SNP Links for Protein (Select 13540557) - SNP

Links from Protein

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Select item 14884658341.

rs1488465834 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,T [Show Flanks]
Chromosome:: 6:96798615 (GRCh38)
6:97246491 (GRCh37)
Canonical SPDI:: NC_000006.12:96798614:A:C,NC_000006.12:96798614:A:T
Gene:: GPR63 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
C=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.96798615A>C, NC_000006.12:g.96798615A>T, NC_000006.11:g.97246491A>C, NC_000006.11:g.97246491A>T, XM_006715570.5:c.1117T>G, XM_006715570.5:c.1117T>A, XM_006715570.4:c.1117T>G, XM_006715570.4:c.1117T>A, XM_006715570.3:c.1117T>G, XM_006715570.3:c.1117T>A, XM_006715570.2:c.1117T>G, XM_006715570.2:c.1117T>A, XM_006715570.1:c.1117T>G, XM_006715570.1:c.1117T>A, NM_030784.4:c.1117T>G, NM_030784.4:c.1117T>A, NM_030784.3:c.1117T>G, NM_030784.3:c.1117T>A, NM_001143957.3:c.1117T>G, NM_001143957.3:c.1117T>A, NM_001143957.2:c.1117T>G, NM_001143957.2:c.1117T>A, XM_011536157.3:c.1117T>G, XM_011536157.3:c.1117T>A, XM_011536157.2:c.1117T>G, XM_011536157.2:c.1117T>A, XM_011536157.1:c.1117T>G, XM_011536157.1:c.1117T>A, XM_011536154.3:c.1117T>G, XM_011536154.3:c.1117T>A, XM_011536154.2:c.1117T>G, XM_011536154.2:c.1117T>A, XM_011536154.1:c.1117T>G, XM_011536154.1:c.1117T>A, XM_017011334.2:c.1117T>G, XM_017011334.2:c.1117T>A, XM_017011334.1:c.1117T>G, XM_017011334.1:c.1117T>A, XM_011536155.2:c.1117T>G, XM_011536155.2:c.1117T>A, XM_011536155.1:c.1117T>G, XM_011536155.1:c.1117T>A, XM_011536153.2:c.1117T>G, XM_011536153.2:c.1117T>A, XM_011536153.1:c.1117T>G, XM_011536153.1:c.1117T>A, XM_011536159.2:c.1117T>G, XM_011536159.2:c.1117T>A, XM_011536159.1:c.1117T>G, XM_011536159.1:c.1117T>A, XP_006715633.1:p.Trp373Gly, XP_006715633.1:p.Trp373Arg, NP_110411.1:p.Trp373Gly, NP_110411.1:p.Trp373Arg, NP_001137429.1:p.Trp373Gly, NP_001137429.1:p.Trp373Arg, XP_011534459.1:p.Trp373Gly, XP_011534459.1:p.Trp373Arg, XP_011534456.1:p.Trp373Gly, XP_011534456.1:p.Trp373Arg, XP_016866823.1:p.Trp373Gly, XP_016866823.1:p.Trp373Arg, XP_011534457.1:p.Trp373Gly, XP_011534457.1:p.Trp373Arg, XP_011534455.1:p.Trp373Gly, XP_011534455.1:p.Trp373Arg, XP_011534461.1:p.Trp373Gly, XP_011534461.1:p.Trp373Arg

Select item 14865638662.

rs1486563866 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 6:96799331 (GRCh38)
6:97247207 (GRCh37)
Canonical SPDI:: NC_000006.12:96799330:T:G
Gene:: GPR63 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000283/5 (TOMMO)
HGVS:: NC_000006.12:g.96799331T>G, NC_000006.11:g.97247207T>G, XM_006715570.5:c.401A>C, XM_006715570.4:c.401A>C, XM_006715570.3:c.401A>C, XM_006715570.2:c.401A>C, XM_006715570.1:c.401A>C, NM_030784.4:c.401A>C, NM_030784.3:c.401A>C, NM_001143957.3:c.401A>C, NM_001143957.2:c.401A>C, XM_011536157.3:c.401A>C, XM_011536157.2:c.401A>C, XM_011536157.1:c.401A>C, XM_011536154.3:c.401A>C, XM_011536154.2:c.401A>C, XM_011536154.1:c.401A>C, XM_017011334.2:c.401A>C, XM_017011334.1:c.401A>C, XM_011536155.2:c.401A>C, XM_011536155.1:c.401A>C, XM_011536153.2:c.401A>C, XM_011536153.1:c.401A>C, XM_011536159.2:c.401A>C, XM_011536159.1:c.401A>C, XP_006715633.1:p.Asn134Thr, NP_110411.1:p.Asn134Thr, NP_001137429.1:p.Asn134Thr, XP_011534459.1:p.Asn134Thr, XP_011534456.1:p.Asn134Thr, XP_016866823.1:p.Asn134Thr, XP_011534457.1:p.Asn134Thr, XP_011534455.1:p.Asn134Thr, XP_011534461.1:p.Asn134Thr

Select item 14862183413.

rs1486218341 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:96799198 (GRCh38)
6:97247074 (GRCh37)
Canonical SPDI:: NC_000006.12:96799197:A:G
Gene:: GPR63 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
G=0.000012/3 (GnomAD_exomes)
HGVS:: NC_000006.12:g.96799198A>G, NC_000006.11:g.97247074A>G, XM_006715570.5:c.534T>C, XM_006715570.4:c.534T>C, XM_006715570.3:c.534T>C, XM_006715570.2:c.534T>C, XM_006715570.1:c.534T>C, NM_030784.4:c.534T>C, NM_030784.3:c.534T>C, NM_001143957.3:c.534T>C, NM_001143957.2:c.534T>C, XM_011536157.3:c.534T>C, XM_011536157.2:c.534T>C, XM_011536157.1:c.534T>C, XM_011536154.3:c.534T>C, XM_011536154.2:c.534T>C, XM_011536154.1:c.534T>C, XM_017011334.2:c.534T>C, XM_017011334.1:c.534T>C, XM_011536155.2:c.534T>C, XM_011536155.1:c.534T>C, XM_011536153.2:c.534T>C, XM_011536153.1:c.534T>C, XM_011536159.2:c.534T>C, XM_011536159.1:c.534T>C

Select item 14860214454.

rs1486021445 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:96799485 (GRCh38)
6:97247361 (GRCh37)
Canonical SPDI:: NC_000006.12:96799484:T:C
Gene:: GPR63 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.96799485T>C, NC_000006.11:g.97247361T>C, XM_006715570.5:c.247A>G, XM_006715570.4:c.247A>G, XM_006715570.3:c.247A>G, XM_006715570.2:c.247A>G, XM_006715570.1:c.247A>G, NM_030784.4:c.247A>G, NM_030784.3:c.247A>G, NM_001143957.3:c.247A>G, NM_001143957.2:c.247A>G, XM_011536157.3:c.247A>G, XM_011536157.2:c.247A>G, XM_011536157.1:c.247A>G, XM_011536154.3:c.247A>G, XM_011536154.2:c.247A>G, XM_011536154.1:c.247A>G, XM_017011334.2:c.247A>G, XM_017011334.1:c.247A>G, XM_011536155.2:c.247A>G, XM_011536155.1:c.247A>G, XM_011536153.2:c.247A>G, XM_011536153.1:c.247A>G, XM_011536159.2:c.247A>G, XM_011536159.1:c.247A>G, XP_006715633.1:p.Thr83Ala, NP_110411.1:p.Thr83Ala, NP_001137429.1:p.Thr83Ala, XP_011534459.1:p.Thr83Ala, XP_011534456.1:p.Thr83Ala, XP_016866823.1:p.Thr83Ala, XP_011534457.1:p.Thr83Ala, XP_011534455.1:p.Thr83Ala, XP_011534461.1:p.Thr83Ala

Select item 14853651535.

rs1485365153 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:96799349 (GRCh38)
6:97247225 (GRCh37)
Canonical SPDI:: NC_000006.12:96799348:A:G
Gene:: GPR63 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0.000028/1 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000006.12:g.96799349A>G, NC_000006.11:g.97247225A>G, XM_006715570.5:c.383T>C, XM_006715570.4:c.383T>C, XM_006715570.3:c.383T>C, XM_006715570.2:c.383T>C, XM_006715570.1:c.383T>C, NM_030784.4:c.383T>C, NM_030784.3:c.383T>C, NM_001143957.3:c.383T>C, NM_001143957.2:c.383T>C, XM_011536157.3:c.383T>C, XM_011536157.2:c.383T>C, XM_011536157.1:c.383T>C, XM_011536154.3:c.383T>C, XM_011536154.2:c.383T>C, XM_011536154.1:c.383T>C, XM_017011334.2:c.383T>C, XM_017011334.1:c.383T>C, XM_011536155.2:c.383T>C, XM_011536155.1:c.383T>C, XM_011536153.2:c.383T>C, XM_011536153.1:c.383T>C, XM_011536159.2:c.383T>C, XM_011536159.1:c.383T>C, XP_006715633.1:p.Met128Thr, NP_110411.1:p.Met128Thr, NP_001137429.1:p.Met128Thr, XP_011534459.1:p.Met128Thr, XP_011534456.1:p.Met128Thr, XP_016866823.1:p.Met128Thr, XP_011534457.1:p.Met128Thr, XP_011534455.1:p.Met128Thr, XP_011534461.1:p.Met128Thr

Select item 14849284646.

rs1484928464 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 6:96798679 (GRCh38)
6:97246555 (GRCh37)
Canonical SPDI:: NC_000006.12:96798678:C:G,NC_000006.12:96798678:C:T
Gene:: GPR63 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.96798679C>G, NC_000006.12:g.96798679C>T, NC_000006.11:g.97246555C>G, NC_000006.11:g.97246555C>T, XM_006715570.5:c.1053G>C, XM_006715570.5:c.1053G>A, XM_006715570.4:c.1053G>C, XM_006715570.4:c.1053G>A, XM_006715570.3:c.1053G>C, XM_006715570.3:c.1053G>A, XM_006715570.2:c.1053G>C, XM_006715570.2:c.1053G>A, XM_006715570.1:c.1053G>C, XM_006715570.1:c.1053G>A, NM_030784.4:c.1053G>C, NM_030784.4:c.1053G>A, NM_030784.3:c.1053G>C, NM_030784.3:c.1053G>A, NM_001143957.3:c.1053G>C, NM_001143957.3:c.1053G>A, NM_001143957.2:c.1053G>C, NM_001143957.2:c.1053G>A, XM_011536157.3:c.1053G>C, XM_011536157.3:c.1053G>A, XM_011536157.2:c.1053G>C, XM_011536157.2:c.1053G>A, XM_011536157.1:c.1053G>C, XM_011536157.1:c.1053G>A, XM_011536154.3:c.1053G>C, XM_011536154.3:c.1053G>A, XM_011536154.2:c.1053G>C, XM_011536154.2:c.1053G>A, XM_011536154.1:c.1053G>C, XM_011536154.1:c.1053G>A, XM_017011334.2:c.1053G>C, XM_017011334.2:c.1053G>A, XM_017011334.1:c.1053G>C, XM_017011334.1:c.1053G>A, XM_011536155.2:c.1053G>C, XM_011536155.2:c.1053G>A, XM_011536155.1:c.1053G>C, XM_011536155.1:c.1053G>A, XM_011536153.2:c.1053G>C, XM_011536153.2:c.1053G>A, XM_011536153.1:c.1053G>C, XM_011536153.1:c.1053G>A, XM_011536159.2:c.1053G>C, XM_011536159.2:c.1053G>A, XM_011536159.1:c.1053G>C, XM_011536159.1:c.1053G>A, XP_006715633.1:p.Glu351Asp, NP_110411.1:p.Glu351Asp, NP_001137429.1:p.Glu351Asp, XP_011534459.1:p.Glu351Asp, XP_011534456.1:p.Glu351Asp, XP_016866823.1:p.Glu351Asp, XP_011534457.1:p.Glu351Asp, XP_011534455.1:p.Glu351Asp, XP_011534461.1:p.Glu351Asp

Select item 14845815207.

rs1484581520 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 6:96798819 (GRCh38)
6:97246695 (GRCh37)
Canonical SPDI:: NC_000006.12:96798818:C:A
Gene:: GPR63 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.96798819C>A, NC_000006.11:g.97246695C>A, XM_006715570.5:c.913G>T, XM_006715570.4:c.913G>T, XM_006715570.3:c.913G>T, XM_006715570.2:c.913G>T, XM_006715570.1:c.913G>T, NM_030784.4:c.913G>T, NM_030784.3:c.913G>T, NM_001143957.3:c.913G>T, NM_001143957.2:c.913G>T, XM_011536157.3:c.913G>T, XM_011536157.2:c.913G>T, XM_011536157.1:c.913G>T, XM_011536154.3:c.913G>T, XM_011536154.2:c.913G>T, XM_011536154.1:c.913G>T, XM_017011334.2:c.913G>T, XM_017011334.1:c.913G>T, XM_011536155.2:c.913G>T, XM_011536155.1:c.913G>T, XM_011536153.2:c.913G>T, XM_011536153.1:c.913G>T, XM_011536159.2:c.913G>T, XM_011536159.1:c.913G>T, XP_006715633.1:p.Asp305Tyr, NP_110411.1:p.Asp305Tyr, NP_001137429.1:p.Asp305Tyr, XP_011534459.1:p.Asp305Tyr, XP_011534456.1:p.Asp305Tyr, XP_016866823.1:p.Asp305Tyr, XP_011534457.1:p.Asp305Tyr, XP_011534455.1:p.Asp305Tyr, XP_011534461.1:p.Asp305Tyr

Select item 14840681478.

rs1484068147 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:96798691 (GRCh38)
6:97246567 (GRCh37)
Canonical SPDI:: NC_000006.12:96798690:G:A
Gene:: GPR63 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.96798691G>A, NC_000006.11:g.97246567G>A, XM_006715570.5:c.1041C>T, XM_006715570.4:c.1041C>T, XM_006715570.3:c.1041C>T, XM_006715570.2:c.1041C>T, XM_006715570.1:c.1041C>T, NM_030784.4:c.1041C>T, NM_030784.3:c.1041C>T, NM_001143957.3:c.1041C>T, NM_001143957.2:c.1041C>T, XM_011536157.3:c.1041C>T, XM_011536157.2:c.1041C>T, XM_011536157.1:c.1041C>T, XM_011536154.3:c.1041C>T, XM_011536154.2:c.1041C>T, XM_011536154.1:c.1041C>T, XM_017011334.2:c.1041C>T, XM_017011334.1:c.1041C>T, XM_011536155.2:c.1041C>T, XM_011536155.1:c.1041C>T, XM_011536153.2:c.1041C>T, XM_011536153.1:c.1041C>T, XM_011536159.2:c.1041C>T, XM_011536159.1:c.1041C>T

Select item 14799830629.

rs1479983062 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:96799395 (GRCh38)
6:97247271 (GRCh37)
Canonical SPDI:: NC_000006.12:96799394:T:C
Gene:: GPR63 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.96799395T>C, NC_000006.11:g.97247271T>C, XM_006715570.5:c.337A>G, XM_006715570.4:c.337A>G, XM_006715570.3:c.337A>G, XM_006715570.2:c.337A>G, XM_006715570.1:c.337A>G, NM_030784.4:c.337A>G, NM_030784.3:c.337A>G, NM_001143957.3:c.337A>G, NM_001143957.2:c.337A>G, XM_011536157.3:c.337A>G, XM_011536157.2:c.337A>G, XM_011536157.1:c.337A>G, XM_011536154.3:c.337A>G, XM_011536154.2:c.337A>G, XM_011536154.1:c.337A>G, XM_017011334.2:c.337A>G, XM_017011334.1:c.337A>G, XM_011536155.2:c.337A>G, XM_011536155.1:c.337A>G, XM_011536153.2:c.337A>G, XM_011536153.1:c.337A>G, XM_011536159.2:c.337A>G, XM_011536159.1:c.337A>G, XP_006715633.1:p.Arg113Gly, NP_110411.1:p.Arg113Gly, NP_001137429.1:p.Arg113Gly, XP_011534459.1:p.Arg113Gly, XP_011534456.1:p.Arg113Gly, XP_016866823.1:p.Arg113Gly, XP_011534457.1:p.Arg113Gly, XP_011534455.1:p.Arg113Gly, XP_011534461.1:p.Arg113Gly

Select item 147805392810.

rs1478053928 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:96799045 (GRCh38)
6:97246921 (GRCh37)
Canonical SPDI:: NC_000006.12:96799044:A:G
Gene:: GPR63 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_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_000006.12:g.96799045A>G, NC_000006.11:g.97246921A>G, XM_006715570.5:c.687T>C, XM_006715570.4:c.687T>C, XM_006715570.3:c.687T>C, XM_006715570.2:c.687T>C, XM_006715570.1:c.687T>C, NM_030784.4:c.687T>C, NM_030784.3:c.687T>C, NM_001143957.3:c.687T>C, NM_001143957.2:c.687T>C, XM_011536157.3:c.687T>C, XM_011536157.2:c.687T>C, XM_011536157.1:c.687T>C, XM_011536154.3:c.687T>C, XM_011536154.2:c.687T>C, XM_011536154.1:c.687T>C, XM_017011334.2:c.687T>C, XM_017011334.1:c.687T>C, XM_011536155.2:c.687T>C, XM_011536155.1:c.687T>C, XM_011536153.2:c.687T>C, XM_011536153.1:c.687T>C, XM_011536159.2:c.687T>C, XM_011536159.1:c.687T>C

Select item 147441246611.

rs1474412466 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 6:96798908 (GRCh38)
6:97246784 (GRCh37)
Canonical SPDI:: NC_000006.12:96798907:C:G
Gene:: GPR63 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.96798908C>G, NC_000006.11:g.97246784C>G, XM_006715570.5:c.824G>C, XM_006715570.4:c.824G>C, XM_006715570.3:c.824G>C, XM_006715570.2:c.824G>C, XM_006715570.1:c.824G>C, NM_030784.4:c.824G>C, NM_030784.3:c.824G>C, NM_001143957.3:c.824G>C, NM_001143957.2:c.824G>C, XM_011536157.3:c.824G>C, XM_011536157.2:c.824G>C, XM_011536157.1:c.824G>C, XM_011536154.3:c.824G>C, XM_011536154.2:c.824G>C, XM_011536154.1:c.824G>C, XM_017011334.2:c.824G>C, XM_017011334.1:c.824G>C, XM_011536155.2:c.824G>C, XM_011536155.1:c.824G>C, XM_011536153.2:c.824G>C, XM_011536153.1:c.824G>C, XM_011536159.2:c.824G>C, XM_011536159.1:c.824G>C, XP_006715633.1:p.Arg275Thr, NP_110411.1:p.Arg275Thr, NP_001137429.1:p.Arg275Thr, XP_011534459.1:p.Arg275Thr, XP_011534456.1:p.Arg275Thr, XP_016866823.1:p.Arg275Thr, XP_011534457.1:p.Arg275Thr, XP_011534455.1:p.Arg275Thr, XP_011534461.1:p.Arg275Thr

Select item 147414804912.

rs1474148049 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:96798722 (GRCh38)
6:97246598 (GRCh37)
Canonical SPDI:: NC_000006.12:96798721:G:A
Gene:: GPR63 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.96798722G>A, NC_000006.11:g.97246598G>A, XM_006715570.5:c.1010C>T, XM_006715570.4:c.1010C>T, XM_006715570.3:c.1010C>T, XM_006715570.2:c.1010C>T, XM_006715570.1:c.1010C>T, NM_030784.4:c.1010C>T, NM_030784.3:c.1010C>T, NM_001143957.3:c.1010C>T, NM_001143957.2:c.1010C>T, XM_011536157.3:c.1010C>T, XM_011536157.2:c.1010C>T, XM_011536157.1:c.1010C>T, XM_011536154.3:c.1010C>T, XM_011536154.2:c.1010C>T, XM_011536154.1:c.1010C>T, XM_017011334.2:c.1010C>T, XM_017011334.1:c.1010C>T, XM_011536155.2:c.1010C>T, XM_011536155.1:c.1010C>T, XM_011536153.2:c.1010C>T, XM_011536153.1:c.1010C>T, XM_011536159.2:c.1010C>T, XM_011536159.1:c.1010C>T, XP_006715633.1:p.Ala337Val, NP_110411.1:p.Ala337Val, NP_001137429.1:p.Ala337Val, XP_011534459.1:p.Ala337Val, XP_011534456.1:p.Ala337Val, XP_016866823.1:p.Ala337Val, XP_011534457.1:p.Ala337Val, XP_011534455.1:p.Ala337Val, XP_011534461.1:p.Ala337Val

Select item 147226461413.

rs1472264614 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 6:96798836 (GRCh38)
6:97246712 (GRCh37)
Canonical SPDI:: NC_000006.12:96798835:G:T
Gene:: GPR63 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.96798836G>T, NC_000006.11:g.97246712G>T, XM_006715570.5:c.896C>A, XM_006715570.4:c.896C>A, XM_006715570.3:c.896C>A, XM_006715570.2:c.896C>A, XM_006715570.1:c.896C>A, NM_030784.4:c.896C>A, NM_030784.3:c.896C>A, NM_001143957.3:c.896C>A, NM_001143957.2:c.896C>A, XM_011536157.3:c.896C>A, XM_011536157.2:c.896C>A, XM_011536157.1:c.896C>A, XM_011536154.3:c.896C>A, XM_011536154.2:c.896C>A, XM_011536154.1:c.896C>A, XM_017011334.2:c.896C>A, XM_017011334.1:c.896C>A, XM_011536155.2:c.896C>A, XM_011536155.1:c.896C>A, XM_011536153.2:c.896C>A, XM_011536153.1:c.896C>A, XM_011536159.2:c.896C>A, XM_011536159.1:c.896C>A, XP_006715633.1:p.Pro299His, NP_110411.1:p.Pro299His, NP_001137429.1:p.Pro299His, XP_011534459.1:p.Pro299His, XP_011534456.1:p.Pro299His, XP_016866823.1:p.Pro299His, XP_011534457.1:p.Pro299His, XP_011534455.1:p.Pro299His, XP_011534461.1:p.Pro299His

Select item 146770175814.

rs1467701758 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:96799403 (GRCh38)
6:97247279 (GRCh37)
Canonical SPDI:: NC_000006.12:96799402:G:A
Gene:: GPR63 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (GnomAD_exomes)
A=0.000071/1 (TOMMO)
A=0.000342/1 (KOREAN)
HGVS:: NC_000006.12:g.96799403G>A, NC_000006.11:g.97247279G>A, XM_006715570.5:c.329C>T, XM_006715570.4:c.329C>T, XM_006715570.3:c.329C>T, XM_006715570.2:c.329C>T, XM_006715570.1:c.329C>T, NM_030784.4:c.329C>T, NM_030784.3:c.329C>T, NM_001143957.3:c.329C>T, NM_001143957.2:c.329C>T, XM_011536157.3:c.329C>T, XM_011536157.2:c.329C>T, XM_011536157.1:c.329C>T, XM_011536154.3:c.329C>T, XM_011536154.2:c.329C>T, XM_011536154.1:c.329C>T, XM_017011334.2:c.329C>T, XM_017011334.1:c.329C>T, XM_011536155.2:c.329C>T, XM_011536155.1:c.329C>T, XM_011536153.2:c.329C>T, XM_011536153.1:c.329C>T, XM_011536159.2:c.329C>T, XM_011536159.1:c.329C>T, XP_006715633.1:p.Ala110Val, NP_110411.1:p.Ala110Val, NP_001137429.1:p.Ala110Val, XP_011534459.1:p.Ala110Val, XP_011534456.1:p.Ala110Val, XP_016866823.1:p.Ala110Val, XP_011534457.1:p.Ala110Val, XP_011534455.1:p.Ala110Val, XP_011534461.1:p.Ala110Val

Select item 145832614515.

rs1458326145 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:96799148 (GRCh38)
6:97247024 (GRCh37)
Canonical SPDI:: NC_000006.12:96799147:G:A
Gene:: GPR63 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.96799148G>A, NC_000006.11:g.97247024G>A, XM_006715570.5:c.584C>T, XM_006715570.4:c.584C>T, XM_006715570.3:c.584C>T, XM_006715570.2:c.584C>T, XM_006715570.1:c.584C>T, NM_030784.4:c.584C>T, NM_030784.3:c.584C>T, NM_001143957.3:c.584C>T, NM_001143957.2:c.584C>T, XM_011536157.3:c.584C>T, XM_011536157.2:c.584C>T, XM_011536157.1:c.584C>T, XM_011536154.3:c.584C>T, XM_011536154.2:c.584C>T, XM_011536154.1:c.584C>T, XM_017011334.2:c.584C>T, XM_017011334.1:c.584C>T, XM_011536155.2:c.584C>T, XM_011536155.1:c.584C>T, XM_011536153.2:c.584C>T, XM_011536153.1:c.584C>T, XM_011536159.2:c.584C>T, XM_011536159.1:c.584C>T, XP_006715633.1:p.Ala195Val, NP_110411.1:p.Ala195Val, NP_001137429.1:p.Ala195Val, XP_011534459.1:p.Ala195Val, XP_011534456.1:p.Ala195Val, XP_016866823.1:p.Ala195Val, XP_011534457.1:p.Ala195Val, XP_011534455.1:p.Ala195Val, XP_011534461.1:p.Ala195Val

Select item 145565605416.

rs1455656054 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:96799136 (GRCh38)
6:97247012 (GRCh37)
Canonical SPDI:: NC_000006.12:96799135:A:G
Gene:: GPR63 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000006.12:g.96799136A>G, NC_000006.11:g.97247012A>G, XM_006715570.5:c.596T>C, XM_006715570.4:c.596T>C, XM_006715570.3:c.596T>C, XM_006715570.2:c.596T>C, XM_006715570.1:c.596T>C, NM_030784.4:c.596T>C, NM_030784.3:c.596T>C, NM_001143957.3:c.596T>C, NM_001143957.2:c.596T>C, XM_011536157.3:c.596T>C, XM_011536157.2:c.596T>C, XM_011536157.1:c.596T>C, XM_011536154.3:c.596T>C, XM_011536154.2:c.596T>C, XM_011536154.1:c.596T>C, XM_017011334.2:c.596T>C, XM_017011334.1:c.596T>C, XM_011536155.2:c.596T>C, XM_011536155.1:c.596T>C, XM_011536153.2:c.596T>C, XM_011536153.1:c.596T>C, XM_011536159.2:c.596T>C, XM_011536159.1:c.596T>C, XP_006715633.1:p.Ile199Thr, NP_110411.1:p.Ile199Thr, NP_001137429.1:p.Ile199Thr, XP_011534459.1:p.Ile199Thr, XP_011534456.1:p.Ile199Thr, XP_016866823.1:p.Ile199Thr, XP_011534457.1:p.Ile199Thr, XP_011534455.1:p.Ile199Thr, XP_011534461.1:p.Ile199Thr

Select item 145286906317.

rs1452869063 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:96798970 (GRCh38)
6:97246846 (GRCh37)
Canonical SPDI:: NC_000006.12:96798969:G:A
Gene:: GPR63 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (GnomAD_exomes)
A=0.000019/5 (TOPMED)
A=0.000035/1 (TOMMO)
A=0.000342/1 (KOREAN)
HGVS:: NC_000006.12:g.96798970G>A, NC_000006.11:g.97246846G>A, XM_006715570.5:c.762C>T, XM_006715570.4:c.762C>T, XM_006715570.3:c.762C>T, XM_006715570.2:c.762C>T, XM_006715570.1:c.762C>T, NM_030784.4:c.762C>T, NM_030784.3:c.762C>T, NM_001143957.3:c.762C>T, NM_001143957.2:c.762C>T, XM_011536157.3:c.762C>T, XM_011536157.2:c.762C>T, XM_011536157.1:c.762C>T, XM_011536154.3:c.762C>T, XM_011536154.2:c.762C>T, XM_011536154.1:c.762C>T, XM_017011334.2:c.762C>T, XM_017011334.1:c.762C>T, XM_011536155.2:c.762C>T, XM_011536155.1:c.762C>T, XM_011536153.2:c.762C>T, XM_011536153.1:c.762C>T, XM_011536159.2:c.762C>T, XM_011536159.1:c.762C>T

Select item 145112436418.

rs1451124364 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:96799221 (GRCh38)
6:97247097 (GRCh37)
Canonical SPDI:: NC_000006.12:96799220:T:C
Gene:: GPR63 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.96799221T>C, NC_000006.11:g.97247097T>C, XM_006715570.5:c.511A>G, XM_006715570.4:c.511A>G, XM_006715570.3:c.511A>G, XM_006715570.2:c.511A>G, XM_006715570.1:c.511A>G, NM_030784.4:c.511A>G, NM_030784.3:c.511A>G, NM_001143957.3:c.511A>G, NM_001143957.2:c.511A>G, XM_011536157.3:c.511A>G, XM_011536157.2:c.511A>G, XM_011536157.1:c.511A>G, XM_011536154.3:c.511A>G, XM_011536154.2:c.511A>G, XM_011536154.1:c.511A>G, XM_017011334.2:c.511A>G, XM_017011334.1:c.511A>G, XM_011536155.2:c.511A>G, XM_011536155.1:c.511A>G, XM_011536153.2:c.511A>G, XM_011536153.1:c.511A>G, XM_011536159.2:c.511A>G, XM_011536159.1:c.511A>G, XP_006715633.1:p.Ile171Val, NP_110411.1:p.Ile171Val, NP_001137429.1:p.Ile171Val, XP_011534459.1:p.Ile171Val, XP_011534456.1:p.Ile171Val, XP_016866823.1:p.Ile171Val, XP_011534457.1:p.Ile171Val, XP_011534455.1:p.Ile171Val, XP_011534461.1:p.Ile171Val

Select item 144962345019.

rs1449623450 [Homo sapiens]

Variant type:: DEL
Alleles:: G>- [Show Flanks]
Chromosome:: 6:96798622 (GRCh38)
6:97246498 (GRCh37)
Canonical SPDI:: NC_000006.12:96798621:G:
Gene:: GPR63 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency
MAF:: -=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.96798622del, NC_000006.11:g.97246498del, XM_006715570.5:c.1110del, XM_006715570.4:c.1110del, XM_006715570.3:c.1110del, XM_006715570.2:c.1110del, XM_006715570.1:c.1110del, NM_030784.4:c.1110del, NM_030784.3:c.1110del, NM_001143957.3:c.1110del, NM_001143957.2:c.1110del, XM_011536157.3:c.1110del, XM_011536157.2:c.1110del, XM_011536157.1:c.1110del, XM_011536154.3:c.1110del, XM_011536154.2:c.1110del, XM_011536154.1:c.1110del, XM_017011334.2:c.1110del, XM_017011334.1:c.1110del, XM_011536155.2:c.1110del, XM_011536155.1:c.1110del, XM_011536153.2:c.1110del, XM_011536153.1:c.1110del, XM_011536159.2:c.1110del, XM_011536159.1:c.1110del, XP_006715633.1:p.Tyr371fs, NP_110411.1:p.Tyr371fs, NP_001137429.1:p.Tyr371fs, XP_011534459.1:p.Tyr371fs, XP_011534456.1:p.Tyr371fs, XP_016866823.1:p.Tyr371fs, XP_011534457.1:p.Tyr371fs, XP_011534455.1:p.Tyr371fs, XP_011534461.1:p.Tyr371fs

Select item 144674160820.

rs1446741608 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 6:96798533 (GRCh38)
6:97246409 (GRCh37)
Canonical SPDI:: NC_000006.12:96798532:G:C
Gene:: GPR63 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000006.12:g.96798533G>C, NC_000006.11:g.97246409G>C, XM_006715570.5:c.1199C>G, XM_006715570.4:c.1199C>G, XM_006715570.3:c.1199C>G, XM_006715570.2:c.1199C>G, XM_006715570.1:c.1199C>G, NM_030784.4:c.1199C>G, NM_030784.3:c.1199C>G, NM_001143957.3:c.1199C>G, NM_001143957.2:c.1199C>G, XM_011536157.3:c.1199C>G, XM_011536157.2:c.1199C>G, XM_011536157.1:c.1199C>G, XM_011536154.3:c.1199C>G, XM_011536154.2:c.1199C>G, XM_011536154.1:c.1199C>G, XM_017011334.2:c.1199C>G, XM_017011334.1:c.1199C>G, XM_011536155.2:c.1199C>G, XM_011536155.1:c.1199C>G, XM_011536153.2:c.1199C>G, XM_011536153.1:c.1199C>G, XM_011536159.2:c.1199C>G, XM_011536159.1:c.1199C>G, XP_006715633.1:p.Thr400Arg, NP_110411.1:p.Thr400Arg, NP_001137429.1:p.Thr400Arg, XP_011534459.1:p.Thr400Arg, XP_011534456.1:p.Thr400Arg, XP_016866823.1:p.Thr400Arg, XP_011534457.1:p.Thr400Arg, XP_011534455.1:p.Thr400Arg, XP_011534461.1:p.Thr400Arg

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