SNP Links for Protein (Select 1162503566) - SNP

Select item 14890237721.

rs1489023772 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:168104559 (GRCh38)
1:168073797 (GRCh37)
Canonical SPDI:: NC_000001.11:168104558:C:T
Gene:: GPR161 (Varview)
Functional Consequence:: intron_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.168104559C>T, NC_000001.10:g.168073797C>T, NG_053052.1:g.38109G>A, NM_153832.3:c.292G>A, NM_153832.2:c.292G>A, NM_001267610.2:c.292G>A, NM_001267610.1:c.292G>A, NM_001375885.1:c.292G>A, NM_001349632.1:c.292G>A, NM_001375884.1:c.292G>A, NM_001267609.1:c.352G>A, NM_001349633.1:c.292G>A, NM_001349634.1:c.292G>A, NM_001381909.1:c.292G>A, NM_001375883.1:c.292G>A, NM_001267611.1:c.343G>A, NM_007369.2:c.292G>A, NM_007369.1:c.292G>A, NP_722561.1:p.Val98Met, NP_001254539.1:p.Val98Met, NP_001362814.1:p.Val98Met, NP_001336561.1:p.Val98Met, NP_001362813.1:p.Val98Met, NP_001254538.1:p.Val118Met, NP_001336562.1:p.Val98Met, NP_001336563.1:p.Val98Met, NP_001368838.1:p.Val98Met, NP_001362812.1:p.Val98Met, NP_001254540.1:p.Val115Met

Select item 14867719142.

rs1486771914 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:168097090 (GRCh38)
1:168066328 (GRCh37)
Canonical SPDI:: NC_000001.11:168097089:C:T
Gene:: GPR161 (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=0.000035/1 (TOMMO)
HGVS:: NC_000001.11:g.168097090C>T, NC_000001.10:g.168066328C>T, NG_053052.1:g.45578G>A, NM_153832.3:c.517G>A, NM_153832.2:c.517G>A, NM_001267612.2:c.121G>A, NM_001267612.1:c.121G>A, NM_001267610.2:c.517G>A, NM_001267610.1:c.517G>A, NM_001375885.1:c.517G>A, NM_001349632.1:c.517G>A, NM_001375884.1:c.517G>A, NM_001267609.1:c.577G>A, NM_001349633.1:c.517G>A, NM_001349634.1:c.517G>A, NM_001381909.1:c.517G>A, NM_001375883.1:c.517G>A, NM_001267611.1:c.568G>A, NM_001349635.1:c.121G>A, NM_001267613.1:c.283G>A, NM_001267614.1:c.175G>A, NM_007369.2:c.517G>A, NM_007369.1:c.517G>A, NP_722561.1:p.Glu173Lys, NP_001254541.1:p.Glu41Lys, NP_001254539.1:p.Glu173Lys, NP_001362814.1:p.Glu173Lys, NP_001336561.1:p.Glu173Lys, NP_001362813.1:p.Glu173Lys, NP_001254538.1:p.Glu193Lys, NP_001336562.1:p.Glu173Lys, NP_001336563.1:p.Glu173Lys, NP_001368838.1:p.Glu173Lys, NP_001362812.1:p.Glu173Lys, NP_001254540.1:p.Glu190Lys, NP_001336564.1:p.Glu41Lys, NP_001254542.1:p.Glu95Lys, NP_001254543.1:p.Glu59Lys

Select item 14857926283.

rs1485792628 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:168104591 (GRCh38)
1:168073829 (GRCh37)
Canonical SPDI:: NC_000001.11:168104590:C:T
Gene:: GPR161 (Varview)
Functional Consequence:: intron_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: T=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.168104591C>T, NC_000001.10:g.168073829C>T, NG_053052.1:g.38077G>A, NM_153832.3:c.260G>A, NM_153832.2:c.260G>A, NM_001267610.2:c.260G>A, NM_001267610.1:c.260G>A, NM_001375885.1:c.260G>A, NM_001349632.1:c.260G>A, NM_001375884.1:c.260G>A, NM_001267609.1:c.320G>A, NM_001349633.1:c.260G>A, NM_001349634.1:c.260G>A, NM_001381909.1:c.260G>A, NM_001375883.1:c.260G>A, NM_001267611.1:c.311G>A, NM_007369.2:c.260G>A, NM_007369.1:c.260G>A, NP_722561.1:p.Ser87Asn, NP_001254539.1:p.Ser87Asn, NP_001362814.1:p.Ser87Asn, NP_001336561.1:p.Ser87Asn, NP_001362813.1:p.Ser87Asn, NP_001254538.1:p.Ser107Asn, NP_001336562.1:p.Ser87Asn, NP_001336563.1:p.Ser87Asn, NP_001368838.1:p.Ser87Asn, NP_001362812.1:p.Ser87Asn, NP_001254540.1:p.Ser104Asn

Select item 14784453684.

rs1478445368 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:168087681 (GRCh38)
1:168056919 (GRCh37)
Canonical SPDI:: NC_000001.11:168087680:C:T
Gene:: GPR161 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.168087681C>T, NC_000001.10:g.168056919C>T, NG_053052.1:g.54987G>A, NM_153832.3:c.1228G>A, NM_153832.2:c.1228G>A, NM_001267612.2:c.832G>A, NM_001267612.1:c.832G>A, NM_001267610.2:c.1228G>A, NM_001267610.1:c.1228G>A, NM_001375885.1:c.1228G>A, NM_001349632.1:c.1228G>A, NM_001375884.1:c.1228G>A, NM_001267609.1:c.1288G>A, NM_001349633.1:c.1228G>A, NM_001349634.1:c.1228G>A, NM_001381909.1:c.1228G>A, NM_001375883.1:c.1228G>A, NM_001267611.1:c.1279G>A, NM_001349635.1:c.832G>A, NM_001267613.1:c.994G>A, NM_001267614.1:c.886G>A, NP_722561.1:p.Asp410Asn, NP_001254541.1:p.Asp278Asn, NP_001254539.1:p.Asp410Asn, NP_001362814.1:p.Asp410Asn, NP_001336561.1:p.Asp410Asn, NP_001362813.1:p.Asp410Asn, NP_001254538.1:p.Asp430Asn, NP_001336562.1:p.Asp410Asn, NP_001336563.1:p.Asp410Asn, NP_001368838.1:p.Asp410Asn, NP_001362812.1:p.Asp410Asn, NP_001254540.1:p.Asp427Asn, NP_001336564.1:p.Asp278Asn, NP_001254542.1:p.Asp332Asn, NP_001254543.1:p.Asp296Asn

Select item 14762036995.

rs1476203699 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:168085622 (GRCh38)
1:168054860 (GRCh37)
Canonical SPDI:: NC_000001.11:168085621:C:G
Gene:: GPR161 (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=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.168085622C>G, NC_000001.10:g.168054860C>G, NG_053052.1:g.57046G>C, NM_153832.3:c.1499G>C, NM_153832.2:c.1499G>C, NM_001267612.2:c.1103G>C, NM_001267612.1:c.1103G>C, NM_001267610.2:c.1499G>C, NM_001267610.1:c.1499G>C, NM_001375885.1:c.1499G>C, NM_001349632.1:c.1499G>C, NM_001375884.1:c.1499G>C, NM_001267609.1:c.1559G>C, NM_001349633.1:c.1499G>C, NM_001349634.1:c.1499G>C, NM_001381909.1:c.1499G>C, NM_001375883.1:c.1499G>C, NM_001267611.1:c.1550G>C, NM_001349635.1:c.1103G>C, NM_001267613.1:c.1265G>C, NM_001267614.1:c.1157G>C, NP_722561.1:p.Gly500Ala, NP_001254541.1:p.Gly368Ala, NP_001254539.1:p.Gly500Ala, NP_001362814.1:p.Gly500Ala, NP_001336561.1:p.Gly500Ala, NP_001362813.1:p.Gly500Ala, NP_001254538.1:p.Gly520Ala, NP_001336562.1:p.Gly500Ala, NP_001336563.1:p.Gly500Ala, NP_001368838.1:p.Gly500Ala, NP_001362812.1:p.Gly500Ala, NP_001254540.1:p.Gly517Ala, NP_001336564.1:p.Gly368Ala, NP_001254542.1:p.Gly422Ala, NP_001254543.1:p.Gly386Ala

Select item 14759263356.

rs1475926335 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:168104569 (GRCh38)
1:168073807 (GRCh37)
Canonical SPDI:: NC_000001.11:168104568:G:A
Gene:: GPR161 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.168104569G>A, NC_000001.10:g.168073807G>A, NG_053052.1:g.38099C>T, NM_153832.3:c.282C>T, NM_153832.2:c.282C>T, NM_001267610.2:c.282C>T, NM_001267610.1:c.282C>T, NM_001375885.1:c.282C>T, NM_001349632.1:c.282C>T, NM_001375884.1:c.282C>T, NM_001267609.1:c.342C>T, NM_001349633.1:c.282C>T, NM_001349634.1:c.282C>T, NM_001381909.1:c.282C>T, NM_001375883.1:c.282C>T, NM_001267611.1:c.333C>T, NM_007369.2:c.282C>T, NM_007369.1:c.282C>T

Select item 14721142207.

rs1472114220 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:168096698 (GRCh38)
1:168065936 (GRCh37)
Canonical SPDI:: NC_000001.11:168096697:C:T
Gene:: GPR161 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0./0 (GnomAD)
T=0.000008/2 (GnomAD_exomes)
T=0.000035/1 (TOMMO)
HGVS:: NC_000001.11:g.168096698C>T, NC_000001.10:g.168065936C>T, NG_053052.1:g.45970G>A, NM_153832.3:c.909G>A, NM_153832.2:c.909G>A, NM_001267612.2:c.513G>A, NM_001267612.1:c.513G>A, NM_001267610.2:c.909G>A, NM_001267610.1:c.909G>A, NM_001375885.1:c.909G>A, NM_001349632.1:c.909G>A, NM_001375884.1:c.909G>A, NM_001267609.1:c.969G>A, NM_001349633.1:c.909G>A, NM_001349634.1:c.909G>A, NM_001381909.1:c.909G>A, NM_001375883.1:c.909G>A, NM_001267611.1:c.960G>A, NM_001349635.1:c.513G>A, NM_001267613.1:c.675G>A, NM_001267614.1:c.567G>A, NM_007369.2:c.909G>A, NM_007369.1:c.909G>A

Select item 14719254968.

rs1471925496 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:168096935 (GRCh38)
1:168066173 (GRCh37)
Canonical SPDI:: NC_000001.11:168096934:A:G
Gene:: GPR161 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.168096935A>G, NC_000001.10:g.168066173A>G, NG_053052.1:g.45733T>C, NM_153832.3:c.672T>C, NM_153832.2:c.672T>C, NM_001267612.2:c.276T>C, NM_001267612.1:c.276T>C, NM_001267610.2:c.672T>C, NM_001267610.1:c.672T>C, NM_001375885.1:c.672T>C, NM_001349632.1:c.672T>C, NM_001375884.1:c.672T>C, NM_001267609.1:c.732T>C, NM_001349633.1:c.672T>C, NM_001349634.1:c.672T>C, NM_001381909.1:c.672T>C, NM_001375883.1:c.672T>C, NM_001267611.1:c.723T>C, NM_001349635.1:c.276T>C, NM_001267613.1:c.438T>C, NM_001267614.1:c.330T>C, NM_007369.2:c.672T>C, NM_007369.1:c.672T>C

Select item 14670718719.

rs1467071871 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:168104693 (GRCh38)
1:168073931 (GRCh37)
Canonical SPDI:: NC_000001.11:168104692:T:C
Gene:: GPR161 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.168104693T>C, NC_000001.10:g.168073931T>C, NG_053052.1:g.37975A>G, NM_153832.3:c.158A>G, NM_153832.2:c.158A>G, NM_001267610.2:c.158A>G, NM_001267610.1:c.158A>G, NM_001375885.1:c.158A>G, NM_001349632.1:c.158A>G, NM_001375884.1:c.158A>G, NM_001267609.1:c.218A>G, NM_001349633.1:c.158A>G, NM_001349634.1:c.158A>G, NM_001381909.1:c.158A>G, NM_001375883.1:c.158A>G, NM_001267611.1:c.209A>G, NM_007369.2:c.158A>G, NM_007369.1:c.158A>G, NP_722561.1:p.Tyr53Cys, NP_001254539.1:p.Tyr53Cys, NP_001362814.1:p.Tyr53Cys, NP_001336561.1:p.Tyr53Cys, NP_001362813.1:p.Tyr53Cys, NP_001254538.1:p.Tyr73Cys, NP_001336562.1:p.Tyr53Cys, NP_001336563.1:p.Tyr53Cys, NP_001368838.1:p.Tyr53Cys, NP_001362812.1:p.Tyr53Cys, NP_001254540.1:p.Tyr70Cys

Select item 146597468010.

rs1465974680 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 1:168090636 (GRCh38)
1:168059874 (GRCh37)
Canonical SPDI:: NC_000001.11:168090635:T:A
Gene:: GPR161 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000001.11:g.168090636T>A, NC_000001.10:g.168059874T>A, NG_053052.1:g.52032A>T, NM_153832.3:c.1132A>T, NM_153832.2:c.1132A>T, NM_001267612.2:c.736A>T, NM_001267612.1:c.736A>T, NM_001267610.2:c.1132A>T, NM_001267610.1:c.1132A>T, NM_001375885.1:c.1132A>T, NM_001349632.1:c.1132A>T, NM_001375884.1:c.1132A>T, NM_001267609.1:c.1192A>T, NM_001349633.1:c.1132A>T, NM_001349634.1:c.1132A>T, NM_001381909.1:c.1132A>T, NM_001375883.1:c.1132A>T, NM_001267611.1:c.1183A>T, NM_001349635.1:c.736A>T, NM_001267613.1:c.898A>T, NM_001267614.1:c.790A>T, NM_007369.2:c.1132A>T, NM_007369.1:c.1132A>T, NP_722561.1:p.Met378Leu, NP_001254541.1:p.Met246Leu, NP_001254539.1:p.Met378Leu, NP_001362814.1:p.Met378Leu, NP_001336561.1:p.Met378Leu, NP_001362813.1:p.Met378Leu, NP_001254538.1:p.Met398Leu, NP_001336562.1:p.Met378Leu, NP_001336563.1:p.Met378Leu, NP_001368838.1:p.Met378Leu, NP_001362812.1:p.Met378Leu, NP_001254540.1:p.Met395Leu, NP_001336564.1:p.Met246Leu, NP_001254542.1:p.Met300Leu, NP_001254543.1:p.Met264Leu

Select item 146392278411.

rs1463922784 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:168097157 (GRCh38)
1:168066395 (GRCh37)
Canonical SPDI:: NC_000001.11:168097156:G:A
Gene:: GPR161 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000142/2 (ALFA)
A=0.000011/3 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.168097157G>A, NC_000001.10:g.168066395G>A, NG_053052.1:g.45511C>T, NM_153832.3:c.450C>T, NM_153832.2:c.450C>T, NM_001267612.2:c.54C>T, NM_001267612.1:c.54C>T, NM_001267610.2:c.450C>T, NM_001267610.1:c.450C>T, NM_001375885.1:c.450C>T, NM_001349632.1:c.450C>T, NM_001375884.1:c.450C>T, NM_001267609.1:c.510C>T, NM_001349633.1:c.450C>T, NM_001349634.1:c.450C>T, NM_001381909.1:c.450C>T, NM_001375883.1:c.450C>T, NM_001267611.1:c.501C>T, NM_001349635.1:c.54C>T, NM_001267613.1:c.216C>T, NM_001267614.1:c.108C>T, NM_007369.2:c.450C>T, NM_007369.1:c.450C>T

Select item 145826178512.

rs1458261785 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:168096551 (GRCh38)
1:168065789 (GRCh37)
Canonical SPDI:: NC_000001.11:168096550:T:C
Gene:: GPR161 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.168096551T>C, NC_000001.10:g.168065789T>C, NG_053052.1:g.46117A>G, NM_153832.3:c.1056A>G, NM_153832.2:c.1056A>G, NM_001267612.2:c.660A>G, NM_001267612.1:c.660A>G, NM_001267610.2:c.1056A>G, NM_001267610.1:c.1056A>G, NM_001375885.1:c.1056A>G, NM_001349632.1:c.1056A>G, NM_001375884.1:c.1056A>G, NM_001267609.1:c.1116A>G, NM_001349633.1:c.1056A>G, NM_001349634.1:c.1056A>G, NM_001381909.1:c.1056A>G, NM_001375883.1:c.1056A>G, NM_001267611.1:c.1107A>G, NM_001349635.1:c.660A>G, NM_001267613.1:c.822A>G, NM_001267614.1:c.714A>G, NM_007369.2:c.1056A>G, NM_007369.1:c.1056A>G

Select item 145479923513.

rs1454799235 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:168096767 (GRCh38)
1:168066005 (GRCh37)
Canonical SPDI:: NC_000001.11:168096766:C:T
Gene:: GPR161 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.168096767C>T, NC_000001.10:g.168066005C>T, NG_053052.1:g.45901G>A, NM_153832.3:c.840G>A, NM_153832.2:c.840G>A, NM_001267612.2:c.444G>A, NM_001267612.1:c.444G>A, NM_001267610.2:c.840G>A, NM_001267610.1:c.840G>A, NM_001375885.1:c.840G>A, NM_001349632.1:c.840G>A, NM_001375884.1:c.840G>A, NM_001267609.1:c.900G>A, NM_001349633.1:c.840G>A, NM_001349634.1:c.840G>A, NM_001381909.1:c.840G>A, NM_001375883.1:c.840G>A, NM_001267611.1:c.891G>A, NM_001349635.1:c.444G>A, NM_001267613.1:c.606G>A, NM_001267614.1:c.498G>A, NM_007369.2:c.840G>A, NM_007369.1:c.840G>A, NP_722561.1:p.Met280Ile, NP_001254541.1:p.Met148Ile, NP_001254539.1:p.Met280Ile, NP_001362814.1:p.Met280Ile, NP_001336561.1:p.Met280Ile, NP_001362813.1:p.Met280Ile, NP_001254538.1:p.Met300Ile, NP_001336562.1:p.Met280Ile, NP_001336563.1:p.Met280Ile, NP_001368838.1:p.Met280Ile, NP_001362812.1:p.Met280Ile, NP_001254540.1:p.Met297Ile, NP_001336564.1:p.Met148Ile, NP_001254542.1:p.Met202Ile, NP_001254543.1:p.Met166Ile

Select item 145475437114.

rs1454754371 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:168097014 (GRCh38)
1:168066252 (GRCh37)
Canonical SPDI:: NC_000001.11:168097013:A:G
Gene:: GPR161 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.168097014A>G, NC_000001.10:g.168066252A>G, NG_053052.1:g.45654T>C, NM_153832.3:c.593T>C, NM_153832.2:c.593T>C, NM_001267612.2:c.197T>C, NM_001267612.1:c.197T>C, NM_001267610.2:c.593T>C, NM_001267610.1:c.593T>C, NM_001375885.1:c.593T>C, NM_001349632.1:c.593T>C, NM_001375884.1:c.593T>C, NM_001267609.1:c.653T>C, NM_001349633.1:c.593T>C, NM_001349634.1:c.593T>C, NM_001381909.1:c.593T>C, NM_001375883.1:c.593T>C, NM_001267611.1:c.644T>C, NM_001349635.1:c.197T>C, NM_001267613.1:c.359T>C, NM_001267614.1:c.251T>C, NM_007369.2:c.593T>C, NM_007369.1:c.593T>C, NP_722561.1:p.Leu198Pro, NP_001254541.1:p.Leu66Pro, NP_001254539.1:p.Leu198Pro, NP_001362814.1:p.Leu198Pro, NP_001336561.1:p.Leu198Pro, NP_001362813.1:p.Leu198Pro, NP_001254538.1:p.Leu218Pro, NP_001336562.1:p.Leu198Pro, NP_001336563.1:p.Leu198Pro, NP_001368838.1:p.Leu198Pro, NP_001362812.1:p.Leu198Pro, NP_001254540.1:p.Leu215Pro, NP_001336564.1:p.Leu66Pro, NP_001254542.1:p.Leu120Pro, NP_001254543.1:p.Leu84Pro

Select item 145402288615.

rs1454022886 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:168090660 (GRCh38)
1:168059898 (GRCh37)
Canonical SPDI:: NC_000001.11:168090659:G:A
Gene:: GPR161 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.168090660G>A, NC_000001.10:g.168059898G>A, NG_053052.1:g.52008C>T, NM_153832.3:c.1108C>T, NM_153832.2:c.1108C>T, NM_001267612.2:c.712C>T, NM_001267612.1:c.712C>T, NM_001267610.2:c.1108C>T, NM_001267610.1:c.1108C>T, NM_001375885.1:c.1108C>T, NM_001349632.1:c.1108C>T, NM_001375884.1:c.1108C>T, NM_001267609.1:c.1168C>T, NM_001349633.1:c.1108C>T, NM_001349634.1:c.1108C>T, NM_001381909.1:c.1108C>T, NM_001375883.1:c.1108C>T, NM_001267611.1:c.1159C>T, NM_001349635.1:c.712C>T, NM_001267613.1:c.874C>T, NM_001267614.1:c.766C>T, NM_007369.2:c.1108C>T, NM_007369.1:c.1108C>T

Select item 145191731816.

rs1451917318 [Homo sapiens]

Variant type:: DEL
Alleles:: T>- [Show Flanks]
Chromosome:: 1:168097098 (GRCh38)
1:168066336 (GRCh37)
Canonical SPDI:: NC_000001.11:168097097:T:
Gene:: GPR161 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.168097098del, NC_000001.10:g.168066336del, NG_053052.1:g.45570del, NM_153832.3:c.509del, NM_153832.2:c.509del, NM_001267612.2:c.113del, NM_001267612.1:c.113del, NM_001267610.2:c.509del, NM_001267610.1:c.509del, NM_001375885.1:c.509del, NM_001349632.1:c.509del, NM_001375884.1:c.509del, NM_001267609.1:c.569del, NM_001349633.1:c.509del, NM_001349634.1:c.509del, NM_001381909.1:c.509del, NM_001375883.1:c.509del, NM_001267611.1:c.560del, NM_001349635.1:c.113del, NM_001267613.1:c.275del, NM_001267614.1:c.167del, NM_007369.2:c.509del, NM_007369.1:c.509del, NP_722561.1:p.Glu170fs, NP_001254541.1:p.Glu38fs, NP_001254539.1:p.Glu170fs, NP_001362814.1:p.Glu170fs, NP_001336561.1:p.Glu170fs, NP_001362813.1:p.Glu170fs, NP_001254538.1:p.Glu190fs, NP_001336562.1:p.Glu170fs, NP_001336563.1:p.Glu170fs, NP_001368838.1:p.Glu170fs, NP_001362812.1:p.Glu170fs, NP_001254540.1:p.Glu187fs, NP_001336564.1:p.Glu38fs, NP_001254542.1:p.Glu92fs, NP_001254543.1:p.Glu56fs

Select item 144820196217.

rs1448201962 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:168096518 (GRCh38)
1:168065756 (GRCh37)
Canonical SPDI:: NC_000001.11:168096517:G:A
Gene:: GPR161 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000012/3 (GnomAD_exomes)
HGVS:: NC_000001.11:g.168096518G>A, NC_000001.10:g.168065756G>A, NG_053052.1:g.46150C>T, NM_153832.3:c.1089C>T, NM_153832.2:c.1089C>T, NM_001267612.2:c.693C>T, NM_001267612.1:c.693C>T, NM_001267610.2:c.1089C>T, NM_001267610.1:c.1089C>T, NM_001375885.1:c.1089C>T, NM_001349632.1:c.1089C>T, NM_001375884.1:c.1089C>T, NM_001267609.1:c.1149C>T, NM_001349633.1:c.1089C>T, NM_001349634.1:c.1089C>T, NM_001381909.1:c.1089C>T, NM_001375883.1:c.1089C>T, NM_001267611.1:c.1140C>T, NM_001349635.1:c.693C>T, NM_001267613.1:c.855C>T, NM_001267614.1:c.747C>T, NM_007369.2:c.1089C>T, NM_007369.1:c.1089C>T

Select item 144454677618.

rs1444546776 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:168085595 (GRCh38)
1:168054833 (GRCh37)
Canonical SPDI:: NC_000001.11:168085594:A:G
Gene:: GPR161 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000001.11:g.168085595A>G, NC_000001.10:g.168054833A>G, NG_053052.1:g.57073T>C, NM_153832.3:c.1526T>C, NM_153832.2:c.1526T>C, NM_001267612.2:c.1130T>C, NM_001267612.1:c.1130T>C, NM_001267610.2:c.1526T>C, NM_001267610.1:c.1526T>C, NM_001375885.1:c.1526T>C, NM_001349632.1:c.1526T>C, NM_001375884.1:c.1526T>C, NM_001267609.1:c.1586T>C, NM_001349633.1:c.1526T>C, NM_001349634.1:c.1526T>C, NM_001381909.1:c.1526T>C, NM_001375883.1:c.1526T>C, NM_001267611.1:c.1577T>C, NM_001349635.1:c.1130T>C, NM_001267613.1:c.1292T>C, NM_001267614.1:c.1184T>C, NP_722561.1:p.Val509Ala, NP_001254541.1:p.Val377Ala, NP_001254539.1:p.Val509Ala, NP_001362814.1:p.Val509Ala, NP_001336561.1:p.Val509Ala, NP_001362813.1:p.Val509Ala, NP_001254538.1:p.Val529Ala, NP_001336562.1:p.Val509Ala, NP_001336563.1:p.Val509Ala, NP_001368838.1:p.Val509Ala, NP_001362812.1:p.Val509Ala, NP_001254540.1:p.Val526Ala, NP_001336564.1:p.Val377Ala, NP_001254542.1:p.Val431Ala, NP_001254543.1:p.Val395Ala

Select item 144214990919.

rs1442149909 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:168104654 (GRCh38)
1:168073892 (GRCh37)
Canonical SPDI:: NC_000001.11:168104653:A:G
Gene:: GPR161 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.168104654A>G, NC_000001.10:g.168073892A>G, NG_053052.1:g.38014T>C, NM_153832.3:c.197T>C, NM_153832.2:c.197T>C, NM_001267610.2:c.197T>C, NM_001267610.1:c.197T>C, NM_001375885.1:c.197T>C, NM_001349632.1:c.197T>C, NM_001375884.1:c.197T>C, NM_001267609.1:c.257T>C, NM_001349633.1:c.197T>C, NM_001349634.1:c.197T>C, NM_001381909.1:c.197T>C, NM_001375883.1:c.197T>C, NM_001267611.1:c.248T>C, NM_007369.2:c.197T>C, NM_007369.1:c.197T>C, NP_722561.1:p.Val66Ala, NP_001254539.1:p.Val66Ala, NP_001362814.1:p.Val66Ala, NP_001336561.1:p.Val66Ala, NP_001362813.1:p.Val66Ala, NP_001254538.1:p.Val86Ala, NP_001336562.1:p.Val66Ala, NP_001336563.1:p.Val66Ala, NP_001368838.1:p.Val66Ala, NP_001362812.1:p.Val66Ala, NP_001254540.1:p.Val83Ala

Select item 144091280420.

rs1440912804 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 1:168096988 (GRCh38)
1:168066226 (GRCh37)
Canonical SPDI:: NC_000001.11:168096987:A:C
Gene:: GPR161 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.168096988A>C, NC_000001.10:g.168066226A>C, NG_053052.1:g.45680T>G, NM_153832.3:c.619T>G, NM_153832.2:c.619T>G, NM_001267612.2:c.223T>G, NM_001267612.1:c.223T>G, NM_001267610.2:c.619T>G, NM_001267610.1:c.619T>G, NM_001375885.1:c.619T>G, NM_001349632.1:c.619T>G, NM_001375884.1:c.619T>G, NM_001267609.1:c.679T>G, NM_001349633.1:c.619T>G, NM_001349634.1:c.619T>G, NM_001381909.1:c.619T>G, NM_001375883.1:c.619T>G, NM_001267611.1:c.670T>G, NM_001349635.1:c.223T>G, NM_001267613.1:c.385T>G, NM_001267614.1:c.277T>G, NM_007369.2:c.619T>G, NM_007369.1:c.619T>G, NP_722561.1:p.Cys207Gly, NP_001254541.1:p.Cys75Gly, NP_001254539.1:p.Cys207Gly, NP_001362814.1:p.Cys207Gly, NP_001336561.1:p.Cys207Gly, NP_001362813.1:p.Cys207Gly, NP_001254538.1:p.Cys227Gly, NP_001336562.1:p.Cys207Gly, NP_001336563.1:p.Cys207Gly, NP_001368838.1:p.Cys207Gly, NP_001362812.1:p.Cys207Gly, NP_001254540.1:p.Cys224Gly, NP_001336564.1:p.Cys75Gly, NP_001254542.1:p.Cys129Gly, NP_001254543.1:p.Cys93Gly

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Result Filters

Clinical Significance

Validation Status

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Global MAF

Custom range

Additional filters

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Items: 1 to 20 of 547

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