SNP Links for Protein (Select 52218834) - SNP

Links from Protein

Items: 1 to 20 of 359

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Select item 14889634461.

rs1488963446 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:15949383 (GRCh38)
19:16060193 (GRCh37)
Canonical SPDI:: NC_000019.10:15949382:G:A
Gene:: OR10H4 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.15949383G>A, NC_000019.9:g.16060193G>A, NM_001004465.1:c.376G>A, NP_001004465.1:p.Ala126Thr

Select item 14879375502.

rs1487937550 [Homo sapiens]

Variant type:: DEL
Alleles:: T>- [Show Flanks]
Chromosome:: 19:15949277 (GRCh38)
19:16060087 (GRCh37)
Canonical SPDI:: NC_000019.10:15949276:T:
Gene:: OR10H4 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.15949277del, NC_000019.9:g.16060087del, NM_001004465.1:c.270del, NP_001004465.1:p.His91fs

Select item 14877322843.

rs1487732284 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:15949949 (GRCh38)
19:16060759 (GRCh37)
Canonical SPDI:: NC_000019.10:15949948:A:G
Gene:: OR10H4 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000094/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.15949949A>G, NC_000019.9:g.16060759A>G, NM_001004465.1:c.942A>G

Select item 14857717594.

rs1485771759 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:15949379 (GRCh38)
19:16060189 (GRCh37)
Canonical SPDI:: NC_000019.10:15949378:T:C
Gene:: OR10H4 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.15949379T>C, NC_000019.9:g.16060189T>C, NM_001004465.1:c.372T>C

Select item 14853119245.

rs1485311924 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 19:15949178 (GRCh38)
19:16059988 (GRCh37)
Canonical SPDI:: NC_000019.10:15949177:C:A
Gene:: OR10H4 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0.000111/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.15949178C>A, NC_000019.9:g.16059988C>A, NM_001004465.1:c.171C>A, NP_001004465.1:p.His57Gln

Select item 14801005716.

rs1480100571 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:15949506 (GRCh38)
19:16060316 (GRCh37)
Canonical SPDI:: NC_000019.10:15949505:C:T
Gene:: OR10H4 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.15949506C>T, NC_000019.9:g.16060316C>T, NM_001004465.1:c.499C>T, NP_001004465.1:p.Leu167Phe

Select item 14789592297.

rs1478959229 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:15949601 (GRCh38)
19:16060411 (GRCh37)
Canonical SPDI:: NC_000019.10:15949600:C:T
Gene:: OR10H4 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000051/1 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000019.10:g.15949601C>T, NC_000019.9:g.16060411C>T, NM_001004465.1:c.594C>T

Select item 14732940078.

rs1473294007 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 19:15949764 (GRCh38)
19:16060574 (GRCh37)
Canonical SPDI:: NC_000019.10:15949763:C:G
Gene:: OR10H4 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0.000111/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.15949764C>G, NC_000019.9:g.16060574C>G, NM_001004465.1:c.757C>G, NP_001004465.1:p.His253Asp

Select item 14724356409.

rs1472435640 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:15949907 (GRCh38)
19:16060717 (GRCh37)
Canonical SPDI:: NC_000019.10:15949906:G:A
Gene:: OR10H4 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
A=0.001027/3 (KOREAN)
HGVS:: NC_000019.10:g.15949907G>A, NC_000019.9:g.16060717G>A, NM_001004465.1:c.900G>A

Select item 147133680510.

rs1471336805 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 19:15949203 (GRCh38)
19:16060013 (GRCh37)
Canonical SPDI:: NC_000019.10:15949202:A:C
Gene:: OR10H4 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.15949203A>C, NC_000019.9:g.16060013A>C, NM_001004465.1:c.196A>C, NP_001004465.1:p.Thr66Pro

Select item 146960922811.

rs1469609228 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:15949027 (GRCh38)
19:16059837 (GRCh37)
Canonical SPDI:: NC_000019.10:15949026:G:A
Gene:: OR10H4 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.15949027G>A, NC_000019.9:g.16059837G>A, NM_001004465.1:c.20G>A, NP_001004465.1:p.Ser7Asn

Select item 146604662412.

rs1466046624 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:15949276 (GRCh38)
19:16060086 (GRCh37)
Canonical SPDI:: NC_000019.10:15949275:A:G
Gene:: OR10H4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.15949276A>G, NC_000019.9:g.16060086A>G, NM_001004465.1:c.269A>G, NP_001004465.1:p.His90Arg

Select item 146223734613.

rs1462237346 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 19:15949063 (GRCh38)
19:16059873 (GRCh37)
Canonical SPDI:: NC_000019.10:15949062:C:A,NC_000019.10:15949062:C:G,NC_000019.10:15949062:C:T
Gene:: OR10H4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000019.10:g.15949063C>A, NC_000019.10:g.15949063C>G, NC_000019.10:g.15949063C>T, NC_000019.9:g.16059873C>A, NC_000019.9:g.16059873C>G, NC_000019.9:g.16059873C>T, NM_001004465.1:c.56C>A, NM_001004465.1:c.56C>G, NM_001004465.1:c.56C>T, NP_001004465.1:p.Ala19Asp, NP_001004465.1:p.Ala19Gly, NP_001004465.1:p.Ala19Val

Select item 146118916314.

rs1461189163 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 19:15949616 (GRCh38)
19:16060426 (GRCh37)
Canonical SPDI:: NC_000019.10:15949615:G:C
Gene:: OR10H4 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.15949616G>C, NC_000019.9:g.16060426G>C, NM_001004465.1:c.609G>C

Select item 145849849615.

rs1458498496 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:15949185 (GRCh38)
19:16059995 (GRCh37)
Canonical SPDI:: NC_000019.10:15949184:A:G
Gene:: OR10H4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
HGVS:: NC_000019.10:g.15949185A>G, NC_000019.9:g.16059995A>G, NM_001004465.1:c.178A>G, NP_001004465.1:p.Met60Val

Select item 145801813716.

rs1458018137 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 19:15949591 (GRCh38)
19:16060401 (GRCh37)
Canonical SPDI:: NC_000019.10:15949590:C:A
Gene:: OR10H4 (Varview)
Functional Consequence:: stop_gained,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.15949591C>A, NC_000019.9:g.16060401C>A, NM_001004465.1:c.584C>A, NP_001004465.1:p.Ser195Ter

Select item 144840988017.

rs1448409880 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:15949779 (GRCh38)
19:16060589 (GRCh37)
Canonical SPDI:: NC_000019.10:15949778:T:C
Gene:: OR10H4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.15949779T>C, NC_000019.9:g.16060589T>C, NM_001004465.1:c.772T>C, NP_001004465.1:p.Ser258Pro

Select item 144311976518.

rs1443119765 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:15949190 (GRCh38)
19:16060000 (GRCh37)
Canonical SPDI:: NC_000019.10:15949189:C:T
Gene:: OR10H4 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.15949190C>T, NC_000019.9:g.16060000C>T, NM_001004465.1:c.183C>T

Select item 144197826619.

rs1441978266 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 19:15949805 (GRCh38)
19:16060615 (GRCh37)
Canonical SPDI:: NC_000019.10:15949804:C:A
Gene:: OR10H4 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.15949805C>A, NC_000019.9:g.16060615C>A, NM_001004465.1:c.798C>A

Select item 144065777220.

rs1440657772 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 19:15949560 (GRCh38)
19:16060370 (GRCh37)
Canonical SPDI:: NC_000019.10:15949559:C:A
Gene:: OR10H4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0.000111/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.15949560C>A, NC_000019.9:g.16060370C>A, NM_001004465.1:c.553C>A, NP_001004465.1:p.Leu185Ile

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