SNP Links for Protein (Select 530360643) - SNP

Links from Protein

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Select item 14894727321.

rs1489472732 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:9129004 (GRCh38)
1:9189063 (GRCh37)
Canonical SPDI:: NC_000001.11:9129003:G:A
Gene:: GPR157 (Varview)
Functional Consequence:: non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
HGVS:: NC_000001.11:g.9129004G>A, NC_000001.10:g.9189063G>A, XM_005263496.6:c.24C>T, XM_005263496.5:c.24C>T, XM_005263496.4:c.24C>T, XM_005263496.3:c.24C>T, XM_005263496.2:c.24C>T, XM_005263496.1:c.24C>T, XM_005263497.6:c.24C>T, XM_005263497.5:c.24C>T, XM_005263497.4:c.24C>T, XM_005263497.3:c.24C>T, XM_005263497.2:c.24C>T, XM_005263497.1:c.24C>T, NM_024980.5:c.24C>T, NM_024980.4:c.24C>T, XR_007063977.1:n.99C>T

Select item 14880976292.

rs1488097629 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:9104457 (GRCh38)
1:9164516 (GRCh37)
Canonical SPDI:: NC_000001.11:9104456:C:G
Gene:: GPR157 (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.9104457C>G, NC_000001.10:g.9164516C>G, XM_005263496.6:c.931G>C, XM_005263496.5:c.931G>C, XM_005263496.4:c.931G>C, XM_005263496.3:c.931G>C, XM_005263496.2:c.931G>C, XM_005263496.1:c.931G>C, XM_005263497.6:c.775G>C, XM_005263497.5:c.775G>C, XM_005263497.4:c.775G>C, XM_005263497.3:c.775G>C, XM_005263497.2:c.775G>C, XM_005263497.1:c.775G>C, NM_024980.5:c.970G>C, NM_024980.4:c.970G>C, XR_007063977.1:n.1045G>C, XP_005263553.1:p.Glu311Gln, XP_005263554.1:p.Glu259Gln, NP_079256.4:p.Glu324Gln

Select item 14860652863.

rs1486065286 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 1:9104623 (GRCh38)
1:9164682 (GRCh37)
Canonical SPDI:: NC_000001.11:9104622:G:A,NC_000001.11:9104622:G:T
Gene:: GPR157 (Varview)
Functional Consequence:: non_coding_transcript_variant,synonymous_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.9104623G>A, NC_000001.11:g.9104623G>T, NC_000001.10:g.9164682G>A, NC_000001.10:g.9164682G>T, XM_005263496.6:c.765C>T, XM_005263496.6:c.765C>A, XM_005263496.5:c.765C>T, XM_005263496.5:c.765C>A, XM_005263496.4:c.765C>T, XM_005263496.4:c.765C>A, XM_005263496.3:c.765C>T, XM_005263496.3:c.765C>A, XM_005263496.2:c.765C>T, XM_005263496.2:c.765C>A, XM_005263496.1:c.765C>T, XM_005263496.1:c.765C>A, XM_005263497.6:c.609C>T, XM_005263497.6:c.609C>A, XM_005263497.5:c.609C>T, XM_005263497.5:c.609C>A, XM_005263497.4:c.609C>T, XM_005263497.4:c.609C>A, XM_005263497.3:c.609C>T, XM_005263497.3:c.609C>A, XM_005263497.2:c.609C>T, XM_005263497.2:c.609C>A, XM_005263497.1:c.609C>T, XM_005263497.1:c.609C>A, NM_024980.5:c.804C>T, NM_024980.5:c.804C>A, NM_024980.4:c.804C>T, NM_024980.4:c.804C>A, XR_007063977.1:n.879C>T, XR_007063977.1:n.879C>A, XP_005263553.1:p.Asn255Lys, XP_005263554.1:p.Asn203Lys, NP_079256.4:p.Asn268Lys

Select item 14836605494.

rs1483660549 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 1:9104424 (GRCh38)
1:9164483 (GRCh37)
Canonical SPDI:: NC_000001.11:9104423:T:G
Gene:: GPR157 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.9104424T>G, NC_000001.10:g.9164483T>G, XM_005263496.6:c.964A>C, XM_005263496.5:c.964A>C, XM_005263496.4:c.964A>C, XM_005263496.3:c.964A>C, XM_005263496.2:c.964A>C, XM_005263496.1:c.964A>C, XM_005263497.6:c.808A>C, XM_005263497.5:c.808A>C, XM_005263497.4:c.808A>C, XM_005263497.3:c.808A>C, XM_005263497.2:c.808A>C, XM_005263497.1:c.808A>C, NM_024980.5:c.1003A>C, NM_024980.4:c.1003A>C, XR_007063977.1:n.1078A>C, XP_005263553.1:p.Thr322Pro, XP_005263554.1:p.Thr270Pro, NP_079256.4:p.Thr335Pro

Select item 14831928095.

rs1483192809 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:9128724 (GRCh38)
1:9188783 (GRCh37)
Canonical SPDI:: NC_000001.11:9128723:G:A
Gene:: GPR157 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.9128724G>A, NC_000001.10:g.9188783G>A, XM_005263496.6:c.304C>T, XM_005263496.5:c.304C>T, XM_005263496.4:c.304C>T, XM_005263496.3:c.304C>T, XM_005263496.2:c.304C>T, XM_005263496.1:c.304C>T, XM_005263497.6:c.304C>T, XM_005263497.5:c.304C>T, XM_005263497.4:c.304C>T, XM_005263497.3:c.304C>T, XM_005263497.2:c.304C>T, XM_005263497.1:c.304C>T, NM_024980.5:c.304C>T, NM_024980.4:c.304C>T, XR_007063977.1:n.379C>T, XP_005263553.1:p.Leu102Phe, XP_005263554.1:p.Leu102Phe, NP_079256.4:p.Leu102Phe

Select item 14822238206.

rs1482223820 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 1:9129020 (GRCh38)
1:9189079 (GRCh37)
Canonical SPDI:: NC_000001.11:9129019:G:A,NC_000001.11:9129019:G:C,NC_000001.11:9129019:G:T
Gene:: GPR157 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.9129020G>A, NC_000001.11:g.9129020G>C, NC_000001.11:g.9129020G>T, NC_000001.10:g.9189079G>A, NC_000001.10:g.9189079G>C, NC_000001.10:g.9189079G>T, XM_005263496.6:c.8C>T, XM_005263496.6:c.8C>G, XM_005263496.6:c.8C>A, XM_005263496.5:c.8C>T, XM_005263496.5:c.8C>G, XM_005263496.5:c.8C>A, XM_005263496.4:c.8C>T, XM_005263496.4:c.8C>G, XM_005263496.4:c.8C>A, XM_005263496.3:c.8C>T, XM_005263496.3:c.8C>G, XM_005263496.3:c.8C>A, XM_005263496.2:c.8C>T, XM_005263496.2:c.8C>G, XM_005263496.2:c.8C>A, XM_005263496.1:c.8C>T, XM_005263496.1:c.8C>G, XM_005263496.1:c.8C>A, XM_005263497.6:c.8C>T, XM_005263497.6:c.8C>G, XM_005263497.6:c.8C>A, XM_005263497.5:c.8C>T, XM_005263497.5:c.8C>G, XM_005263497.5:c.8C>A, XM_005263497.4:c.8C>T, XM_005263497.4:c.8C>G, XM_005263497.4:c.8C>A, XM_005263497.3:c.8C>T, XM_005263497.3:c.8C>G, XM_005263497.3:c.8C>A, XM_005263497.2:c.8C>T, XM_005263497.2:c.8C>G, XM_005263497.2:c.8C>A, XM_005263497.1:c.8C>T, XM_005263497.1:c.8C>G, XM_005263497.1:c.8C>A, NM_024980.5:c.8C>T, NM_024980.5:c.8C>G, NM_024980.5:c.8C>A, NM_024980.4:c.8C>T, NM_024980.4:c.8C>G, NM_024980.4:c.8C>A, XR_007063977.1:n.83C>T, XR_007063977.1:n.83C>G, XR_007063977.1:n.83C>A, XP_005263553.1:p.Pro3Leu, XP_005263553.1:p.Pro3Arg, XP_005263553.1:p.Pro3Gln, XP_005263554.1:p.Pro3Leu, XP_005263554.1:p.Pro3Arg, XP_005263554.1:p.Pro3Gln, NP_079256.4:p.Pro3Leu, NP_079256.4:p.Pro3Arg, NP_079256.4:p.Pro3Gln

Select item 14765319957.

rs1476531995 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:9104490 (GRCh38)
1:9164549 (GRCh37)
Canonical SPDI:: NC_000001.11:9104489:C:T
Gene:: GPR157 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.9104490C>T, NC_000001.10:g.9164549C>T, XM_005263496.6:c.898G>A, XM_005263496.5:c.898G>A, XM_005263496.4:c.898G>A, XM_005263496.3:c.898G>A, XM_005263496.2:c.898G>A, XM_005263496.1:c.898G>A, XM_005263497.6:c.742G>A, XM_005263497.5:c.742G>A, XM_005263497.4:c.742G>A, XM_005263497.3:c.742G>A, XM_005263497.2:c.742G>A, XM_005263497.1:c.742G>A, NM_024980.5:c.937G>A, NM_024980.4:c.937G>A, XR_007063977.1:n.1012G>A, XP_005263553.1:p.Ala300Thr, XP_005263554.1:p.Ala248Thr, NP_079256.4:p.Ala313Thr

Select item 14744127068.

rs1474412706 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:9128823 (GRCh38)
1:9188882 (GRCh37)
Canonical SPDI:: NC_000001.11:9128822:G:A
Gene:: GPR157 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,non_coding_transcript_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_000001.11:g.9128823G>A, NC_000001.10:g.9188882G>A, XM_005263496.6:c.205C>T, XM_005263496.5:c.205C>T, XM_005263496.4:c.205C>T, XM_005263496.3:c.205C>T, XM_005263496.2:c.205C>T, XM_005263496.1:c.205C>T, XM_005263497.6:c.205C>T, XM_005263497.5:c.205C>T, XM_005263497.4:c.205C>T, XM_005263497.3:c.205C>T, XM_005263497.2:c.205C>T, XM_005263497.1:c.205C>T, NM_024980.5:c.205C>T, NM_024980.4:c.205C>T, XR_007063977.1:n.280C>T

Select item 14717917069.

rs1471791706 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:9128941 (GRCh38)
1:9189000 (GRCh37)
Canonical SPDI:: NC_000001.11:9128940:C:T
Gene:: GPR157 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,non_coding_transcript_variant
Validated:: by frequency
MAF:: T=0.000008/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.9128941C>T, NC_000001.10:g.9189000C>T, XM_005263496.6:c.87G>A, XM_005263496.5:c.87G>A, XM_005263496.4:c.87G>A, XM_005263496.3:c.87G>A, XM_005263496.2:c.87G>A, XM_005263496.1:c.87G>A, XM_005263497.6:c.87G>A, XM_005263497.5:c.87G>A, XM_005263497.4:c.87G>A, XM_005263497.3:c.87G>A, XM_005263497.2:c.87G>A, XM_005263497.1:c.87G>A, NM_024980.5:c.87G>A, NM_024980.4:c.87G>A, XR_007063977.1:n.162G>A

Select item 146912702810.

rs1469127028 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:9111282 (GRCh38)
1:9171341 (GRCh37)
Canonical SPDI:: NC_000001.11:9111281:G:A
Gene:: GPR157 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.9111282G>A, NC_000001.10:g.9171341G>A, XM_005263496.6:c.591C>T, XM_005263496.5:c.591C>T, XM_005263496.4:c.591C>T, XM_005263496.3:c.591C>T, XM_005263496.2:c.591C>T, XM_005263496.1:c.591C>T, XM_005263497.6:c.591C>T, XM_005263497.5:c.591C>T, XM_005263497.4:c.591C>T, XM_005263497.3:c.591C>T, XM_005263497.2:c.591C>T, XM_005263497.1:c.591C>T, NM_024980.5:c.591C>T, NM_024980.4:c.591C>T, XR_007063977.1:n.666C>T

Select item 146086896611.

rs1460868966 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 1:9104511 (GRCh38)
1:9164570 (GRCh37)
Canonical SPDI:: NC_000001.11:9104510:T:A
Gene:: GPR157 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,non_coding_transcript_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_000001.11:g.9104511T>A, NC_000001.10:g.9164570T>A, XM_005263496.6:c.877A>T, XM_005263496.5:c.877A>T, XM_005263496.4:c.877A>T, XM_005263496.3:c.877A>T, XM_005263496.2:c.877A>T, XM_005263496.1:c.877A>T, XM_005263497.6:c.721A>T, XM_005263497.5:c.721A>T, XM_005263497.4:c.721A>T, XM_005263497.3:c.721A>T, XM_005263497.2:c.721A>T, XM_005263497.1:c.721A>T, NM_024980.5:c.916A>T, NM_024980.4:c.916A>T, XR_007063977.1:n.991A>T, XP_005263553.1:p.Ser293Cys, XP_005263554.1:p.Ser241Cys, NP_079256.4:p.Ser306Cys

Select item 145610099312.

rs1456100993 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:9128889 (GRCh38)
1:9188948 (GRCh37)
Canonical SPDI:: NC_000001.11:9128888:G:A
Gene:: GPR157 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD_exomes)
A=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.9128889G>A, NC_000001.10:g.9188948G>A, XM_005263496.6:c.139C>T, XM_005263496.5:c.139C>T, XM_005263496.4:c.139C>T, XM_005263496.3:c.139C>T, XM_005263496.2:c.139C>T, XM_005263496.1:c.139C>T, XM_005263497.6:c.139C>T, XM_005263497.5:c.139C>T, XM_005263497.4:c.139C>T, XM_005263497.3:c.139C>T, XM_005263497.2:c.139C>T, XM_005263497.1:c.139C>T, NM_024980.5:c.139C>T, NM_024980.4:c.139C>T, XR_007063977.1:n.214C>T, XP_005263553.1:p.Arg47Trp, XP_005263554.1:p.Arg47Trp, NP_079256.4:p.Arg47Trp

Select item 145587308513.

rs1455873085 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:9128912 (GRCh38)
1:9188971 (GRCh37)
Canonical SPDI:: NC_000001.11:9128911:C:A
Gene:: GPR157 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_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_000001.11:g.9128912C>A, NC_000001.10:g.9188971C>A, XM_005263496.6:c.116G>T, XM_005263496.5:c.116G>T, XM_005263496.4:c.116G>T, XM_005263496.3:c.116G>T, XM_005263496.2:c.116G>T, XM_005263496.1:c.116G>T, XM_005263497.6:c.116G>T, XM_005263497.5:c.116G>T, XM_005263497.4:c.116G>T, XM_005263497.3:c.116G>T, XM_005263497.2:c.116G>T, XM_005263497.1:c.116G>T, NM_024980.5:c.116G>T, NM_024980.4:c.116G>T, XR_007063977.1:n.191G>T, XP_005263553.1:p.Trp39Leu, XP_005263554.1:p.Trp39Leu, NP_079256.4:p.Trp39Leu

Select item 145378682814.

rs1453786828 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:9111322 (GRCh38)
1:9171381 (GRCh37)
Canonical SPDI:: NC_000001.11:9111321:A:G
Gene:: GPR157 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0./0 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.9111322A>G, NC_000001.10:g.9171381A>G, XM_005263496.6:c.551T>C, XM_005263496.5:c.551T>C, XM_005263496.4:c.551T>C, XM_005263496.3:c.551T>C, XM_005263496.2:c.551T>C, XM_005263496.1:c.551T>C, XM_005263497.6:c.551T>C, XM_005263497.5:c.551T>C, XM_005263497.4:c.551T>C, XM_005263497.3:c.551T>C, XM_005263497.2:c.551T>C, XM_005263497.1:c.551T>C, NM_024980.5:c.551T>C, NM_024980.4:c.551T>C, XR_007063977.1:n.626T>C, XP_005263553.1:p.Leu184Pro, XP_005263554.1:p.Leu184Pro, NP_079256.4:p.Leu184Pro

Select item 145353964715.

rs1453539647 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:9128938 (GRCh38)
1:9188997 (GRCh37)
Canonical SPDI:: NC_000001.11:9128937:G:T
Gene:: GPR157 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.9128938G>T, NC_000001.10:g.9188997G>T, XM_005263496.6:c.90C>A, XM_005263496.5:c.90C>A, XM_005263496.4:c.90C>A, XM_005263496.3:c.90C>A, XM_005263496.2:c.90C>A, XM_005263496.1:c.90C>A, XM_005263497.6:c.90C>A, XM_005263497.5:c.90C>A, XM_005263497.4:c.90C>A, XM_005263497.3:c.90C>A, XM_005263497.2:c.90C>A, XM_005263497.1:c.90C>A, NM_024980.5:c.90C>A, NM_024980.4:c.90C>A, XR_007063977.1:n.165C>A

Select item 145009676216.

rs1450096762 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:9128872 (GRCh38)
1:9188931 (GRCh37)
Canonical SPDI:: NC_000001.11:9128871:G:A
Gene:: GPR157 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,synonymous_variant
HGVS:: NC_000001.11:g.9128872G>A, NC_000001.10:g.9188931G>A, XM_005263496.6:c.156C>T, XM_005263496.5:c.156C>T, XM_005263496.4:c.156C>T, XM_005263496.3:c.156C>T, XM_005263496.2:c.156C>T, XM_005263496.1:c.156C>T, XM_005263497.6:c.156C>T, XM_005263497.5:c.156C>T, XM_005263497.4:c.156C>T, XM_005263497.3:c.156C>T, XM_005263497.2:c.156C>T, XM_005263497.1:c.156C>T, NM_024980.5:c.156C>T, NM_024980.4:c.156C>T, XR_007063977.1:n.231C>T

Select item 144520116017.

rs1445201160 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:9128869 (GRCh38)
1:9188928 (GRCh37)
Canonical SPDI:: NC_000001.11:9128868:C:T
Gene:: GPR157 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000001.11:g.9128869C>T, NC_000001.10:g.9188928C>T, XM_005263496.6:c.159G>A, XM_005263496.5:c.159G>A, XM_005263496.4:c.159G>A, XM_005263496.3:c.159G>A, XM_005263496.2:c.159G>A, XM_005263496.1:c.159G>A, XM_005263497.6:c.159G>A, XM_005263497.5:c.159G>A, XM_005263497.4:c.159G>A, XM_005263497.3:c.159G>A, XM_005263497.2:c.159G>A, XM_005263497.1:c.159G>A, NM_024980.5:c.159G>A, NM_024980.4:c.159G>A, XR_007063977.1:n.234G>A

Select item 144501341318.

rs1445013413 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:9111479 (GRCh38)
1:9171538 (GRCh37)
Canonical SPDI:: NC_000001.11:9111478:G:T
Gene:: GPR157 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.9111479G>T, NC_000001.10:g.9171538G>T, XM_005263496.6:c.394C>A, XM_005263496.5:c.394C>A, XM_005263496.4:c.394C>A, XM_005263496.3:c.394C>A, XM_005263496.2:c.394C>A, XM_005263496.1:c.394C>A, XM_005263497.6:c.394C>A, XM_005263497.5:c.394C>A, XM_005263497.4:c.394C>A, XM_005263497.3:c.394C>A, XM_005263497.2:c.394C>A, XM_005263497.1:c.394C>A, NM_024980.5:c.394C>A, NM_024980.4:c.394C>A, XR_007063977.1:n.469C>A, XP_005263553.1:p.Pro132Thr, XP_005263554.1:p.Pro132Thr, NP_079256.4:p.Pro132Thr

Select item 144295776419.

rs1442957764 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:9128989 (GRCh38)
1:9189048 (GRCh37)
Canonical SPDI:: NC_000001.11:9128988:C:T
Gene:: GPR157 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.9128989C>T, NC_000001.10:g.9189048C>T, XM_005263496.6:c.39G>A, XM_005263496.5:c.39G>A, XM_005263496.4:c.39G>A, XM_005263496.3:c.39G>A, XM_005263496.2:c.39G>A, XM_005263496.1:c.39G>A, XM_005263497.6:c.39G>A, XM_005263497.5:c.39G>A, XM_005263497.4:c.39G>A, XM_005263497.3:c.39G>A, XM_005263497.2:c.39G>A, XM_005263497.1:c.39G>A, NM_024980.5:c.39G>A, NM_024980.4:c.39G>A, XR_007063977.1:n.114G>A

Select item 144151705220.

rs1441517052 [Homo sapiens]

Variant type:: DELINS
Alleles:: G>- [Show Flanks]
Chromosome:: 1:9111302 (GRCh38)
1:9171361 (GRCh37)
Canonical SPDI:: NC_000001.11:9111301:GG:G
Gene:: GPR157 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant,non_coding_transcript_variant
Validated:: by frequency
MAF:: -=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.9111303del, NC_000001.10:g.9171362del, XM_005263496.6:c.571del, XM_005263496.5:c.571del, XM_005263496.4:c.571del, XM_005263496.3:c.571del, XM_005263496.2:c.571del, XM_005263496.1:c.571del, XM_005263497.6:c.571del, XM_005263497.5:c.571del, XM_005263497.4:c.571del, XM_005263497.3:c.571del, XM_005263497.2:c.571del, XM_005263497.1:c.571del, NM_024980.5:c.571del, NM_024980.4:c.571del, XR_007063977.1:n.646del, XP_005263553.1:p.Leu191fs, XP_005263554.1:p.Leu191fs, NP_079256.4:p.Leu191fs

dbSNP

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