SNP Links for Protein (Select 1023300861) - SNP

Links from Protein

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Select item 14868447131.

rs1486844713 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:78961497 (GRCh38)
X:78216994 (GRCh37)
Canonical SPDI:: NC_000023.11:78961496:C:T
Gene:: P2RY10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.78961497C>T, NC_000023.10:g.78216994C>T, NG_013276.2:g.21166C>T, NM_014499.4:c.977C>T, NM_014499.3:c.977C>T, NM_014499.2:c.977C>T, NM_198333.3:c.977C>T, NM_198333.2:c.977C>T, NM_198333.1:c.977C>T, NM_001324218.2:c.977C>T, NM_001324218.1:c.977C>T, NM_001324225.2:c.1052C>T, NM_001324225.1:c.1052C>T, NM_001324221.2:c.1028C>T, NM_001324221.1:c.1028C>T, XM_047441998.1:c.977C>T, NP_055314.1:p.Ser326Phe, NP_938147.1:p.Ser326Phe, NP_001311147.1:p.Ser326Phe, NP_001311154.1:p.Ser351Phe, NP_001311150.1:p.Ser343Phe, XP_047297954.1:p.Ser326Phe

Select item 14787122062.

rs1478712206 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:78960727 (GRCh38)
X:78216224 (GRCh37)
Canonical SPDI:: NC_000023.11:78960726:C:T
Gene:: P2RY10 (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_000023.11:g.78960727C>T, NC_000023.10:g.78216224C>T, NG_013276.2:g.20396C>T, NM_014499.4:c.207C>T, NM_014499.3:c.207C>T, NM_014499.2:c.207C>T, NM_198333.3:c.207C>T, NM_198333.2:c.207C>T, NM_198333.1:c.207C>T, NM_001324218.2:c.207C>T, NM_001324218.1:c.207C>T, NM_001324225.2:c.282C>T, NM_001324225.1:c.282C>T, NM_001324221.2:c.258C>T, NM_001324221.1:c.258C>T, XM_047441998.1:c.207C>T

Select item 14760640543.

rs1476064054 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: X:78960577 (GRCh38)
X:78216074 (GRCh37)
Canonical SPDI:: NC_000023.11:78960576:C:A
Gene:: P2RY10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.78960577C>A, NC_000023.10:g.78216074C>A, NG_013276.2:g.20246C>A, NM_014499.4:c.57C>A, NM_014499.3:c.57C>A, NM_014499.2:c.57C>A, NM_198333.3:c.57C>A, NM_198333.2:c.57C>A, NM_198333.1:c.57C>A, NM_001324218.2:c.57C>A, NM_001324218.1:c.57C>A, NM_001324225.2:c.132C>A, NM_001324225.1:c.132C>A, NM_001324221.2:c.108C>A, NM_001324221.1:c.108C>A, XM_047441998.1:c.57C>A, NP_055314.1:p.Ser19Arg, NP_938147.1:p.Ser19Arg, NP_001311147.1:p.Ser19Arg, NP_001311154.1:p.Ser44Arg, NP_001311150.1:p.Ser36Arg, XP_047297954.1:p.Ser19Arg

Select item 14703456424.

rs1470345642 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:78961494 (GRCh38)
X:78216991 (GRCh37)
Canonical SPDI:: NC_000023.11:78961493:G:A
Gene:: P2RY10 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.78961494G>A, NC_000023.10:g.78216991G>A, NG_013276.2:g.21163G>A, NM_014499.4:c.974G>A, NM_014499.3:c.974G>A, NM_014499.2:c.974G>A, NM_198333.3:c.974G>A, NM_198333.2:c.974G>A, NM_198333.1:c.974G>A, NM_001324218.2:c.974G>A, NM_001324218.1:c.974G>A, NM_001324225.2:c.1049G>A, NM_001324225.1:c.1049G>A, NM_001324221.2:c.1025G>A, NM_001324221.1:c.1025G>A, XM_047441998.1:c.974G>A, NP_055314.1:p.Arg325His, NP_938147.1:p.Arg325His, NP_001311147.1:p.Arg325His, NP_001311154.1:p.Arg350His, NP_001311150.1:p.Arg342His, XP_047297954.1:p.Arg325His

Select item 14682034305.

rs1468203430 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:78961500 (GRCh38)
X:78216997 (GRCh37)
Canonical SPDI:: NC_000023.11:78961499:G:A
Gene:: P2RY10 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.78961500G>A, NC_000023.10:g.78216997G>A, NG_013276.2:g.21169G>A, NM_014499.4:c.980G>A, NM_014499.3:c.980G>A, NM_014499.2:c.980G>A, NM_198333.3:c.980G>A, NM_198333.2:c.980G>A, NM_198333.1:c.980G>A, NM_001324218.2:c.980G>A, NM_001324218.1:c.980G>A, NM_001324225.2:c.1055G>A, NM_001324225.1:c.1055G>A, NM_001324221.2:c.1031G>A, NM_001324221.1:c.1031G>A, XM_047441998.1:c.980G>A, NP_055314.1:p.Arg327His, NP_938147.1:p.Arg327His, NP_001311147.1:p.Arg327His, NP_001311154.1:p.Arg352His, NP_001311150.1:p.Arg344His, XP_047297954.1:p.Arg327His

Select item 14677384766.

rs1467738476 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:78961162 (GRCh38)
X:78216659 (GRCh37)
Canonical SPDI:: NC_000023.11:78961161:C:T
Gene:: P2RY10 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.78961162C>T, NC_000023.10:g.78216659C>T, NG_013276.2:g.20831C>T, NM_014499.4:c.642C>T, NM_014499.3:c.642C>T, NM_014499.2:c.642C>T, NM_198333.3:c.642C>T, NM_198333.2:c.642C>T, NM_198333.1:c.642C>T, NM_001324218.2:c.642C>T, NM_001324218.1:c.642C>T, NM_001324225.2:c.717C>T, NM_001324225.1:c.717C>T, NM_001324221.2:c.693C>T, NM_001324221.1:c.693C>T, XM_047441998.1:c.642C>T

Select item 14676945547.

rs1467694554 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: X:78961059 (GRCh38)
X:78216556 (GRCh37)
Canonical SPDI:: NC_000023.11:78961058:C:A
Gene:: P2RY10 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.78961059C>A, NC_000023.10:g.78216556C>A, NG_013276.2:g.20728C>A, NM_014499.4:c.539C>A, NM_014499.3:c.539C>A, NM_014499.2:c.539C>A, NM_198333.3:c.539C>A, NM_198333.2:c.539C>A, NM_198333.1:c.539C>A, NM_001324218.2:c.539C>A, NM_001324218.1:c.539C>A, NM_001324225.2:c.614C>A, NM_001324225.1:c.614C>A, NM_001324221.2:c.590C>A, NM_001324221.1:c.590C>A, XM_047441998.1:c.539C>A, NP_055314.1:p.Ser180Tyr, NP_938147.1:p.Ser180Tyr, NP_001311147.1:p.Ser180Tyr, NP_001311154.1:p.Ser205Tyr, NP_001311150.1:p.Ser197Tyr, XP_047297954.1:p.Ser180Tyr

Select item 14664104238.

rs1466410423 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:78961244 (GRCh38)
X:78216741 (GRCh37)
Canonical SPDI:: NC_000023.11:78961243:C:T
Gene:: P2RY10 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.78961244C>T, NC_000023.10:g.78216741C>T, NG_013276.2:g.20913C>T, NM_014499.4:c.724C>T, NM_014499.3:c.724C>T, NM_014499.2:c.724C>T, NM_198333.3:c.724C>T, NM_198333.2:c.724C>T, NM_198333.1:c.724C>T, NM_001324218.2:c.724C>T, NM_001324218.1:c.724C>T, NM_001324225.2:c.799C>T, NM_001324225.1:c.799C>T, NM_001324221.2:c.775C>T, NM_001324221.1:c.775C>T, XM_047441998.1:c.724C>T

Select item 14584457659.

rs1458445765 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:78960589 (GRCh38)
X:78216086 (GRCh37)
Canonical SPDI:: NC_000023.11:78960588:T:C
Gene:: P2RY10 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.78960589T>C, NC_000023.10:g.78216086T>C, NG_013276.2:g.20258T>C, NM_014499.4:c.69T>C, NM_014499.3:c.69T>C, NM_014499.2:c.69T>C, NM_198333.3:c.69T>C, NM_198333.2:c.69T>C, NM_198333.1:c.69T>C, NM_001324218.2:c.69T>C, NM_001324218.1:c.69T>C, NM_001324225.2:c.144T>C, NM_001324225.1:c.144T>C, NM_001324221.2:c.120T>C, NM_001324221.1:c.120T>C, XM_047441998.1:c.69T>C

Select item 145324297710.

rs1453242977 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:78961260 (GRCh38)
X:78216757 (GRCh37)
Canonical SPDI:: NC_000023.11:78961259:T:C
Gene:: P2RY10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000019/2 (GnomAD)
C=0.000023/6 (TOPMED)
HGVS:: NC_000023.11:g.78961260T>C, NC_000023.10:g.78216757T>C, NG_013276.2:g.20929T>C, NM_014499.4:c.740T>C, NM_014499.3:c.740T>C, NM_014499.2:c.740T>C, NM_198333.3:c.740T>C, NM_198333.2:c.740T>C, NM_198333.1:c.740T>C, NM_001324218.2:c.740T>C, NM_001324218.1:c.740T>C, NM_001324225.2:c.815T>C, NM_001324225.1:c.815T>C, NM_001324221.2:c.791T>C, NM_001324221.1:c.791T>C, XM_047441998.1:c.740T>C, NP_055314.1:p.Met247Thr, NP_938147.1:p.Met247Thr, NP_001311147.1:p.Met247Thr, NP_001311154.1:p.Met272Thr, NP_001311150.1:p.Met264Thr, XP_047297954.1:p.Met247Thr

Select item 145309419511.

rs1453094195 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: X:78961389 (GRCh38)
X:78216886 (GRCh37)
Canonical SPDI:: NC_000023.11:78961388:G:C
Gene:: P2RY10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.78961389G>C, NC_000023.10:g.78216886G>C, NG_013276.2:g.21058G>C, NM_014499.4:c.869G>C, NM_014499.3:c.869G>C, NM_014499.2:c.869G>C, NM_198333.3:c.869G>C, NM_198333.2:c.869G>C, NM_198333.1:c.869G>C, NM_001324218.2:c.869G>C, NM_001324218.1:c.869G>C, NM_001324225.2:c.944G>C, NM_001324225.1:c.944G>C, NM_001324221.2:c.920G>C, NM_001324221.1:c.920G>C, XM_047441998.1:c.869G>C, NP_055314.1:p.Cys290Ser, NP_938147.1:p.Cys290Ser, NP_001311147.1:p.Cys290Ser, NP_001311154.1:p.Cys315Ser, NP_001311150.1:p.Cys307Ser, XP_047297954.1:p.Cys290Ser

Select item 144759370412.

rs1447593704 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:78960676 (GRCh38)
X:78216173 (GRCh37)
Canonical SPDI:: NC_000023.11:78960675:C:T
Gene:: P2RY10 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.78960676C>T, NC_000023.10:g.78216173C>T, NG_013276.2:g.20345C>T, NM_014499.4:c.156C>T, NM_014499.3:c.156C>T, NM_014499.2:c.156C>T, NM_198333.3:c.156C>T, NM_198333.2:c.156C>T, NM_198333.1:c.156C>T, NM_001324218.2:c.156C>T, NM_001324218.1:c.156C>T, NM_001324225.2:c.231C>T, NM_001324225.1:c.231C>T, NM_001324221.2:c.207C>T, NM_001324221.1:c.207C>T, XM_047441998.1:c.156C>T

Select item 144444414713.

rs1444444147 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:78961515 (GRCh38)
X:78217012 (GRCh37)
Canonical SPDI:: NC_000023.11:78961514:A:G
Gene:: P2RY10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.78961515A>G, NC_000023.10:g.78217012A>G, NG_013276.2:g.21184A>G, NM_014499.4:c.995A>G, NM_014499.3:c.995A>G, NM_014499.2:c.995A>G, NM_198333.3:c.995A>G, NM_198333.2:c.995A>G, NM_198333.1:c.995A>G, NM_001324218.2:c.995A>G, NM_001324218.1:c.995A>G, NM_001324225.2:c.1070A>G, NM_001324225.1:c.1070A>G, NM_001324221.2:c.1046A>G, NM_001324221.1:c.1046A>G, XM_047441998.1:c.995A>G, NP_055314.1:p.Glu332Gly, NP_938147.1:p.Glu332Gly, NP_001311147.1:p.Glu332Gly, NP_001311154.1:p.Glu357Gly, NP_001311150.1:p.Glu349Gly, XP_047297954.1:p.Glu332Gly

Select item 144166334514.

rs1441663345 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: X:78961097 (GRCh38)
X:78216594 (GRCh37)
Canonical SPDI:: NC_000023.11:78961096:G:C
Gene:: P2RY10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000005/1 (GnomAD_exomes)
C=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.78961097G>C, NC_000023.10:g.78216594G>C, NG_013276.2:g.20766G>C, NM_014499.4:c.577G>C, NM_014499.3:c.577G>C, NM_014499.2:c.577G>C, NM_198333.3:c.577G>C, NM_198333.2:c.577G>C, NM_198333.1:c.577G>C, NM_001324218.2:c.577G>C, NM_001324218.1:c.577G>C, NM_001324225.2:c.652G>C, NM_001324225.1:c.652G>C, NM_001324221.2:c.628G>C, NM_001324221.1:c.628G>C, XM_047441998.1:c.577G>C, NP_055314.1:p.Val193Leu, NP_938147.1:p.Val193Leu, NP_001311147.1:p.Val193Leu, NP_001311154.1:p.Val218Leu, NP_001311150.1:p.Val210Leu, XP_047297954.1:p.Val193Leu

Select item 143408732415.

rs1434087324 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:78960925 (GRCh38)
X:78216422 (GRCh37)
Canonical SPDI:: NC_000023.11:78960924:C:T
Gene:: P2RY10 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.78960925C>T, NC_000023.10:g.78216422C>T, NG_013276.2:g.20594C>T, NM_014499.4:c.405C>T, NM_014499.3:c.405C>T, NM_014499.2:c.405C>T, NM_198333.3:c.405C>T, NM_198333.2:c.405C>T, NM_198333.1:c.405C>T, NM_001324218.2:c.405C>T, NM_001324218.1:c.405C>T, NM_001324225.2:c.480C>T, NM_001324225.1:c.480C>T, NM_001324221.2:c.456C>T, NM_001324221.1:c.456C>T, XM_047441998.1:c.405C>T

Select item 142728496116.

rs1427284961 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:78961478 (GRCh38)
X:78216975 (GRCh37)
Canonical SPDI:: NC_000023.11:78961477:G:A
Gene:: P2RY10 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: A=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.78961478G>A, NC_000023.10:g.78216975G>A, NG_013276.2:g.21147G>A, NM_014499.4:c.958G>A, NM_014499.3:c.958G>A, NM_014499.2:c.958G>A, NM_198333.3:c.958G>A, NM_198333.2:c.958G>A, NM_198333.1:c.958G>A, NM_001324218.2:c.958G>A, NM_001324218.1:c.958G>A, NM_001324225.2:c.1033G>A, NM_001324225.1:c.1033G>A, NM_001324221.2:c.1009G>A, NM_001324221.1:c.1009G>A, XM_047441998.1:c.958G>A, NP_055314.1:p.Gly320Ser, NP_938147.1:p.Gly320Ser, NP_001311147.1:p.Gly320Ser, NP_001311154.1:p.Gly345Ser, NP_001311150.1:p.Gly337Ser, XP_047297954.1:p.Gly320Ser

Select item 142243617017.

rs1422436170 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:78960897 (GRCh38)
X:78216394 (GRCh37)
Canonical SPDI:: NC_000023.11:78960896:G:A
Gene:: P2RY10 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000023.11:g.78960897G>A, NC_000023.10:g.78216394G>A, NG_013276.2:g.20566G>A, NM_014499.4:c.377G>A, NM_014499.3:c.377G>A, NM_014499.2:c.377G>A, NM_198333.3:c.377G>A, NM_198333.2:c.377G>A, NM_198333.1:c.377G>A, NM_001324218.2:c.377G>A, NM_001324218.1:c.377G>A, NM_001324225.2:c.452G>A, NM_001324225.1:c.452G>A, NM_001324221.2:c.428G>A, NM_001324221.1:c.428G>A, XM_047441998.1:c.377G>A, NP_055314.1:p.Cys126Tyr, NP_938147.1:p.Cys126Tyr, NP_001311147.1:p.Cys126Tyr, NP_001311154.1:p.Cys151Tyr, NP_001311150.1:p.Cys143Tyr, XP_047297954.1:p.Cys126Tyr

Select item 142201590118.

rs1422015901 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:78960689 (GRCh38)
X:78216186 (GRCh37)
Canonical SPDI:: NC_000023.11:78960688:T:C
Gene:: P2RY10 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.78960689T>C, NC_000023.10:g.78216186T>C, NG_013276.2:g.20358T>C, NM_014499.4:c.169T>C, NM_014499.3:c.169T>C, NM_014499.2:c.169T>C, NM_198333.3:c.169T>C, NM_198333.2:c.169T>C, NM_198333.1:c.169T>C, NM_001324218.2:c.169T>C, NM_001324218.1:c.169T>C, NM_001324225.2:c.244T>C, NM_001324225.1:c.244T>C, NM_001324221.2:c.220T>C, NM_001324221.1:c.220T>C, XM_047441998.1:c.169T>C, NP_055314.1:p.Trp57Arg, NP_938147.1:p.Trp57Arg, NP_001311147.1:p.Trp57Arg, NP_001311154.1:p.Trp82Arg, NP_001311150.1:p.Trp74Arg, XP_047297954.1:p.Trp57Arg

Select item 141869728019.

rs1418697280 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:78961517 (GRCh38)
X:78217014 (GRCh37)
Canonical SPDI:: NC_000023.11:78961516:A:G
Gene:: P2RY10 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.78961517A>G, NC_000023.10:g.78217014A>G, NG_013276.2:g.21186A>G, NM_014499.4:c.997A>G, NM_014499.3:c.997A>G, NM_014499.2:c.997A>G, NM_198333.3:c.997A>G, NM_198333.2:c.997A>G, NM_198333.1:c.997A>G, NM_001324218.2:c.997A>G, NM_001324218.1:c.997A>G, NM_001324225.2:c.1072A>G, NM_001324225.1:c.1072A>G, NM_001324221.2:c.1048A>G, NM_001324221.1:c.1048A>G, XM_047441998.1:c.997A>G, NP_055314.1:p.Ser333Gly, NP_938147.1:p.Ser333Gly, NP_001311147.1:p.Ser333Gly, NP_001311154.1:p.Ser358Gly, NP_001311150.1:p.Ser350Gly, XP_047297954.1:p.Ser333Gly

Select item 141405856220.

rs1414058562 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: X:78960791 (GRCh38)
X:78216288 (GRCh37)
Canonical SPDI:: NC_000023.11:78960790:A:G,NC_000023.11:78960790:A:T
Gene:: P2RY10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
T=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.78960791A>G, NC_000023.11:g.78960791A>T, NC_000023.10:g.78216288A>G, NC_000023.10:g.78216288A>T, NG_013276.2:g.20460A>G, NG_013276.2:g.20460A>T, NM_014499.4:c.271A>G, NM_014499.4:c.271A>T, NM_014499.3:c.271A>G, NM_014499.3:c.271A>T, NM_014499.2:c.271A>G, NM_014499.2:c.271A>T, NM_198333.3:c.271A>G, NM_198333.3:c.271A>T, NM_198333.2:c.271A>G, NM_198333.2:c.271A>T, NM_198333.1:c.271A>G, NM_198333.1:c.271A>T, NM_001324218.2:c.271A>G, NM_001324218.2:c.271A>T, NM_001324218.1:c.271A>G, NM_001324218.1:c.271A>T, NM_001324225.2:c.346A>G, NM_001324225.2:c.346A>T, NM_001324225.1:c.346A>G, NM_001324225.1:c.346A>T, NM_001324221.2:c.322A>G, NM_001324221.2:c.322A>T, NM_001324221.1:c.322A>G, NM_001324221.1:c.322A>T, XM_047441998.1:c.271A>G, XM_047441998.1:c.271A>T, NP_055314.1:p.Ile91Val, NP_055314.1:p.Ile91Phe, NP_938147.1:p.Ile91Val, NP_938147.1:p.Ile91Phe, NP_001311147.1:p.Ile91Val, NP_001311147.1:p.Ile91Phe, NP_001311154.1:p.Ile116Val, NP_001311154.1:p.Ile116Phe, NP_001311150.1:p.Ile108Val, NP_001311150.1:p.Ile108Phe, XP_047297954.1:p.Ile91Val, XP_047297954.1:p.Ile91Phe

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