1917964719 Feb 12, 2016 (147)
23 ILLUMINA ss1945981820 Feb 12, 2016 (147)
24 ILLUMINA ss1958230892 Feb 12, 2016 (147)
25 JJLAB ss2019500187 Sep 14, 2016 (149)
26 USC_VALOUEV ss2147487056 Dec 20, 2016 (150)
27 HUMAN_LONGEVITY ss2159391487 Dec 20, 2016 (150)
28 TOPMED ss2321530705 Dec 20, 2016 (150)
29 GNOMAD ss2730999788 Nov 08, 2017 (151)
30 GNOMAD ss2746174188 Nov 08, 2017 (151)
31 GNOMAD ss2750679124 Nov 08, 2017 (151)
32 AFFY ss2984841267 Nov 08, 2017 (151)
33 SWEGEN ss2986155451 Nov 08, 2017 (151)
34 ILLUMINA ss3021043846 Nov 08, 2017 (151)
35 TOPMED ss3066487766 Nov 08, 2017 (151)
36 ILLUMINA ss3626007195 Oct 11, 2018 (152)
37 ILLUMINA ss3626007196 Oct 11, 2018 (152)
38 ILLUMINA ss3634302090 Oct 11, 2018 (152)
39 ILLUMINA ss3640009456 Oct 11, 2018 (152)
40 ILLUMINA ss3644477684 Oct 11, 2018 (152)
41 ILLUMINA ss3651365899 Oct 11, 2018 (152)
42 ILLUMINA ss3653615033 Oct 11, 2018 (152)
43 EGCUT_WGS ss3654266494 Jul 12, 2019 (153)
44 EVA_DECODE ss3685999324 Jul 12, 2019 (153)
45 ILLUMINA ss3724988515 Jul 12, 2019 (153)
46 ACPOP ss3726719296 Jul 12, 2019 (153)
47 ILLUMINA ss3744337413 Jul 12, 2019 (153)
48 ILLUMINA ss3744603021 Jul 12, 2019 (153)
49 EVA ss3745725067 Jul 12, 2019 (153)
50 PAGE_CC ss3770778879 Jul 12, 2019 (153)
51 ILLUMINA ss3772104779 Jul 12, 2019 (153)
52 KHV_HUMAN_GENOMES ss3798747717 Jul 12, 2019 (153)
53 EVA ss3823543020 Apr 25, 2020 (154)
54 EVA ss3825549311 Apr 25, 2020 (154)
55 SGDP_PRJ ss3848005816 Apr 25, 2020 (154)
56 EVA ss3986091282 Apr 25, 2021 (155)
57 TOPMED ss4436539226 Apr 25, 2021 (155)
58 TOMMO_GENOMICS ss5142070036 Apr 25, 2021 (155)
59 EVA ss5236862459 Apr 25, 2021 (155)
60 EVA ss5237258295 Apr 25, 2021 (155)
61 1000Genomes NC_000001.10 - 1115503 Oct 11, 2018 (152)
62 The Avon Longitudinal Study of Parents and Children NC_000001.10 - 1115503 Oct 11, 2018 (152)
63 Genetic variation in the Estonian population NC_000001.10 - 1115503 Oct 11, 2018 (152)
64 ExAC NC_000001.10 - 1115503 Oct 11, 2018 (152)
65 FINRISK NC_000001.10 - 1115503 Apr 25, 2020 (154)
66 The Danish reference pan genome NC_000001.10 - 1115503 Apr 25, 2020 (154)
67 gnomAD - Genomes NC_000001.11 - 1180123 Apr 25, 2021 (155)
68 gnomAD - Exomes NC_000001.10 - 1115503 Jul 12, 2019 (153)
69 GO Exome Sequencing Project NC_000001.10 - 1115503 Oct 11, 2018 (152)
70 Northern Sweden NC_000001.10 - 1115503 Jul 12, 2019 (153)
71 The PAGE Study NC_000001.11 - 1180123 Jul 12, 2019 (153)
72 Qatari NC_000001.10 - 1115503 Apr 25, 2020 (154)
73 SGDP_PRJ NC_000001.10 - 1115503 Apr 25, 2020 (154)
74 Siberian NC_000001.10 - 1115503 Apr 25, 2020 (154)
75 8.3KJPN NC_000001.10 - 1115503 Apr 25, 2021 (155)
76 TopMed NC_000001.11 - 1180123 Apr 25, 2021 (155)
77 UK 10K study - Twins NC_000001.10 - 1115503 Oct 11, 2018 (152)
78 ALFA NC_000001.11 - 1180123 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
ss163708553, ss217314356, ss217410436, ss491581868, ss1584132568 NC_000001.9:1105365:T:C NC_000001.11:1180122:T:C (self)
18091, 6213, 4742, 4399306, 105, 1359468, 14612, 1757, 4161, 6649, 22796, 3410, 39343, 6213, ss230396629, ss341924370, ss489714583, ss491284053, ss535698261, ss780756265, ss783434679, ss974772644, ss1289352907, ss1573852234, ss1584003644, ss1599383771, ss1642377804, ss1685225656, ss1751863268, ss1917720985, ss1917964719, ss1945981820, ss1958230892, ss2019500187, ss2147487056, ss2321530705, ss2730999788, ss2746174188, ss2750679124, ss2984841267, ss2986155451, ss3021043846, ss3626007195, ss3626007196, ss3634302090, ss3640009456, ss3644477684, ss3651365899, ss3653615033, ss3654266494, ss3726719296, ss3744337413, ss3744603021, ss3745725067, ss3772104779, ss3823543020, ss3825549311, ss3848005816, ss3986091282, ss5142070036, ss5237258295 NC_000001.10:1115502:T:C NC_000001.11:1180122:T:C (self)
158732, 348, 83516, 145561, 14266885805, ss2159391487, ss3066487766, ss3685999324, ss3724988515, ss3770778879, ss3798747717, ss4436539226, ss5236862459 NC_000001.11:1180122:T:C NC_000001.11:1180122:T:C (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 rs111751804

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