SNP Links for Gene (Select 219958) - SNP

Links from Gene

Items: 1 to 20 of 1070

<< First< Prev

Page of 54

Next >Last >>

Select item 14867305081.

rs1486730508 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:58203470 (GRCh38)
11:57970942 (GRCh37)
Canonical SPDI:: NC_000011.10:58203469:C:T
Gene:: OR1S2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.58203470C>T, NC_000011.9:g.57970942C>T, NG_053130.1:g.5712G>A, NM_001004459.1:c.712G>A, NM_001004459.2:c.673G>A, NP_001004459.2:p.Val225Ile

Select item 14865246332.

rs1486524633 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 11:58205419 (GRCh38)
11:57972891 (GRCh37)
Canonical SPDI:: NC_000011.10:58205418:C:G
Gene:: OR1S2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000011.10:g.58205419C>G, NC_000011.9:g.57972891C>G, NG_053130.1:g.3763G>C

Select item 14864109883.

rs1486410988 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:58204599 (GRCh38)
11:57972071 (GRCh37)
Canonical SPDI:: NC_000011.10:58204598:C:T
Gene:: OR1S2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/1 (GnomAD)
T=0.000015/4 (TOPMED)
HGVS:: NC_000011.10:g.58204599C>T, NC_000011.9:g.57972071C>T, NG_053130.1:g.4583G>A

Select item 14854311114.

rs1485431111 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:58204216 (GRCh38)
11:57971688 (GRCh37)
Canonical SPDI:: NC_000011.10:58204215:G:A
Gene:: OR1S2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000011.10:g.58204216G>A, NC_000011.9:g.57971688G>A, NG_053130.1:g.4966C>T

Select item 14853698335.

rs1485369833 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:58203537 (GRCh38)
11:57971009 (GRCh37)
Canonical SPDI:: NC_000011.10:58203536:C:T
Gene:: OR1S2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.58203537C>T, NC_000011.9:g.57971009C>T, NG_053130.1:g.5645G>A, NM_001004459.1:c.645G>A, NM_001004459.2:c.606G>A

Select item 14851121726.

rs1485112172 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:58206061 (GRCh38)
11:57973533 (GRCh37)
Canonical SPDI:: NC_000011.10:58206060:G:A
Gene:: OR1S2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.58206061G>A, NC_000011.9:g.57973533G>A, NG_053130.1:g.3121C>T

Select item 14846896557.

rs1484689655 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 11:58205400 (GRCh38)
11:57972872 (GRCh37)
Canonical SPDI:: NC_000011.10:58205399:G:A,NC_000011.10:58205399:G:C
Gene:: OR1S2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000035/1 (TOMMO)
HGVS:: NC_000011.10:g.58205400G>A, NC_000011.10:g.58205400G>C, NC_000011.9:g.57972872G>A, NC_000011.9:g.57972872G>C, NG_053130.1:g.3782C>T, NG_053130.1:g.3782C>G

Select item 14843010118.

rs1484301011 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:58204042 (GRCh38)
11:57971514 (GRCh37)
Canonical SPDI:: NC_000011.10:58204041:A:G
Gene:: OR1S2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000028/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.58204042A>G, NC_000011.9:g.57971514A>G, NG_053130.1:g.5140T>C, NM_001004459.1:c.140T>C, NM_001004459.2:c.101T>C, NP_001004459.2:p.Met34Thr

Select item 14831865939.

rs1483186593 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 11:58205773 (GRCh38)
11:57973245 (GRCh37)
Canonical SPDI:: NC_000011.10:58205772:C:A,NC_000011.10:58205772:C:T
Gene:: OR1S2 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000021/3 (GnomAD)
HGVS:: NC_000011.10:g.58205773C>A, NC_000011.10:g.58205773C>T, NC_000011.9:g.57973245C>A, NC_000011.9:g.57973245C>T, NG_053130.1:g.3409G>T, NG_053130.1:g.3409G>A

Select item 148315694110.

rs1483156941 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:58205352 (GRCh38)
11:57972824 (GRCh37)
Canonical SPDI:: NC_000011.10:58205351:C:T
Gene:: OR1S2 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000035/1 (TOMMO)
HGVS:: NC_000011.10:g.58205352C>T, NC_000011.9:g.57972824C>T, NG_053130.1:g.3830G>A

Select item 148217897611.

rs1482178976 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:58205502 (GRCh38)
11:57972974 (GRCh37)
Canonical SPDI:: NC_000011.10:58205501:G:A
Gene:: OR1S2 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0./0 (GnomAD)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.58205502G>A, NC_000011.9:g.57972974G>A, NG_053130.1:g.3680C>T

Select item 148065984312.

rs1480659843 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:58205721 (GRCh38)
11:57973193 (GRCh37)
Canonical SPDI:: NC_000011.10:58205720:A:G
Gene:: OR1S2 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.58205721A>G, NC_000011.9:g.57973193A>G, NG_053130.1:g.3461T>C

Select item 147906717313.

rs1479067173 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:58202948 (GRCh38)
11:57970420 (GRCh37)
Canonical SPDI:: NC_000011.10:58202947:C:A
Gene:: OR1S2 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.58202948C>A, NC_000011.9:g.57970420C>A, NG_053130.1:g.6234G>T

Select item 147823427014.

rs1478234270 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 11:58203795 (GRCh38)
11:57971267 (GRCh37)
Canonical SPDI:: NC_000011.10:58203794:C:G
Gene:: OR1S2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: G=0.000012/3 (GnomAD_exomes)
HGVS:: NC_000011.10:g.58203795C>G, NC_000011.9:g.57971267C>G, NG_053130.1:g.5387G>C, NM_001004459.1:c.387G>C, NM_001004459.2:c.348G>C

Select item 147812998315.

rs1478129983 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 11:58202934 (GRCh38)
11:57970406 (GRCh37)
Canonical SPDI:: NC_000011.10:58202933:A:C,NC_000011.10:58202933:A:G
Gene:: OR1S2 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.58202934A>C, NC_000011.10:g.58202934A>G, NC_000011.9:g.57970406A>C, NC_000011.9:g.57970406A>G, NG_053130.1:g.6248T>G, NG_053130.1:g.6248T>C

Select item 147740524516.

rs1477405245 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:58205340 (GRCh38)
11:57972812 (GRCh37)
Canonical SPDI:: NC_000011.10:58205339:A:C
Gene:: OR1S2 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: C=0.000071/1 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.58205340A>C, NC_000011.9:g.57972812A>C, NG_053130.1:g.3842T>G

Select item 147718855317.

rs1477188553 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:58203021 (GRCh38)
11:57970493 (GRCh37)
Canonical SPDI:: NC_000011.10:58203020:A:G
Gene:: OR1S2 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.58203021A>G, NC_000011.9:g.57970493A>G, NG_053130.1:g.6161T>C

Select item 147658093418.

rs1476580934 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 11:58204537 (GRCh38)
11:57972009 (GRCh37)
Canonical SPDI:: NC_000011.10:58204536:C:G,NC_000011.10:58204536:C:T
Gene:: OR1S2 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
T=0.003765/11 (KOREAN)
HGVS:: NC_000011.10:g.58204537C>G, NC_000011.10:g.58204537C>T, NC_000011.9:g.57972009C>G, NC_000011.9:g.57972009C>T, NG_053130.1:g.4645G>C, NG_053130.1:g.4645G>A

Select item 147627727419.

rs1476277274 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:58203358 (GRCh38)
11:57970830 (GRCh37)
Canonical SPDI:: NC_000011.10:58203357:G:A
Gene:: OR1S2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.58203358G>A, NC_000011.9:g.57970830G>A, NG_053130.1:g.5824C>T, NM_001004459.1:c.824C>T, NM_001004459.2:c.785C>T, NP_001004459.2:p.Pro262Leu

Select item 147616610420.

rs1476166104 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:58202906 (GRCh38)
11:57970378 (GRCh37)
Canonical SPDI:: NC_000011.10:58202905:G:A,NC_000011.10:58202905:G:T
Gene:: OR1S2 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.58202906G>A, NC_000011.10:g.58202906G>T, NC_000011.9:g.57970378G>A, NC_000011.9:g.57970378G>T, NG_053130.1:g.6276C>T, NG_053130.1:g.6276C>A

dbSNP

Result Filters

Validation Status

Publication

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Gene

Items: 1 to 20 of 1070

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity