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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.

rs79434849

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr21:44439159 (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>G / C>T
Variation Type
SNV Single Nucleotide Variation
Frequency
T=0.001862 (467/250820, GnomAD_exome)
T=0.002615 (314/120098, ExAC)
T=0.00157 (93/59114, ALFA) (+ 7 more)
T=0.00004 (1/28258, 14KJPN)
T=0.00006 (1/16760, 8.3KJPN)
T=0.00900 (117/13006, GO-ESP)
T=0.0101 (65/6404, 1000G_30x)
T=0.0098 (49/5008, 1000G)
G=0.0007 (2/2922, KOREAN)
C=0.38 (6/16, SGDP_PRJ)
Clinical Significance
Reported in ClinVar
Gene : Consequence
TRPM2 : Missense Variant
LOC124905068 : 500B Downstream 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 75472 C=0.99693 G=0.00000, T=0.00307
European Sub 53338 C=0.99994 G=0.00000, T=0.00006
African Sub 11502 C=0.98200 G=0.00000, T=0.01800
African Others Sub 392 C=0.972 G=0.000, T=0.028
African American Sub 11110 C=0.98236 G=0.00000, T=0.01764
Asian Sub 184 C=1.000 G=0.000, T=0.000
East Asian Sub 126 C=1.000 G=0.000, T=0.000
Other Asian Sub 58 C=1.00 G=0.00, T=0.00
Latin American 1 Sub 516 C=0.990 G=0.000, T=0.010
Latin American 2 Sub 716 C=1.000 G=0.000, T=0.000
South Asian Sub 114 C=1.000 G=0.000, T=0.000
Other Sub 9102 C=0.9981 G=0.0000, T=0.0019


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
gnomAD - Exomes Global Study-wide 250820 C=0.998138 T=0.001862
gnomAD - Exomes European Sub 134908 C=0.999956 T=0.000044
gnomAD - Exomes Asian Sub 48994 C=0.99998 T=0.00002
gnomAD - Exomes American Sub 34542 C=0.99925 T=0.00075
gnomAD - Exomes African Sub 16202 C=0.97346 T=0.02654
gnomAD - Exomes Ashkenazi Jewish Sub 10050 C=1.00000 T=0.00000
gnomAD - Exomes Other Sub 6124 C=0.9993 T=0.0007
ExAC Global Study-wide 120098 C=0.997385 T=0.002615
ExAC Europe Sub 72416 C=0.99997 T=0.00003
ExAC Asian Sub 25078 C=0.99996 T=0.00004
ExAC American Sub 11496 C=0.99913 T=0.00087
ExAC African Sub 10216 C=0.97073 T=0.02927
ExAC Other Sub 892 C=0.998 T=0.002
Allele Frequency Aggregator Total Global 59114 C=0.99843 G=0.00000, T=0.00157
Allele Frequency Aggregator European Sub 43248 C=0.99995 G=0.00000, T=0.00005
Allele Frequency Aggregator Other Sub 7668 C=0.9987 G=0.0000, T=0.0013
Allele Frequency Aggregator African Sub 6668 C=0.9886 G=0.0000, T=0.0114
Allele Frequency Aggregator Latin American 2 Sub 716 C=1.000 G=0.000, T=0.000
Allele Frequency Aggregator Latin American 1 Sub 516 C=0.990 G=0.000, T=0.010
Allele Frequency Aggregator Asian Sub 184 C=1.000 G=0.000, T=0.000
Allele Frequency Aggregator South Asian Sub 114 C=1.000 G=0.000, T=0.000
14KJPN JAPANESE Study-wide 28258 C=0.99996 T=0.00004
8.3KJPN JAPANESE Study-wide 16760 C=0.99994 T=0.00006
GO Exome Sequencing Project Global Study-wide 13006 C=0.99100 T=0.00900
GO Exome Sequencing Project European American Sub 8600 C=1.0000 T=0.0000
GO Exome Sequencing Project African American Sub 4406 C=0.9734 T=0.0266
1000Genomes_30x Global Study-wide 6404 C=0.9899 T=0.0101
1000Genomes_30x African Sub 1786 C=0.9670 T=0.0330
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=0.994 T=0.006
1000Genomes Global Study-wide 5008 C=0.9902 T=0.0098
1000Genomes African Sub 1322 C=0.9652 T=0.0348
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=0.996 T=0.004
KOREAN population from KRGDB KOREAN Study-wide 2922 C=0.9993 G=0.0007
SGDP_PRJ Global Study-wide 16 C=0.38 T=0.62
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 21 NC_000021.9:g.44439159C>G
GRCh38.p14 chr 21 NC_000021.9:g.44439159C>T
GRCh37.p13 chr 21 NC_000021.8:g.45859042C>G
GRCh37.p13 chr 21 NC_000021.8:g.45859042C>T
TRPM2 RefSeqGene NG_022913.1:g.90559C>G
TRPM2 RefSeqGene NG_022913.1:g.90559C>T
Gene: TRPM2, transient receptor potential cation channel subfamily M member 2 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
TRPM2 transcript variant 5 NM_001320352.3:c.303C>G C [TGC] > W [TGG] Coding Sequence Variant
transient receptor potential cation channel subfamily M member 2 isoform 4 NP_001307281.1:p.Cys101Trp C (Cys) > W (Trp) Missense Variant
TRPM2 transcript variant 5 NM_001320352.3:c.303C>T C [TGC] > C [TGT] Coding Sequence Variant
transient receptor potential cation channel subfamily M member 2 isoform 4 NP_001307281.1:p.Cys101= C (Cys) > C (Cys) Synonymous Variant
TRPM2 transcript variant 4 NM_001320351.2:c.4158C>G C [TGC] > W [TGG] Coding Sequence Variant
transient receptor potential cation channel subfamily M member 2 isoform 3 NP_001307280.2:p.Cys1386T…

NP_001307280.2:p.Cys1386Trp

 		C (Cys) > W (Trp) Missense Variant
TRPM2 transcript variant 4 NM_001320351.2:c.4158C>T C [TGC] > C [TGT] Coding Sequence Variant
transient receptor potential cation channel subfamily M member 2 isoform 3 NP_001307280.2:p.Cys1386= C (Cys) > C (Cys) Synonymous Variant
TRPM2 transcript variant 3 NM_001320350.2:c.4410C>G C [TGC] > W [TGG] Coding Sequence Variant
transient receptor potential cation channel subfamily M member 2 isoform 2 NP_001307279.2:p.Cys1470T…

NP_001307279.2:p.Cys1470Trp

 		C (Cys) > W (Trp) Missense Variant
TRPM2 transcript variant 3 NM_001320350.2:c.4410C>T C [TGC] > C [TGT] Coding Sequence Variant
transient receptor potential cation channel subfamily M member 2 isoform 2 NP_001307279.2:p.Cys1470= C (Cys) > C (Cys) Synonymous Variant
TRPM2 transcript variant 1 NM_003307.4:c.4260C>G C [TGC] > W [TGG] Coding Sequence Variant
transient receptor potential cation channel subfamily M member 2 isoform 1 NP_003298.2:p.Cys1420Trp C (Cys) > W (Trp) Missense Variant
TRPM2 transcript variant 1 NM_003307.4:c.4260C>T C [TGC] > C [TGT] Coding Sequence Variant
transient receptor potential cation channel subfamily M member 2 isoform 1 NP_003298.2:p.Cys1420= C (Cys) > C (Cys) Synonymous Variant
TRPM2 transcript variant 2 NR_038257.2:n.4343C>G N/A Non Coding Transcript Variant
TRPM2 transcript variant 2 NR_038257.2:n.4343C>T N/A Non Coding Transcript Variant
TRPM2 transcript variant X3 XM_047440977.1:c. N/A Genic Downstream Transcript Variant
TRPM2 transcript variant X4 XM_047440978.1:c. N/A Genic Downstream Transcript Variant
TRPM2 transcript variant X5 XM_047440979.1:c. N/A Genic Downstream Transcript Variant
TRPM2 transcript variant X1 XM_011529736.3:c.4350C>G C [TGC] > W [TGG] Coding Sequence Variant
transient receptor potential cation channel subfamily M member 2 isoform X1 XP_011528038.1:p.Cys1450T…

XP_011528038.1:p.Cys1450Trp

 		C (Cys) > W (Trp) Missense Variant
TRPM2 transcript variant X1 XM_011529736.3:c.4350C>T C [TGC] > C [TGT] Coding Sequence Variant
transient receptor potential cation channel subfamily M member 2 isoform X1 XP_011528038.1:p.Cys1450= C (Cys) > C (Cys) Synonymous Variant
TRPM2 transcript variant X2 XM_017028457.3:c.4248C>G C [TGC] > W [TGG] Coding Sequence Variant
transient receptor potential cation channel subfamily M member 2 isoform X2 XP_016883946.1:p.Cys1416T…

XP_016883946.1:p.Cys1416Trp

 		C (Cys) > W (Trp) Missense Variant
TRPM2 transcript variant X2 XM_017028457.3:c.4248C>T C [TGC] > C [TGT] Coding Sequence Variant
transient receptor potential cation channel subfamily M member 2 isoform X2 XP_016883946.1:p.Cys1416= C (Cys) > C (Cys) Synonymous Variant
Gene: LOC124905068, uncharacterized LOC124905068 (plus strand) : 500B Downstream Variant
Molecule type Change Amino acid[Codon] SO Term
LOC124905068 transcript XR_007067943.1:n. N/A Downstream 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.

Allele: T (allele ID: 717253 )
ClinVar Accession Disease Names Clinical Significance
RCV000967576.3 not provided 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 C= G T
GRCh38.p14 chr 21 NC_000021.9:g.44439159= NC_000021.9:g.44439159C>G NC_000021.9:g.44439159C>T
GRCh37.p13 chr 21 NC_000021.8:g.45859042= NC_000021.8:g.45859042C>G NC_000021.8:g.45859042C>T
TRPM2 RefSeqGene NG_022913.1:g.90559= NG_022913.1:g.90559C>G NG_022913.1:g.90559C>T
TRPM2 transcript variant 1 NM_003307.4:c.4260= NM_003307.4:c.4260C>G NM_003307.4:c.4260C>T
TRPM2 transcript variant 1 NM_003307.3:c.4260= NM_003307.3:c.4260C>G NM_003307.3:c.4260C>T
TRPM2 transcript variant 5 NM_001320352.3:c.303= NM_001320352.3:c.303C>G NM_001320352.3:c.303C>T
TRPM2 transcript variant 5 NM_001320352.2:c.303= NM_001320352.2:c.303C>G NM_001320352.2:c.303C>T
TRPM2 transcript variant 5 NM_001320352.1:c.303= NM_001320352.1:c.303C>G NM_001320352.1:c.303C>T
TRPM2 transcript variant 3 NM_001320350.2:c.4410= NM_001320350.2:c.4410C>G NM_001320350.2:c.4410C>T
TRPM2 transcript variant 3 NM_001320350.1:c.4410= NM_001320350.1:c.4410C>G NM_001320350.1:c.4410C>T
TRPM2 transcript variant 2 NR_038257.2:n.4343= NR_038257.2:n.4343C>G NR_038257.2:n.4343C>T
TRPM2 transcript variant 2 NR_038257.1:n.4363= NR_038257.1:n.4363C>G NR_038257.1:n.4363C>T
TRPM2 transcript variant 4 NM_001320351.2:c.4158= NM_001320351.2:c.4158C>G NM_001320351.2:c.4158C>T
TRPM2 transcript variant 4 NM_001320351.1:c.4158= NM_001320351.1:c.4158C>G NM_001320351.1:c.4158C>T
TRPM2 transcript variant S NM_001001188.3:c.*1722= NM_001001188.3:c.*1722C>G NM_001001188.3:c.*1722C>T
TRPM2 transcript variant X1 XM_011529736.3:c.4350= XM_011529736.3:c.4350C>G XM_011529736.3:c.4350C>T
TRPM2 transcript variant X1 XM_011529736.2:c.4350= XM_011529736.2:c.4350C>G XM_011529736.2:c.4350C>T
TRPM2 transcript variant X3 XM_011529736.1:c.4350= XM_011529736.1:c.4350C>G XM_011529736.1:c.4350C>T
TRPM2 transcript variant X2 XM_017028457.3:c.4248= XM_017028457.3:c.4248C>G XM_017028457.3:c.4248C>T
TRPM2 transcript variant X4 XM_017028457.2:c.4248= XM_017028457.2:c.4248C>G XM_017028457.2:c.4248C>T
TRPM2 transcript variant X4 XM_017028457.1:c.4248= XM_017028457.1:c.4248C>G XM_017028457.1:c.4248C>T
TRPM2 transcript variant S NM_001001188.2:c.*1722= NM_001001188.2:c.*1722C>G NM_001001188.2:c.*1722C>T
transient receptor potential cation channel subfamily M member 2 isoform 1 NP_003298.2:p.Cys1420= NP_003298.2:p.Cys1420Trp NP_003298.2:p.Cys1420=
transient receptor potential cation channel subfamily M member 2 isoform 4 NP_001307281.1:p.Cys101= NP_001307281.1:p.Cys101Trp NP_001307281.1:p.Cys101=
transient receptor potential cation channel subfamily M member 2 isoform 2 NP_001307279.2:p.Cys1470= NP_001307279.2:p.Cys1470Trp NP_001307279.2:p.Cys1470=
transient receptor potential cation channel subfamily M member 2 isoform 3 NP_001307280.2:p.Cys1386= NP_001307280.2:p.Cys1386Trp NP_001307280.2:p.Cys1386=
transient receptor potential cation channel subfamily M member 2 isoform X1 XP_011528038.1:p.Cys1450= XP_011528038.1:p.Cys1450Trp XP_011528038.1:p.Cys1450=
transient receptor potential cation channel subfamily M member 2 isoform X2 XP_016883946.1:p.Cys1416= XP_016883946.1:p.Cys1416Trp XP_016883946.1:p.Cys1416=
transient receptor potential cation channel subfamily M member 2 isoform 1 NP_003298.1:p.Cys1420= NP_003298.1:p.Cys1420Trp NP_003298.1:p.Cys1420=
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#.

41 SubSNP, 14 Frequency, 1 ClinVar submissions
No Submitter Submission ID Date (Build)
1 BUSHMAN ss204035302 Jul 04, 2010 (132)
2 1000GENOMES ss228595636 Jul 14, 2010 (132)
3 NHLBI-ESP ss342534385 May 09, 2011 (134)
4 ILLUMINA ss480256520 May 04, 2012 (137)
5 ILLUMINA ss484280859 May 04, 2012 (137)
6 1000GENOMES ss491186345 May 04, 2012 (137)
7 ILLUMINA ss533636126 Sep 08, 2015 (146)
8 ILLUMINA ss779187203 Sep 08, 2015 (146)
9 ILLUMINA ss781185896 Sep 08, 2015 (146)
10 ILLUMINA ss834652657 Sep 08, 2015 (146)
11 JMKIDD_LAB ss974511614 Aug 21, 2014 (142)
12 JMKIDD_LAB ss1067602636 Aug 21, 2014 (142)
13 JMKIDD_LAB ss1082541681 Aug 21, 2014 (142)
14 1000GENOMES ss1366501125 Aug 21, 2014 (142)
15 EVA_EXAC ss1694183399 Apr 01, 2015 (144)
16 HUMAN_LONGEVITY ss2246176171 Dec 20, 2016 (150)
17 ILLUMINA ss2633857103 Nov 08, 2017 (151)
18 GRF ss2704475166 Nov 08, 2017 (151)
19 GNOMAD ss2750474437 Nov 08, 2017 (151)
20 GNOMAD ss2972379565 Nov 08, 2017 (151)
21 ILLUMINA ss3022165665 Nov 08, 2017 (151)
22 ILLUMINA ss3628495540 Oct 12, 2018 (152)
23 ILLUMINA ss3631810095 Oct 12, 2018 (152)
24 ILLUMINA ss3652626895 Oct 12, 2018 (152)
25 ILLUMINA ss3725952920 Jul 13, 2019 (153)
26 KHV_HUMAN_GENOMES ss3822340433 Jul 13, 2019 (153)
27 EVA ss3825413667 Apr 27, 2020 (154)
28 SGDP_PRJ ss3890122581 Apr 27, 2020 (154)
29 KRGDB ss3940472995 Apr 27, 2020 (154)
30 EVA ss3986848935 Apr 27, 2021 (155)
31 TOPMED ss5103257326 Apr 27, 2021 (155)
32 TOPMED ss5103257327 Apr 27, 2021 (155)
33 TOMMO_GENOMICS ss5231772529 Apr 27, 2021 (155)
34 1000G_HIGH_COVERAGE ss5310394208 Oct 16, 2022 (156)
35 EVA ss5440234616 Oct 16, 2022 (156)
36 HUGCELL_USP ss5502423591 Oct 16, 2022 (156)
37 1000G_HIGH_COVERAGE ss5617616754 Oct 16, 2022 (156)
38 SANFORD_IMAGENETICS ss5664123158 Oct 16, 2022 (156)
39 TOMMO_GENOMICS ss5792340952 Oct 16, 2022 (156)
40 EVA ss5892558670 Oct 16, 2022 (156)
41 EVA ss5959022964 Oct 16, 2022 (156)
42 1000Genomes NC_000021.8 - 45859042 Oct 12, 2018 (152)
43 1000Genomes_30x NC_000021.9 - 44439159 Oct 16, 2022 (156)
44 ExAC NC_000021.8 - 45859042 Oct 12, 2018 (152)
45 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 564555510 (NC_000021.9:44439158:C:G 1/140216)
Row 564555511 (NC_000021.9:44439158:C:T 1100/140214)

- Apr 27, 2021 (155)
46 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 564555510 (NC_000021.9:44439158:C:G 1/140216)
Row 564555511 (NC_000021.9:44439158:C:T 1100/140214)

- Apr 27, 2021 (155)
47 gnomAD - Exomes NC_000021.8 - 45859042 Jul 13, 2019 (153)
48 GO Exome Sequencing Project NC_000021.8 - 45859042 Oct 12, 2018 (152)
49 KOREAN population from KRGDB NC_000021.8 - 45859042 Apr 27, 2020 (154)
50 SGDP_PRJ NC_000021.8 - 45859042 Apr 27, 2020 (154)
51 8.3KJPN NC_000021.8 - 45859042 Apr 27, 2021 (155)
52 14KJPN NC_000021.9 - 44439159 Oct 16, 2022 (156)
53 TopMed

Submission ignored due to conflicting rows:
Row 378366272 (NC_000021.9:44439158:C:G 2/264690)
Row 378366273 (NC_000021.9:44439158:C:T 2228/264690)

- Apr 27, 2021 (155)
54 TopMed

Submission ignored due to conflicting rows:
Row 378366272 (NC_000021.9:44439158:C:G 2/264690)
Row 378366273 (NC_000021.9:44439158:C:T 2228/264690)

- Apr 27, 2021 (155)
55 ALFA NC_000021.9 - 44439159 Apr 27, 2021 (155)
56 ClinVar RCV000967576.3 Oct 16, 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).

Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
47650389, ss2704475166, ss3940472995 NC_000021.8:45859041:C:G NC_000021.9:44439158:C:G (self)
7255783849, ss2246176171, ss5103257326 NC_000021.9:44439158:C:G NC_000021.9:44439158:C:G (self)
ss204035302, ss484280859 NC_000021.7:44683469:C:T NC_000021.9:44439158:C:T (self)
80028952, 5752033, 14219822, 1870534, 42139561, 89741836, ss228595636, ss342534385, ss480256520, ss491186345, ss533636126, ss779187203, ss781185896, ss834652657, ss974511614, ss1067602636, ss1082541681, ss1366501125, ss1694183399, ss2633857103, ss2750474437, ss2972379565, ss3022165665, ss3628495540, ss3631810095, ss3652626895, ss3825413667, ss3890122581, ss3986848935, ss5231772529, ss5440234616, ss5664123158, ss5959022964 NC_000021.8:45859041:C:T NC_000021.9:44439158:C:T (self)
RCV000967576.3, 105142689, 126178056, 7255783849, ss2246176171, ss3725952920, ss3822340433, ss5103257327, ss5310394208, ss5502423591, ss5617616754, ss5792340952, ss5892558670 NC_000021.9:44439158:C:T NC_000021.9:44439158: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 rs79434849

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