SNP Links for Protein (Select 21314662) - SNP

Links from Protein

Items: 1 to 20 of 485

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Select item 14907805401.

rs1490780540 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 12:133155795 (GRCh38)
12:133732381 (GRCh37)
Canonical SPDI:: NC_000012.12:133155794:G:A,NC_000012.12:133155794:G:C
Gene:: ZNF10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_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)
C=0.000035/1 (TOMMO)
HGVS:: NC_000012.12:g.133155795G>A, NC_000012.12:g.133155795G>C, NC_000012.11:g.133732381G>A, NC_000012.11:g.133732381G>C, NM_015394.5:c.549G>A, NM_015394.5:c.549G>C, NM_015394.4:c.549G>A, NM_015394.4:c.549G>C, NP_056209.2:p.Glu183Asp

Select item 14901871562.

rs1490187156 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 12:133151885 (GRCh38)
12:133728471 (GRCh37)
Canonical SPDI:: NC_000012.12:133151884:T:C
Gene:: ZNF10 (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_000012.12:g.133151885T>C, NC_000012.11:g.133728471T>C, NM_015394.5:c.237T>C, NM_015394.4:c.237T>C

Select item 14863132653.

rs1486313265 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 12:133156075 (GRCh38)
12:133732661 (GRCh37)
Canonical SPDI:: NC_000012.12:133156074:C:A,NC_000012.12:133156074:C:T
Gene:: ZNF10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000015/4 (TOPMED)
HGVS:: NC_000012.12:g.133156075C>A, NC_000012.12:g.133156075C>T, NC_000012.11:g.133732661C>A, NC_000012.11:g.133732661C>T, NM_015394.5:c.829C>A, NM_015394.5:c.829C>T, NM_015394.4:c.829C>A, NM_015394.4:c.829C>T, NP_056209.2:p.Arg277Ser, NP_056209.2:p.Arg277Cys

Select item 14848696824.

rs1484869682 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 12:133156777 (GRCh38)
12:133733363 (GRCh37)
Canonical SPDI:: NC_000012.12:133156776:C:G
Gene:: ZNF10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000142/2 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000012.12:g.133156777C>G, NC_000012.11:g.133733363C>G, NM_015394.5:c.1531C>G, NM_015394.4:c.1531C>G, NP_056209.2:p.His511Asp

Select item 14847971075.

rs1484797107 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 12:133151129 (GRCh38)
12:133727715 (GRCh37)
Canonical SPDI:: NC_000012.12:133151128:G:A
Gene:: ZNF10 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000012.12:g.133151129G>A, NC_000012.11:g.133727715G>A, NM_015394.5:c.135G>A, NM_015394.4:c.135G>A

Select item 14827491396.

rs1482749139 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:133156517 (GRCh38)
12:133733103 (GRCh37)
Canonical SPDI:: NC_000012.12:133156516:A:G
Gene:: ZNF10 (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=0.000007/1 (GnomAD)
HGVS:: NC_000012.12:g.133156517A>G, NC_000012.11:g.133733103A>G, NM_015394.5:c.1271A>G, NM_015394.4:c.1271A>G, NP_056209.2:p.His424Arg

Select item 14822852877.

rs1482285287 [Homo sapiens]

Variant type:: DELINS
Alleles:: GAGA>- [Show Flanks]
Chromosome:: 12:133151878 (GRCh38)
12:133728464 (GRCh37)
Canonical SPDI:: NC_000012.12:133151873:GAGAGAGA:GAGA
Gene:: ZNF10 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency
MAF:: -=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.133151874GA[2], NC_000012.11:g.133728460GA[2], NM_015394.5:c.230_233del, NM_015394.4:c.230_233del, NP_056209.2:p.Arg77fs

Select item 14813587658.

rs1481358765 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:133156637 (GRCh38)
12:133733223 (GRCh37)
Canonical SPDI:: NC_000012.12:133156636:A:G
Gene:: ZNF10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (GnomAD_exomes)
G=0.000008/2 (TOPMED)
HGVS:: NC_000012.12:g.133156637A>G, NC_000012.11:g.133733223A>G, NM_015394.5:c.1391A>G, NM_015394.4:c.1391A>G, NP_056209.2:p.His464Arg

Select item 14812672919.

rs1481267291 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:133155722 (GRCh38)
12:133732308 (GRCh37)
Canonical SPDI:: NC_000012.12:133155721:C:T
Gene:: ZNF10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.133155722C>T, NC_000012.11:g.133732308C>T, NM_015394.5:c.476C>T, NM_015394.4:c.476C>T, NP_056209.2:p.Thr159Ile

Select item 147386807410.

rs1473868074 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:133155960 (GRCh38)
12:133732546 (GRCh37)
Canonical SPDI:: NC_000012.12:133155959:C:T
Gene:: ZNF10 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000012.12:g.133155960C>T, NC_000012.11:g.133732546C>T, NM_015394.5:c.714C>T, NM_015394.4:c.714C>T

Select item 147385042411.

rs1473850424 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 12:133151890 (GRCh38)
12:133728476 (GRCh37)
Canonical SPDI:: NC_000012.12:133151889:A:C
Gene:: ZNF10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.133151890A>C, NC_000012.11:g.133728476A>C, NM_015394.5:c.242A>C, NM_015394.4:c.242A>C, NP_056209.2:p.Gln81Pro

Select item 147263846412.

rs1472638464 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 12:133156499 (GRCh38)
12:133733085 (GRCh37)
Canonical SPDI:: NC_000012.12:133156498:C:G
Gene:: ZNF10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000012.12:g.133156499C>G, NC_000012.11:g.133733085C>G, NM_015394.5:c.1253C>G, NM_015394.4:c.1253C>G, NP_056209.2:p.Ser418Cys

Select item 147188035113.

rs1471880351 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:133156206 (GRCh38)
12:133732792 (GRCh37)
Canonical SPDI:: NC_000012.12:133156205:C:T
Gene:: ZNF10 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.133156206C>T, NC_000012.11:g.133732792C>T, NM_015394.5:c.960C>T, NM_015394.4:c.960C>T

Select item 146595118414.

rs1465951184 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:133156015 (GRCh38)
12:133732601 (GRCh37)
Canonical SPDI:: NC_000012.12:133156014:A:G
Gene:: ZNF10 (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=0.000007/1 (GnomAD)
G=0.000011/3 (TOPMED)
HGVS:: NC_000012.12:g.133156015A>G, NC_000012.11:g.133732601A>G, NM_015394.5:c.769A>G, NM_015394.4:c.769A>G, NP_056209.2:p.Lys257Glu

Select item 146428105315.

rs1464281053 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CTT [Show Flanks]
Chromosome:: 12:133155983 (GRCh38)
12:133732570 (GRCh37)
Canonical SPDI:: NC_000012.12:133155983:TCTT:TCTTCTT
Gene:: ZNF10 (Varview)
Functional Consequence:: coding_sequence_variant,inframe_insertion
Validated:: by frequency,by alfa,by cluster
MAF:: TCTTCTT=0./0 (ALFA)
TCT=0.000004/1 (GnomAD_exomes)
TCT=0.000007/1 (GnomAD)
TCT=0.000008/2 (TOPMED)
HGVS:: NC_000012.12:g.133155985_133155987dup, NC_000012.11:g.133732571_133732573dup, NM_015394.5:c.739_741dup, NM_015394.4:c.739_741dup, NP_056209.2:p.Leu247dup

Select item 146292666116.

rs1462926661 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 12:133156894 (GRCh38)
12:133733480 (GRCh37)
Canonical SPDI:: NC_000012.12:133156893:T:C
Gene:: ZNF10 (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=0.000006/1 (GnomAD_exomes)
C=0.000014/2 (GnomAD)
HGVS:: NC_000012.12:g.133156894T>C, NC_000012.11:g.133733480T>C, NM_015394.5:c.1648T>C, NM_015394.4:c.1648T>C, NP_056209.2:p.Cys550Arg

Select item 146279986317.

rs1462799863 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 12:133156945 (GRCh38)
12:133733531 (GRCh37)
Canonical SPDI:: NC_000012.12:133156944:C:A
Gene:: ZNF10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000012.12:g.133156945C>A, NC_000012.11:g.133733531C>A, NM_015394.5:c.1699C>A, NM_015394.4:c.1699C>A, NP_056209.2:p.His567Asn

Select item 146278061518.

rs1462780615 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 12:133155951 (GRCh38)
12:133732537 (GRCh37)
Canonical SPDI:: NC_000012.12:133155950:T:G
Gene:: ZNF10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000028/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
HGVS:: NC_000012.12:g.133155951T>G, NC_000012.11:g.133732537T>G, NM_015394.5:c.705T>G, NM_015394.4:c.705T>G, NP_056209.2:p.Asp235Glu

Select item 145776571019.

rs1457765710 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 12:133156638 (GRCh38)
12:133733224 (GRCh37)
Canonical SPDI:: NC_000012.12:133156637:T:G
Gene:: ZNF10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000012.12:g.133156638T>G, NC_000012.11:g.133733224T>G, NM_015394.5:c.1392T>G, NM_015394.4:c.1392T>G, NP_056209.2:p.His464Gln

Select item 145309555220.

rs1453095552 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:133156661 (GRCh38)
12:133733247 (GRCh37)
Canonical SPDI:: NC_000012.12:133156660:A:G
Gene:: ZNF10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.133156661A>G, NC_000012.11:g.133733247A>G, NM_015394.5:c.1415A>G, NM_015394.4:c.1415A>G, NP_056209.2:p.Gln472Arg

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