SNP Links for Protein (Select 28274709) - SNP

Links from Protein

Items: 1 to 20 of 695

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Select item 14888346061.

rs1488834606 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:57909839 (GRCh38)
X:57936273 (GRCh37)
Canonical SPDI:: NC_000023.11:57909838:C:T
Gene:: ZXDA (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000023.11:g.57909839C>T, NC_000023.10:g.57936273C>T, NG_015974.1:g.5795G>A, NM_007156.4:c.582G>A, NM_007156.5:c.582G>A

Select item 14887168272.

rs1488716827 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: X:57909670 (GRCh38)
X:57936104 (GRCh37)
Canonical SPDI:: NC_000023.11:57909669:C:A
Gene:: ZXDA (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.00001/1 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000023.11:g.57909670C>A, NC_000023.10:g.57936104C>A, NG_015974.1:g.5964G>T, NM_007156.4:c.751G>T, NM_007156.5:c.751G>T, NP_009087.1:p.Ala251Ser

Select item 14883818463.

rs1488381846 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: X:57908056 (GRCh38)
X:57934490 (GRCh37)
Canonical SPDI:: NC_000023.11:57908055:G:C
Gene:: ZXDA (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
G=0./0 (SGDP_PRJ)
C=0.000006/1 (GnomAD_exomes)
C=0.000015/4 (TOPMED)
C=0.000019/2 (GnomAD)
HGVS:: NC_000023.11:g.57908056G>C, NC_000023.10:g.57934490G>C, NG_015974.1:g.7578C>G, NM_007156.4:c.2365C>G, NM_007156.5:c.2365C>G, NP_009087.1:p.Leu789Val

Select item 14883497954.

rs1488349795 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:57909148 (GRCh38)
X:57935582 (GRCh37)
Canonical SPDI:: NC_000023.11:57909147:G:A
Gene:: ZXDA (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000011/2 (GnomAD_exomes)
HGVS:: NC_000023.11:g.57909148G>A, NC_000023.10:g.57935582G>A, NG_015974.1:g.6486C>T, NM_007156.4:c.1273C>T, NM_007156.5:c.1273C>T, NP_009087.1:p.Pro425Ser

Select item 14874753765.

rs1487475376 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:57909009 (GRCh38)
X:57935443 (GRCh37)
Canonical SPDI:: NC_000023.11:57909008:T:C
Gene:: ZXDA (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=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.57909009T>C, NC_000023.10:g.57935443T>C, NG_015974.1:g.6625A>G, NM_007156.4:c.1412A>G, NM_007156.5:c.1412A>G, NP_009087.1:p.Lys471Arg

Select item 14854579356.

rs1485457935 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:57910410 (GRCh38)
X:57936844 (GRCh37)
Canonical SPDI:: NC_000023.11:57910409:G:A
Gene:: ZXDA (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.57910410G>A, NC_000023.10:g.57936844G>A, NG_015974.1:g.5224C>T, NM_007156.4:c.11C>T, NM_007156.5:c.11C>T, NP_009087.1:p.Pro4Leu

Select item 14846021597.

rs1484602159 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:57908048 (GRCh38)
X:57934482 (GRCh37)
Canonical SPDI:: NC_000023.11:57908047:A:G
Gene:: ZXDA (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.57908048A>G, NC_000023.10:g.57934482A>G, NG_015974.1:g.7586T>C, NM_007156.4:c.2373T>C, NM_007156.5:c.2373T>C

Select item 14842382598.

rs1484238259 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:57909380 (GRCh38)
X:57935814 (GRCh37)
Canonical SPDI:: NC_000023.11:57909379:G:A
Gene:: ZXDA (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=0.000019/2 (GnomAD)
HGVS:: NC_000023.11:g.57909380G>A, NC_000023.10:g.57935814G>A, NG_015974.1:g.6254C>T, NM_007156.4:c.1041C>T, NM_007156.5:c.1041C>T

Select item 14826953669.

rs1482695366 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: X:57908375 (GRCh38)
X:57934809 (GRCh37)
Canonical SPDI:: NC_000023.11:57908374:A:C
Gene:: ZXDA (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: C=0.000018/2 (GnomAD_exomes)
HGVS:: NC_000023.11:g.57908375A>C, NC_000023.10:g.57934809A>C, NG_015974.1:g.7259T>G, NM_007156.4:c.2046T>G, NM_007156.5:c.2046T>G

Select item 148228483210.

rs1482284832 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:57908146 (GRCh38)
X:57934580 (GRCh37)
Canonical SPDI:: NC_000023.11:57908145:G:A
Gene:: ZXDA (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.00001/1 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000023.11:g.57908146G>A, NC_000023.10:g.57934580G>A, NG_015974.1:g.7488C>T, NM_007156.4:c.2275C>T, NM_007156.5:c.2275C>T, NP_009087.1:p.Pro759Ser

Select item 148153091411.

rs1481530914 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:57908482 (GRCh38)
X:57934916 (GRCh37)
Canonical SPDI:: NC_000023.11:57908481:T:C
Gene:: ZXDA (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.57908482T>C, NC_000023.10:g.57934916T>C, NG_015974.1:g.7152A>G, NM_007156.4:c.1939A>G, NM_007156.5:c.1939A>G, NP_009087.1:p.Asn647Asp

Select item 148089940312.

rs1480899403 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:57908446 (GRCh38)
X:57934880 (GRCh37)
Canonical SPDI:: NC_000023.11:57908445:G:A
Gene:: ZXDA (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000023.11:g.57908446G>A, NC_000023.10:g.57934880G>A, NG_015974.1:g.7188C>T, NM_007156.4:c.1975C>T, NM_007156.5:c.1975C>T, NP_009087.1:p.Pro659Ser

Select item 147833343813.

rs1478333438 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: X:57910214 (GRCh38)
X:57936648 (GRCh37)
Canonical SPDI:: NC_000023.11:57910213:A:C,NC_000023.11:57910213:A:G
Gene:: ZXDA (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000015/4 (TOPMED)
G=0.000045/1 (TOMMO)
HGVS:: NC_000023.11:g.57910214A>C, NC_000023.11:g.57910214A>G, NC_000023.10:g.57936648A>C, NC_000023.10:g.57936648A>G, NG_015974.1:g.5420T>G, NG_015974.1:g.5420T>C, NM_007156.4:c.207T>G, NM_007156.4:c.207T>C, NM_007156.5:c.207T>G, NM_007156.5:c.207T>C

Select item 147644887114.

rs1476448871 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: X:57908850 (GRCh38)
X:57935284 (GRCh37)
Canonical SPDI:: NC_000023.11:57908849:C:A,NC_000023.11:57908849:C:G,NC_000023.11:57908849:C:T
Gene:: ZXDA (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
T=0.00021/1 (1000Genomes)
HGVS:: NC_000023.11:g.57908850C>A, NC_000023.11:g.57908850C>G, NC_000023.11:g.57908850C>T, NC_000023.10:g.57935284C>A, NC_000023.10:g.57935284C>G, NC_000023.10:g.57935284C>T, NG_015974.1:g.6784G>T, NG_015974.1:g.6784G>C, NG_015974.1:g.6784G>A, NM_007156.4:c.1571G>T, NM_007156.4:c.1571G>C, NM_007156.4:c.1571G>A, NM_007156.5:c.1571G>T, NM_007156.5:c.1571G>C, NM_007156.5:c.1571G>A, NP_009087.1:p.Arg524Leu, NP_009087.1:p.Arg524Pro, NP_009087.1:p.Arg524His

Select item 147637749215.

rs1476377492 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:57909688 (GRCh38)
X:57936122 (GRCh37)
Canonical SPDI:: NC_000023.11:57909687:C:T
Gene:: ZXDA (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000023.11:g.57909688C>T, NC_000023.10:g.57936122C>T, NG_015974.1:g.5946G>A, NM_007156.4:c.733G>A, NM_007156.5:c.733G>A, NP_009087.1:p.Ala245Thr

Select item 147534761416.

rs1475347614 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: X:57910162 (GRCh38)
X:57936596 (GRCh37)
Canonical SPDI:: NC_000023.11:57910161:C:A,NC_000023.11:57910161:C:T
Gene:: ZXDA (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
T=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.57910162C>A, NC_000023.11:g.57910162C>T, NC_000023.10:g.57936596C>A, NC_000023.10:g.57936596C>T, NG_015974.1:g.5472G>T, NG_015974.1:g.5472G>A, NM_007156.4:c.259G>T, NM_007156.4:c.259G>A, NM_007156.5:c.259G>T, NM_007156.5:c.259G>A, NP_009087.1:p.Asp87Tyr, NP_009087.1:p.Asp87Asn

Select item 147433055517.

rs1474330555 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:57910382 (GRCh38)
X:57936816 (GRCh37)
Canonical SPDI:: NC_000023.11:57910381:T:C
Gene:: ZXDA (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.57910382T>C, NC_000023.10:g.57936816T>C, NG_015974.1:g.5252A>G, NM_007156.4:c.39A>G, NM_007156.5:c.39A>G

Select item 147220085018.

rs1472200850 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:57908297 (GRCh38)
X:57934731 (GRCh37)
Canonical SPDI:: NC_000023.11:57908296:C:T
Gene:: ZXDA (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.57908297C>T, NC_000023.10:g.57934731C>T, NG_015974.1:g.7337G>A, NM_007156.4:c.2124G>A, NM_007156.5:c.2124G>A

Select item 147180738419.

rs1471807384 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: X:57908934 (GRCh38)
X:57935368 (GRCh37)
Canonical SPDI:: NC_000023.11:57908933:T:G
Gene:: ZXDA (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000023.11:g.57908934T>G, NC_000023.10:g.57935368T>G, NG_015974.1:g.6700A>C, NM_007156.4:c.1487A>C, NM_007156.5:c.1487A>C, NP_009087.1:p.His496Pro

Select item 147069375420.

rs1470693754 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:57909252 (GRCh38)
X:57935686 (GRCh37)
Canonical SPDI:: NC_000023.11:57909251:T:C
Gene:: ZXDA (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_000023.11:g.57909252T>C, NC_000023.10:g.57935686T>C, NG_015974.1:g.6382A>G, NM_007156.4:c.1169A>G, NM_007156.5:c.1169A>G, NP_009087.1:p.Gln390Arg

dbSNP

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