SNP Links for Protein (Select 13518017) - SNP

Links from Protein

Items: 1 to 20 of 333

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Select item 14904946261.

rs1490494626 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:112517273 (GRCh38)
1:113059895 (GRCh37)
Canonical SPDI:: NC_000001.11:112517272:C:T
Gene:: WNT2B (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: T=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.112517273C>T, NC_000001.10:g.113059895C>T, NG_052953.1:g.55733C>T, NM_004185.4:c.777C>T, NM_004185.3:c.777C>T, NM_001291880.1:c.558C>T, NM_024494.3:c.834C>T, NM_024494.2:c.834C>T

Select item 14889134702.

rs1488913470 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 1:112517381 (GRCh38)
1:113060003 (GRCh37)
Canonical SPDI:: NC_000001.11:112517380:T:C,NC_000001.11:112517380:T:G
Gene:: WNT2B (Varview), ST7L (Varview)
Functional Consequence:: 500B_downstream_variant,synonymous_variant,downstream_transcript_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000015/4 (TOPMED)
HGVS:: NC_000001.11:g.112517381T>C, NC_000001.11:g.112517381T>G, NC_000001.10:g.113060003T>C, NC_000001.10:g.113060003T>G, NG_052953.1:g.55841T>C, NG_052953.1:g.55841T>G, NM_004185.4:c.885T>C, NM_004185.4:c.885T>G, NM_004185.3:c.885T>C, NM_004185.3:c.885T>G, NM_001291880.1:c.666T>C, NM_001291880.1:c.666T>G, NM_024494.3:c.942T>C, NM_024494.3:c.942T>G, NM_024494.2:c.942T>C, NM_024494.2:c.942T>G

Select item 14858594693.

rs1485859469 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 1:112517368 (GRCh38)
1:113059990 (GRCh37)
Canonical SPDI:: NC_000001.11:112517367:T:A
Gene:: WNT2B (Varview), ST7L (Varview)
Functional Consequence:: 500B_downstream_variant,missense_variant,downstream_transcript_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000001.11:g.112517368T>A, NC_000001.10:g.113059990T>A, NG_052953.1:g.55828T>A, NM_004185.4:c.872T>A, NM_004185.3:c.872T>A, NM_001291880.1:c.653T>A, NM_024494.3:c.929T>A, NM_024494.2:c.929T>A, NP_004176.2:p.Val291Asp, NP_001278809.1:p.Val218Asp, NP_078613.1:p.Val310Asp

Select item 14838177544.

rs1483817754 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 1:112491037 (GRCh38)
1:113033659 (GRCh37)
Canonical SPDI:: NC_000001.11:112491036:A:C,NC_000001.11:112491036:A:G
Gene:: WNT2B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.112491037A>C, NC_000001.11:g.112491037A>G, NC_000001.10:g.113033659A>C, NC_000001.10:g.113033659A>G, NG_052953.1:g.29497A>C, NG_052953.1:g.29497A>G, NM_004185.4:c.81A>C, NM_004185.4:c.81A>G, NM_004185.3:c.81A>C, NM_004185.3:c.81A>G

Select item 14745674975.

rs1474567497 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:112467548 (GRCh38)
1:113010170 (GRCh37)
Canonical SPDI:: NC_000001.11:112467547:G:A
Gene:: WNT2B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,missense_variant,5_prime_UTR_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 (TOPMED)
HGVS:: NC_000001.11:g.112467548G>A, NC_000001.10:g.113010170G>A, NG_052953.1:g.6008G>A, NM_004185.4:c.11G>A, NM_004185.3:c.11G>A, NM_001291880.1:c.-138G>A, NP_004176.2:p.Gly4Asp

Select item 14735272576.

rs1473527257 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:112467571 (GRCh38)
1:113010193 (GRCh37)
Canonical SPDI:: NC_000001.11:112467570:A:G
Gene:: WNT2B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,missense_variant,5_prime_UTR_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.112467571A>G, NC_000001.10:g.113010193A>G, NG_052953.1:g.6031A>G, NM_004185.4:c.34A>G, NM_004185.3:c.34A>G, NM_001291880.1:c.-115A>G, NP_004176.2:p.Ile12Val

Select item 14695663077.

rs1469566307 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:112516224 (GRCh38)
1:113058846 (GRCh37)
Canonical SPDI:: NC_000001.11:112516223:T:C
Gene:: WNT2B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.112516224T>C, NC_000001.10:g.113058846T>C, NG_052953.1:g.54684T>C, NM_004185.4:c.431T>C, NM_004185.3:c.431T>C, NM_001291880.1:c.212T>C, NM_024494.3:c.488T>C, NM_024494.2:c.488T>C, NP_004176.2:p.Leu144Pro, NP_001278809.1:p.Leu71Pro, NP_078613.1:p.Leu163Pro

Select item 14691426988.

rs1469142698 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:112520384 (GRCh38)
1:113063006 (GRCh37)
Canonical SPDI:: NC_000001.11:112520383:C:T
Gene:: WNT2B (Varview), ST7L (Varview)
Functional Consequence:: missense_variant,genic_downstream_transcript_variant,coding_sequence_variant,intron_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.112520384C>T, NC_000001.10:g.113063006C>T, NG_052953.1:g.58844C>T, NM_004185.4:c.994C>T, NM_004185.3:c.994C>T, NM_001291880.1:c.775C>T, NM_024494.3:c.1051C>T, NM_024494.2:c.1051C>T, NP_004176.2:p.Arg332Cys, NP_001278809.1:p.Arg259Cys, NP_078613.1:p.Arg351Cys

Select item 14638544119.

rs1463854411 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 1:112516406 (GRCh38)
1:113059028 (GRCh37)
Canonical SPDI:: NC_000001.11:112516405:T:G
Gene:: WNT2B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.112516406T>G, NC_000001.10:g.113059028T>G, NG_052953.1:g.54866T>G, NM_004185.4:c.613T>G, NM_004185.3:c.613T>G, NM_001291880.1:c.394T>G, NM_024494.3:c.670T>G, NM_024494.2:c.670T>G, NP_004176.2:p.Cys205Gly, NP_001278809.1:p.Cys132Gly, NP_078613.1:p.Cys224Gly

Select item 146375528810.

rs1463755288 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 1:112520490 (GRCh38)
1:113063112 (GRCh37)
Canonical SPDI:: NC_000001.11:112520489:A:T
Gene:: WNT2B (Varview), ST7L (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant,genic_downstream_transcript_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.112520490A>T, NC_000001.10:g.113063112A>T, NG_052953.1:g.58950A>T, NM_004185.4:c.1100A>T, NM_004185.3:c.1100A>T, NM_001291880.1:c.881A>T, NM_024494.3:c.1157A>T, NM_024494.2:c.1157A>T, NP_004176.2:p.Glu367Val, NP_001278809.1:p.Glu294Val, NP_078613.1:p.Glu386Val

Select item 144783750511.

rs1447837505 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:112517184 (GRCh38)
1:113059806 (GRCh37)
Canonical SPDI:: NC_000001.11:112517183:C:T
Gene:: WNT2B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.112517184C>T, NC_000001.10:g.113059806C>T, NG_052953.1:g.55644C>T, NM_004185.4:c.688C>T, NM_004185.3:c.688C>T, NM_001291880.1:c.469C>T, NM_024494.3:c.745C>T, NM_024494.2:c.745C>T, NP_004176.2:p.Arg230Cys, NP_001278809.1:p.Arg157Cys, NP_078613.1:p.Arg249Cys

Select item 144655968612.

rs1446559686 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:112515032 (GRCh38)
1:113057654 (GRCh37)
Canonical SPDI:: NC_000001.11:112515031:A:G
Gene:: WNT2B (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.112515032A>G, NC_000001.10:g.113057654A>G, NG_052953.1:g.53492A>G, NM_004185.4:c.284A>G, NM_004185.3:c.284A>G, NM_001291880.1:c.65A>G, NM_024494.3:c.341A>G, NM_024494.2:c.341A>G, NP_004176.2:p.His95Arg, NP_001278809.1:p.His22Arg, NP_078613.1:p.His114Arg

Select item 144605006613.

rs1446050066 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 1:112517283 (GRCh38)
1:113059905 (GRCh37)
Canonical SPDI:: NC_000001.11:112517282:G:C
Gene:: WNT2B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.112517283G>C, NC_000001.10:g.113059905G>C, NG_052953.1:g.55743G>C, NM_004185.4:c.787G>C, NM_004185.3:c.787G>C, NM_001291880.1:c.568G>C, NM_024494.3:c.844G>C, NM_024494.2:c.844G>C, NP_004176.2:p.Ala263Pro, NP_001278809.1:p.Ala190Pro, NP_078613.1:p.Ala282Pro

Select item 144435289514.

rs1444352895 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 1:112516350 (GRCh38)
1:113058972 (GRCh37)
Canonical SPDI:: NC_000001.11:112516349:C:G,NC_000001.11:112516349:C:T
Gene:: WNT2B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: T=0.000004/1 (GnomAD_exomes)
G=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.112516350C>G, NC_000001.11:g.112516350C>T, NC_000001.10:g.113058972C>G, NC_000001.10:g.113058972C>T, NG_052953.1:g.54810C>G, NG_052953.1:g.54810C>T, NM_004185.4:c.557C>G, NM_004185.4:c.557C>T, NM_004185.3:c.557C>G, NM_004185.3:c.557C>T, NM_001291880.1:c.338C>G, NM_001291880.1:c.338C>T, NM_024494.3:c.614C>G, NM_024494.3:c.614C>T, NM_024494.2:c.614C>G, NM_024494.2:c.614C>T, NP_004176.2:p.Ala186Gly, NP_004176.2:p.Ala186Val, NP_001278809.1:p.Ala113Gly, NP_001278809.1:p.Ala113Val, NP_078613.1:p.Ala205Gly, NP_078613.1:p.Ala205Val

Select item 144384876515.

rs1443848765 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:112520406 (GRCh38)
1:113063028 (GRCh37)
Canonical SPDI:: NC_000001.11:112520405:A:G
Gene:: WNT2B (Varview), ST7L (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,genic_downstream_transcript_variant,intron_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.112520406A>G, NC_000001.10:g.113063028A>G, NG_052953.1:g.58866A>G, NM_004185.4:c.1016A>G, NM_004185.3:c.1016A>G, NM_001291880.1:c.797A>G, NM_024494.3:c.1073A>G, NM_024494.2:c.1073A>G, NP_004176.2:p.Lys339Arg, NP_001278809.1:p.Lys266Arg, NP_078613.1:p.Lys358Arg

Select item 144086884416.

rs1440868844 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:112520358 (GRCh38)
1:113062980 (GRCh37)
Canonical SPDI:: NC_000001.11:112520357:G:A
Gene:: WNT2B (Varview), ST7L (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.112520358G>A, NC_000001.10:g.113062980G>A, NG_052953.1:g.58818G>A, NM_004185.4:c.968G>A, NM_004185.3:c.968G>A, NM_001291880.1:c.749G>A, NM_024494.3:c.1025G>A, NM_024494.2:c.1025G>A, NP_004176.2:p.Arg323Gln, NP_001278809.1:p.Arg250Gln, NP_078613.1:p.Arg342Gln

Select item 143993167217.

rs1439931672 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:112517129 (GRCh38)
1:113059751 (GRCh37)
Canonical SPDI:: NC_000001.11:112517128:G:T
Gene:: WNT2B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.112517129G>T, NC_000001.10:g.113059751G>T, NG_052953.1:g.55589G>T, NM_004185.4:c.633G>T, NM_004185.3:c.633G>T, NM_001291880.1:c.414G>T, NM_024494.3:c.690G>T, NM_024494.2:c.690G>T

Select item 143869901218.

rs1438699012 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:112514926 (GRCh38)
1:113057548 (GRCh37)
Canonical SPDI:: NC_000001.11:112514925:G:A
Gene:: WNT2B (Varview)
Functional Consequence:: coding_sequence_variant,5_prime_UTR_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.112514926G>A, NC_000001.10:g.113057548G>A, NG_052953.1:g.53386G>A, NM_004185.4:c.178G>A, NM_004185.3:c.178G>A, NM_001291880.1:c.-42G>A, NM_024494.3:c.235G>A, NM_024494.2:c.235G>A, NP_004176.2:p.Val60Met, NP_078613.1:p.Val79Met

Select item 143842778719.

rs1438427787 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:112520424 (GRCh38)
1:113063046 (GRCh37)
Canonical SPDI:: NC_000001.11:112520423:C:T
Gene:: WNT2B (Varview), ST7L (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.112520424C>T, NC_000001.10:g.113063046C>T, NG_052953.1:g.58884C>T, NM_004185.4:c.1034C>T, NM_004185.3:c.1034C>T, NM_001291880.1:c.815C>T, NM_024494.3:c.1091C>T, NM_024494.2:c.1091C>T, NP_004176.2:p.Ala345Val, NP_001278809.1:p.Ala272Val, NP_078613.1:p.Ala364Val

Select item 143839279820.

rs1438392798 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 1:112514971 (GRCh38)
1:113057593 (GRCh37)
Canonical SPDI:: NC_000001.11:112514970:C:A,NC_000001.11:112514970:C:T
Gene:: WNT2B (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)
HGVS:: NC_000001.11:g.112514971C>A, NC_000001.11:g.112514971C>T, NC_000001.10:g.113057593C>A, NC_000001.10:g.113057593C>T, NG_052953.1:g.53431C>A, NG_052953.1:g.53431C>T, NM_004185.4:c.223C>A, NM_004185.4:c.223C>T, NM_004185.3:c.223C>A, NM_004185.3:c.223C>T, NM_001291880.1:c.4C>A, NM_001291880.1:c.4C>T, NM_024494.3:c.280C>A, NM_024494.3:c.280C>T, NM_024494.2:c.280C>A, NM_024494.2:c.280C>T, NP_004176.2:p.Arg75Ser, NP_004176.2:p.Arg75Cys, NP_001278809.1:p.Arg2Ser, NP_001278809.1:p.Arg2Cys, NP_078613.1:p.Arg94Ser, NP_078613.1:p.Arg94Cys

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