SNP Links for Protein (Select 1238280272) - SNP

Links from Protein

Items: 1 to 20 of 407

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Select item 14903909281.

rs1490390928 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:35059147 (GRCh38)
9:35059144 (GRCh37)
Canonical SPDI:: NC_000009.12:35059146:G:A
Gene:: VCP (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Clinical significance:: likely-pathogenic
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.35059147G>A, NC_000009.11:g.35059144G>A, NG_007887.1:g.18596C>T, NM_007126.5:c.2077C>T, NM_007126.4:c.2077C>T, NM_007126.3:c.2077C>T, NM_001354928.2:c.1942C>T, NM_001354928.1:c.1942C>T, NM_001354927.2:c.1942C>T, NM_001354927.1:c.1942C>T, NP_009057.1:p.Arg693Cys, NP_001341857.1:p.Arg648Cys, NP_001341856.1:p.Arg648Cys

Select item 14879791552.

rs1487979155 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:35067993 (GRCh38)
9:35067990 (GRCh37)
Canonical SPDI:: NC_000009.12:35067992:G:A
Gene:: VCP (Varview)
Functional Consequence:: coding_sequence_variant,missense_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_000009.12:g.35067993G>A, NC_000009.11:g.35067990G>A, NG_007887.1:g.9750C>T, NM_007126.5:c.200C>T, NM_007126.4:c.200C>T, NM_007126.3:c.200C>T, NM_001354928.2:c.65C>T, NM_001354928.1:c.65C>T, NM_001354927.2:c.65C>T, NM_001354927.1:c.65C>T, NP_009057.1:p.Ala67Val, NP_001341857.1:p.Ala22Val, NP_001341856.1:p.Ala22Val

Select item 14845412203.

rs1484541220 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:35066808 (GRCh38)
9:35066805 (GRCh37)
Canonical SPDI:: NC_000009.12:35066807:T:C
Gene:: VCP (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Clinical significance:: likely-benign
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000009.12:g.35066808T>C, NC_000009.11:g.35066805T>C, NG_007887.1:g.10935A>G, NM_007126.5:c.312A>G, NM_007126.4:c.312A>G, NM_007126.3:c.312A>G, NM_001354928.2:c.177A>G, NM_001354928.1:c.177A>G, NM_001354927.2:c.177A>G, NM_001354927.1:c.177A>G

Select item 14819928454.

rs1481992845 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:35067986 (GRCh38)
9:35067983 (GRCh37)
Canonical SPDI:: NC_000009.12:35067985:G:A
Gene:: VCP (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.35067986G>A, NC_000009.11:g.35067983G>A, NG_007887.1:g.9757C>T, NM_007126.5:c.207C>T, NM_007126.4:c.207C>T, NM_007126.3:c.207C>T, NM_001354928.2:c.72C>T, NM_001354928.1:c.72C>T, NM_001354927.2:c.72C>T, NM_001354927.1:c.72C>T

Select item 14812903665.

rs1481290366 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:35060430 (GRCh38)
9:35060427 (GRCh37)
Canonical SPDI:: NC_000009.12:35060429:C:T
Gene:: VCP (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000009.12:g.35060430C>T, NC_000009.11:g.35060427C>T, NG_007887.1:g.17313G>A, NM_007126.5:c.1578G>A, NM_007126.4:c.1578G>A, NM_007126.3:c.1578G>A, NM_001354928.2:c.1443G>A, NM_001354928.1:c.1443G>A, NM_001354927.2:c.1443G>A, NM_001354927.1:c.1443G>A

Select item 14753559256.

rs1475355925 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:35060816 (GRCh38)
9:35060813 (GRCh37)
Canonical SPDI:: NC_000009.12:35060815:T:C
Gene:: VCP (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000009.12:g.35060816T>C, NC_000009.11:g.35060813T>C, NG_007887.1:g.16927A>G, NM_007126.5:c.1467A>G, NM_007126.4:c.1467A>G, NM_007126.3:c.1467A>G, NM_001354928.2:c.1332A>G, NM_001354928.1:c.1332A>G, NM_001354927.2:c.1332A>G, NM_001354927.1:c.1332A>G

Select item 14719293947.

rs1471929394 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:35061651 (GRCh38)
9:35061648 (GRCh37)
Canonical SPDI:: NC_000009.12:35061650:C:T
Gene:: VCP (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000224/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000223/1 (Estonian)
HGVS:: NC_000009.12:g.35061651C>T, NC_000009.11:g.35061648C>T, NG_007887.1:g.16092G>A, NM_007126.5:c.1120G>A, NM_007126.4:c.1120G>A, NM_007126.3:c.1120G>A, NM_001354928.2:c.985G>A, NM_001354928.1:c.985G>A, NM_001354927.2:c.985G>A, NM_001354927.1:c.985G>A, NP_009057.1:p.Ala374Thr, NP_001341857.1:p.Ala329Thr, NP_001341856.1:p.Ala329Thr

Select item 14713841698.

rs1471384169 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:35064244 (GRCh38)
9:35064241 (GRCh37)
Canonical SPDI:: NC_000009.12:35064243:A:G
Gene:: VCP (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Clinical significance:: likely-benign
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000028/1 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000019/5 (TOPMED)
HGVS:: NC_000009.12:g.35064244A>G, NC_000009.11:g.35064241A>G, NG_007887.1:g.13499T>C, NM_007126.5:c.618T>C, NM_007126.4:c.618T>C, NM_007126.3:c.618T>C, NM_001354928.2:c.483T>C, NM_001354928.1:c.483T>C, NM_001354927.2:c.483T>C, NM_001354927.1:c.483T>C

Select item 14707922089.

rs1470792208 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 9:35061593 (GRCh38)
9:35061590 (GRCh37)
Canonical SPDI:: NC_000009.12:35061592:T:C,NC_000009.12:35061592:T:G
Gene:: VCP (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: G=0.000004/1 (GnomAD_exomes)
C=0.000106/3 (TOMMO)
HGVS:: NC_000009.12:g.35061593T>C, NC_000009.12:g.35061593T>G, NC_000009.11:g.35061590T>C, NC_000009.11:g.35061590T>G, NG_007887.1:g.16150A>G, NG_007887.1:g.16150A>C, NM_007126.5:c.1178A>G, NM_007126.5:c.1178A>C, NM_007126.4:c.1178A>G, NM_007126.4:c.1178A>C, NM_007126.3:c.1178A>G, NM_007126.3:c.1178A>C, NM_001354928.2:c.1043A>G, NM_001354928.2:c.1043A>C, NM_001354928.1:c.1043A>G, NM_001354928.1:c.1043A>C, NM_001354927.2:c.1043A>G, NM_001354927.2:c.1043A>C, NM_001354927.1:c.1043A>G, NM_001354927.1:c.1043A>C, NP_009057.1:p.Asp393Gly, NP_009057.1:p.Asp393Ala, NP_001341857.1:p.Asp348Gly, NP_001341857.1:p.Asp348Ala, NP_001341856.1:p.Asp348Gly, NP_001341856.1:p.Asp348Ala

Select item 146145435310.

rs1461454353 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 9:35064220 (GRCh38)
9:35064217 (GRCh37)
Canonical SPDI:: NC_000009.12:35064219:A:C
Gene:: VCP (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.35064220A>C, NC_000009.11:g.35064217A>C, NG_007887.1:g.13523T>G, NM_007126.5:c.642T>G, NM_007126.4:c.642T>G, NM_007126.3:c.642T>G, NM_001354928.2:c.507T>G, NM_001354928.1:c.507T>G, NM_001354927.2:c.507T>G, NM_001354927.1:c.507T>G

Select item 145848132811.

rs1458481328 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:35060479 (GRCh38)
9:35060476 (GRCh37)
Canonical SPDI:: NC_000009.12:35060478:G:A
Gene:: VCP (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
HGVS:: NC_000009.12:g.35060479G>A, NC_000009.11:g.35060476G>A, NG_007887.1:g.17264C>T, NM_007126.5:c.1529C>T, NM_007126.4:c.1529C>T, NM_007126.3:c.1529C>T, NM_001354928.2:c.1394C>T, NM_001354928.1:c.1394C>T, NM_001354927.2:c.1394C>T, NM_001354927.1:c.1394C>T, NP_009057.1:p.Pro510Leu, NP_001341857.1:p.Pro465Leu, NP_001341856.1:p.Pro465Leu

Select item 145808820212.

rs1458088202 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:35068044 (GRCh38)
9:35068041 (GRCh37)
Canonical SPDI:: NC_000009.12:35068043:T:C
Gene:: VCP (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000011/3 (TOPMED)
C=0.000036/5 (GnomAD)
HGVS:: NC_000009.12:g.35068044T>C, NC_000009.11:g.35068041T>C, NG_007887.1:g.9699A>G, NM_007126.5:c.149A>G, NM_007126.4:c.149A>G, NM_007126.3:c.149A>G, NM_001354928.2:c.14A>G, NM_001354928.1:c.14A>G, NM_001354927.2:c.14A>G, NM_001354927.1:c.14A>G, NP_009057.1:p.Gln50Arg, NP_001341857.1:p.Gln5Arg, NP_001341856.1:p.Gln5Arg

Select item 145709332713.

rs1457093327 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:35061633 (GRCh38)
9:35061630 (GRCh37)
Canonical SPDI:: NC_000009.12:35061632:T:C
Gene:: VCP (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.35061633T>C, NC_000009.11:g.35061630T>C, NG_007887.1:g.16110A>G, NM_007126.5:c.1138A>G, NM_007126.4:c.1138A>G, NM_007126.3:c.1138A>G, NM_001354928.2:c.1003A>G, NM_001354928.1:c.1003A>G, NM_001354927.2:c.1003A>G, NM_001354927.1:c.1003A>G, NP_009057.1:p.Ile380Val, NP_001341857.1:p.Ile335Val, NP_001341856.1:p.Ile335Val

Select item 145701149714.

rs1457011497 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 9:35059640 (GRCh38)
9:35059637 (GRCh37)
Canonical SPDI:: NC_000009.12:35059639:G:A,NC_000009.12:35059639:G:C
Gene:: VCP (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.35059640G>A, NC_000009.12:g.35059640G>C, NC_000009.11:g.35059637G>A, NC_000009.11:g.35059637G>C, NG_007887.1:g.18103C>T, NG_007887.1:g.18103C>G, NM_007126.5:c.1857C>T, NM_007126.5:c.1857C>G, NM_007126.4:c.1857C>T, NM_007126.4:c.1857C>G, NM_007126.3:c.1857C>T, NM_007126.3:c.1857C>G, NM_001354928.2:c.1722C>T, NM_001354928.2:c.1722C>G, NM_001354928.1:c.1722C>T, NM_001354928.1:c.1722C>G, NM_001354927.2:c.1722C>T, NM_001354927.2:c.1722C>G, NM_001354927.1:c.1722C>T, NM_001354927.1:c.1722C>G, NP_009057.1:p.Ile619Met, NP_001341857.1:p.Ile574Met, NP_001341856.1:p.Ile574Met

Select item 144947074015.

rs1449470740 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 9:35062061 (GRCh38)
9:35062058 (GRCh37)
Canonical SPDI:: NC_000009.12:35062060:C:A
Gene:: VCP (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.35062061C>A, NC_000009.11:g.35062058C>A, NG_007887.1:g.15682G>T, NM_007126.5:c.1023G>T, NM_007126.4:c.1023G>T, NM_007126.3:c.1023G>T, NM_001354928.2:c.888G>T, NM_001354928.1:c.888G>T, NM_001354927.2:c.888G>T, NM_001354927.1:c.888G>T

Select item 144279035616.

rs1442790356 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:35057156 (GRCh38)
9:35057153 (GRCh37)
Canonical SPDI:: NC_000009.12:35057155:A:G
Gene:: VCP (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.35057156A>G, NC_000009.11:g.35057153A>G, NG_007887.1:g.20587T>C, NM_007126.5:c.2382T>C, NM_007126.4:c.2382T>C, NM_007126.3:c.2382T>C, NM_001354928.2:c.2247T>C, NM_001354928.1:c.2247T>C, NM_001354927.2:c.2247T>C, NM_001354927.1:c.2247T>C

Select item 144002418217.

rs1440024182 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:35059075 (GRCh38)
9:35059072 (GRCh37)
Canonical SPDI:: NC_000009.12:35059074:G:A
Gene:: VCP (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=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000009.12:g.35059075G>A, NC_000009.11:g.35059072G>A, NG_007887.1:g.18668C>T, NM_007126.5:c.2149C>T, NM_007126.4:c.2149C>T, NM_007126.3:c.2149C>T, NM_001354928.2:c.2014C>T, NM_001354928.1:c.2014C>T, NM_001354927.2:c.2014C>T, NM_001354927.1:c.2014C>T, NP_009057.1:p.Pro717Ser, NP_001341857.1:p.Pro672Ser, NP_001341856.1:p.Pro672Ser

Select item 143842345618.

rs1438423456 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:35059730 (GRCh38)
9:35059727 (GRCh37)
Canonical SPDI:: NC_000009.12:35059729:G:A
Gene:: VCP (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_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_000009.12:g.35059730G>A, NC_000009.11:g.35059727G>A, NG_007887.1:g.18013C>T, NM_007126.5:c.1767C>T, NM_007126.4:c.1767C>T, NM_007126.3:c.1767C>T, NM_001354928.2:c.1632C>T, NM_001354928.1:c.1632C>T, NM_001354927.2:c.1632C>T, NM_001354927.1:c.1632C>T

Select item 143763101619.

rs1437631016 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 9:35065317 (GRCh38)
9:35065314 (GRCh37)
Canonical SPDI:: NC_000009.12:35065316:A:C,NC_000009.12:35065316:A:G
Gene:: VCP (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000051/1 (ALFA)
G=0.000004/1 (TOPMED)
C=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000009.12:g.35065317A>C, NC_000009.12:g.35065317A>G, NC_000009.11:g.35065314A>C, NC_000009.11:g.35065314A>G, NG_007887.1:g.12426T>G, NG_007887.1:g.12426T>C, NM_007126.5:c.510T>G, NM_007126.5:c.510T>C, NM_007126.4:c.510T>G, NM_007126.4:c.510T>C, NM_007126.3:c.510T>G, NM_007126.3:c.510T>C, NM_001354928.2:c.375T>G, NM_001354928.2:c.375T>C, NM_001354928.1:c.375T>G, NM_001354928.1:c.375T>C, NM_001354927.2:c.375T>G, NM_001354927.2:c.375T>C, NM_001354927.1:c.375T>G, NM_001354927.1:c.375T>C

Select item 143528410220.

rs1435284102 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:35062280 (GRCh38)
9:35062277 (GRCh37)
Canonical SPDI:: NC_000009.12:35062279:C:T
Gene:: VCP (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by cluster
MAF:: T=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.35062280C>T, NC_000009.11:g.35062277C>T, NG_007887.1:g.15463G>A, NM_007126.5:c.882G>A, NM_007126.4:c.882G>A, NM_007126.3:c.882G>A, NM_001354928.2:c.747G>A, NM_001354928.1:c.747G>A, NM_001354927.2:c.747G>A, NM_001354927.1:c.747G>A

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