SNP Links for Protein (Select 14916475) - SNP

Links from Protein

Items: 1 to 20 of 330

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Select item 14892350251.

rs1489235025 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:228059145 (GRCh38)
1:228246846 (GRCh37)
Canonical SPDI:: NC_000001.11:228059144:C:T
Gene:: WNT3A (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)
HGVS:: NC_000001.11:g.228059145C>T, NC_000001.10:g.228246846C>T, NM_033131.4:c.739C>T, NM_033131.3:c.739C>T, NP_149122.1:p.Arg247Trp

Select item 14889676172.

rs1488967617 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:228022892 (GRCh38)
1:228210593 (GRCh37)
Canonical SPDI:: NC_000001.11:228022891:G:T
Gene:: WNT3A (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.228022892G>T, NC_000001.10:g.228210593G>T, NM_033131.4:c.297G>T, NM_033131.3:c.297G>T

Select item 14889103563.

rs1488910356 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:228059447 (GRCh38)
1:228247148 (GRCh37)
Canonical SPDI:: NC_000001.11:228059446:C:A
Gene:: WNT3A (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000001.11:g.228059447C>A, NC_000001.10:g.228247148C>A, NM_033131.4:c.1041C>A, NM_033131.3:c.1041C>A, NP_149122.1:p.Asp347Glu

Select item 14885745294.

rs1488574529 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:228050814 (GRCh38)
1:228238515 (GRCh37)
Canonical SPDI:: NC_000001.11:228050813:G:A
Gene:: WNT3A (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Clinical significance:: uncertain-significance
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000019/5 (TOPMED)
HGVS:: NC_000001.11:g.228050814G>A, NC_000001.10:g.228238515G>A, NM_033131.4:c.472G>A, NM_033131.3:c.472G>A, NP_149122.1:p.Asp158Asn

Select item 14879885435.

rs1487988543 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:228007167 (GRCh38)
1:228194868 (GRCh37)
Canonical SPDI:: NC_000001.11:228007166:G:A
Gene:: WNT3A (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.228007167G>A, NC_000001.10:g.228194868G>A, NM_033131.4:c.39G>A, NM_033131.3:c.39G>A

Select item 14876986986.

rs1487698698 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:228050921 (GRCh38)
1:228238622 (GRCh37)
Canonical SPDI:: NC_000001.11:228050920:G:A
Gene:: WNT3A (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000005/1 (GnomAD_exomes)
A=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.228050921G>A, NC_000001.10:g.228238622G>A, NM_033131.4:c.579G>A, NM_033131.3:c.579G>A

Select item 14858285087.

rs1485828508 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:228050853 (GRCh38)
1:228238554 (GRCh37)
Canonical SPDI:: NC_000001.11:228050852:G:A
Gene:: WNT3A (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)
A=0.000035/1 (TOMMO)
HGVS:: NC_000001.11:g.228050853G>A, NC_000001.10:g.228238554G>A, NM_033131.4:c.511G>A, NM_033131.3:c.511G>A, NP_149122.1:p.Asp171Asn

Select item 14843782848.

rs1484378284 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:228050766 (GRCh38)
1:228238467 (GRCh37)
Canonical SPDI:: NC_000001.11:228050765:C:A
Gene:: WNT3A (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.228050766C>A, NC_000001.10:g.228238467C>A, NM_033131.4:c.424C>A, NM_033131.3:c.424C>A, NP_149122.1:p.His142Asn

Select item 14797852409.

rs1479785240 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:228059375 (GRCh38)
1:228247076 (GRCh37)
Canonical SPDI:: NC_000001.11:228059374:C:T
Gene:: WNT3A (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.228059375C>T, NC_000001.10:g.228247076C>T, NM_033131.4:c.969C>T, NM_033131.3:c.969C>T

Select item 147865489010.

rs1478654890 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:228059058 (GRCh38)
1:228246759 (GRCh37)
Canonical SPDI:: NC_000001.11:228059057:T:C
Gene:: WNT3A (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.228059058T>C, NC_000001.10:g.228246759T>C, NM_033131.4:c.652T>C, NM_033131.3:c.652T>C, NP_149122.1:p.Trp218Arg

Select item 147827331411.

rs1478273314 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:228059161 (GRCh38)
1:228246862 (GRCh37)
Canonical SPDI:: NC_000001.11:228059160:G:T
Gene:: WNT3A (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.228059161G>T, NC_000001.10:g.228246862G>T, NM_033131.4:c.755G>T, NM_033131.3:c.755G>T, NP_149122.1:p.Trp252Leu

Select item 147822775012.

rs1478227750 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:228050776 (GRCh38)
1:228238477 (GRCh37)
Canonical SPDI:: NC_000001.11:228050775:C:T
Gene:: WNT3A (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.228050776C>T, NC_000001.10:g.228238477C>T, NM_033131.4:c.434C>T, NM_033131.3:c.434C>T, NP_149122.1:p.Ser145Leu

Select item 147626655513.

rs1476266555 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 1:228059381 (GRCh38)
1:228247082 (GRCh37)
Canonical SPDI:: NC_000001.11:228059380:G:A,NC_000001.11:228059380:G:T
Gene:: WNT3A (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
A=0.000006/1 (GnomAD_exomes)
T=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.228059381G>A, NC_000001.11:g.228059381G>T, NC_000001.10:g.228247082G>A, NC_000001.10:g.228247082G>T, NM_033131.4:c.975G>A, NM_033131.4:c.975G>T, NM_033131.3:c.975G>A, NM_033131.3:c.975G>T, NP_149122.1:p.Glu325Asp

Select item 146791656814.

rs1467916568 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:228059293 (GRCh38)
1:228246994 (GRCh37)
Canonical SPDI:: NC_000001.11:228059292:C:T
Gene:: WNT3A (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.228059293C>T, NC_000001.10:g.228246994C>T, NM_033131.4:c.887C>T, NM_033131.3:c.887C>T, NP_149122.1:p.Thr296Ile

Select item 146726944815.

rs1467269448 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 1:228050810 (GRCh38)
1:228238511 (GRCh37)
Canonical SPDI:: NC_000001.11:228050809:C:A,NC_000001.11:228050809:C:T
Gene:: WNT3A (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.228050810C>A, NC_000001.11:g.228050810C>T, NC_000001.10:g.228238511C>A, NC_000001.10:g.228238511C>T, NM_033131.4:c.468C>A, NM_033131.4:c.468C>T, NM_033131.3:c.468C>A, NM_033131.3:c.468C>T, NP_149122.1:p.Ser156Arg

Select item 146653894216.

rs1466538942 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 1:228022771 (GRCh38)
1:228210472 (GRCh37)
Canonical SPDI:: NC_000001.11:228022770:A:T
Gene:: WNT3A (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.228022771A>T, NC_000001.10:g.228210472A>T, NM_033131.4:c.176A>T, NM_033131.3:c.176A>T, NP_149122.1:p.Tyr59Phe

Select item 146650752217.

rs1466507522 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:228059318 (GRCh38)
1:228247019 (GRCh37)
Canonical SPDI:: NC_000001.11:228059317:C:T
Gene:: WNT3A (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Clinical significance:: likely-benign
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.228059318C>T, NC_000001.10:g.228247019C>T, NM_033131.4:c.912C>T, NM_033131.3:c.912C>T

Select item 146546831818.

rs1465468318 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 1:228050723 (GRCh38)
1:228238424 (GRCh37)
Canonical SPDI:: NC_000001.11:228050722:A:C,NC_000001.11:228050722:A:G
Gene:: WNT3A (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
C=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.228050723A>C, NC_000001.11:g.228050723A>G, NC_000001.10:g.228238424A>C, NC_000001.10:g.228238424A>G, NM_033131.4:c.381A>C, NM_033131.4:c.381A>G, NM_033131.3:c.381A>C, NM_033131.3:c.381A>G

Select item 145964099619.

rs1459640996 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 1:228059322 (GRCh38)
1:228247023 (GRCh37)
Canonical SPDI:: NC_000001.11:228059321:G:C
Gene:: WNT3A (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.228059322G>C, NC_000001.10:g.228247023G>C, NM_033131.4:c.916G>C, NM_033131.3:c.916G>C, NP_149122.1:p.Gly306Arg

Select item 145785728620.

rs1457857286 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:228059419 (GRCh38)
1:228247120 (GRCh37)
Canonical SPDI:: NC_000001.11:228059418:G:A
Gene:: WNT3A (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.228059419G>A, NC_000001.10:g.228247120G>A, NM_033131.4:c.1013G>A, NM_033131.3:c.1013G>A, NP_149122.1:p.Ser338Asn

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