SNP Links for Protein (Select 968121909) - SNP

Links from Protein

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Select item 14882838001.

rs1488283800 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:9529624 (GRCh38)
19:9640300 (GRCh37)
Canonical SPDI:: NC_000019.10:9529623:T:C
Gene:: ZNF426 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.9529624T>C, NC_000019.9:g.9640300T>C, NM_001300883.3:c.307A>G, NM_001300883.2:c.307A>G, NM_001300883.1:c.307A>G, NM_024106.3:c.421A>G, NM_024106.2:c.421A>G, NM_024106.1:c.421A>G, NM_001318056.2:c.338A>G, NM_001318056.1:c.338A>G, NM_001318055.2:c.88A>G, NM_001318055.1:c.88A>G, NP_001287812.1:p.Asn103Asp, NP_077011.1:p.Asn141Asp, NP_001304985.1:p.Gln113Arg, NP_001304984.1:p.Asn30Asp

Select item 14733417662.

rs1473341766 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:9533866 (GRCh38)
19:9644542 (GRCh37)
Canonical SPDI:: NC_000019.10:9533865:T:C
Gene:: ZNF426 (Varview)
Functional Consequence:: missense_variant,intron_variant,coding_sequence_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_000019.10:g.9533866T>C, NC_000019.9:g.9644542T>C, NM_001300883.3:c.104A>G, NM_001300883.2:c.104A>G, NM_001300883.1:c.104A>G, NM_024106.3:c.218A>G, NM_024106.2:c.218A>G, NM_024106.1:c.218A>G, NM_001318056.2:c.218A>G, NM_001318056.1:c.218A>G, NP_001287812.1:p.Glu35Gly, NP_077011.1:p.Glu73Gly, NP_001304985.1:p.Glu73Gly

Select item 14625863313.

rs1462586331 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 19:9533906 (GRCh38)
19:9644582 (GRCh37)
Canonical SPDI:: NC_000019.10:9533905:C:A
Gene:: ZNF426 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.9533906C>A, NC_000019.9:g.9644582C>A, NM_001300883.3:c.64G>T, NM_001300883.2:c.64G>T, NM_001300883.1:c.64G>T, NM_024106.3:c.178G>T, NM_024106.2:c.178G>T, NM_024106.1:c.178G>T, NM_001318056.2:c.178G>T, NM_001318056.1:c.178G>T, NP_001287812.1:p.Asp22Tyr, NP_077011.1:p.Asp60Tyr, NP_001304985.1:p.Asp60Tyr

Select item 14622212914.

rs1462221291 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 19:9532923 (GRCh38)
19:9643599 (GRCh37)
Canonical SPDI:: NC_000019.10:9532922:C:G
Gene:: ZNF426 (Varview)
Functional Consequence:: 5_prime_UTR_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000011/3 (TOPMED)
HGVS:: NC_000019.10:g.9532923C>G, NC_000019.9:g.9643599C>G, NM_001300883.3:c.133G>C, NM_001300883.2:c.133G>C, NM_001300883.1:c.133G>C, NM_024106.3:c.247G>C, NM_024106.2:c.247G>C, NM_024106.1:c.247G>C, NM_001318056.2:c.247G>C, NM_001318056.1:c.247G>C, NM_001318055.2:c.-87G>C, NM_001318055.1:c.-87G>C, NP_001287812.1:p.Gly45Arg, NP_077011.1:p.Gly83Arg, NP_001304985.1:p.Gly83Arg

Select item 14528192125.

rs1452819212 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 19:9533890 (GRCh38)
19:9644566 (GRCh37)
Canonical SPDI:: NC_000019.10:9533889:C:A
Gene:: ZNF426 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.9533890C>A, NC_000019.9:g.9644566C>A, NM_001300883.3:c.80G>T, NM_001300883.2:c.80G>T, NM_001300883.1:c.80G>T, NM_024106.3:c.194G>T, NM_024106.2:c.194G>T, NM_024106.1:c.194G>T, NM_001318056.2:c.194G>T, NM_001318056.1:c.194G>T, NP_001287812.1:p.Ser27Ile, NP_077011.1:p.Ser65Ile, NP_001304985.1:p.Ser65Ile

Select item 14465574876.

rs1446557487 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:9535200 (GRCh38)
19:9645876 (GRCh37)
Canonical SPDI:: NC_000019.10:9535199:T:C
Gene:: ZNF426 (Varview)
Functional Consequence:: intron_variant,5_prime_UTR_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000019.10:g.9535200T>C, NC_000019.9:g.9645876T>C, NM_024106.3:c.105A>G, NM_024106.2:c.105A>G, NM_024106.1:c.105A>G, NM_001318056.2:c.105A>G, NM_001318056.1:c.105A>G, NM_001318055.2:c.-102A>G, NM_001318055.1:c.-102A>G

Select item 14305104447.

rs1430510444 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:9536221 (GRCh38)
19:9646897 (GRCh37)
Canonical SPDI:: NC_000019.10:9536220:A:G
Gene:: ZNF426 (Varview)
Functional Consequence:: synonymous_variant,5_prime_UTR_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000011/3 (TOPMED)
HGVS:: NC_000019.10:g.9536221A>G, NC_000019.9:g.9646897A>G, NM_001300883.3:c.-11T>C, NM_001300883.2:c.-11T>C, NM_001300883.1:c.-11T>C, NM_024106.3:c.12T>C, NM_024106.2:c.12T>C, NM_024106.1:c.12T>C, NM_001318056.2:c.12T>C, NM_001318056.1:c.12T>C, NM_001318055.2:c.-195T>C, NM_001318055.1:c.-195T>C

Select item 14292092188.

rs1429209218 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:9532847 (GRCh38)
19:9643523 (GRCh37)
Canonical SPDI:: NC_000019.10:9532846:T:C
Gene:: ZNF426 (Varview)
Functional Consequence:: missense_variant,5_prime_UTR_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.9532847T>C, NC_000019.9:g.9643523T>C, NM_001300883.3:c.209A>G, NM_001300883.2:c.209A>G, NM_001300883.1:c.209A>G, NM_024106.3:c.323A>G, NM_024106.2:c.323A>G, NM_024106.1:c.323A>G, NM_001318056.2:c.323A>G, NM_001318056.1:c.323A>G, NM_001318055.2:c.-11A>G, NM_001318055.1:c.-11A>G, NP_001287812.1:p.Gln70Arg, NP_077011.1:p.Gln108Arg, NP_001304985.1:p.Gln108Arg

Select item 14263888859.

rs1426388885 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:9536210 (GRCh38)
19:9646886 (GRCh37)
Canonical SPDI:: NC_000019.10:9536209:T:C
Gene:: ZNF426 (Varview)
Functional Consequence:: initiator_codon_variant,missense_variant,5_prime_UTR_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (GnomAD_exomes)
C=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.9536210T>C, NC_000019.9:g.9646886T>C, NM_001300883.3:c.1A>G, NM_001300883.2:c.1A>G, NM_001300883.1:c.1A>G, NM_024106.3:c.23A>G, NM_024106.2:c.23A>G, NM_024106.1:c.23A>G, NM_001318056.2:c.23A>G, NM_001318056.1:c.23A>G, NM_001318055.2:c.-184A>G, NM_001318055.1:c.-184A>G, NP_001287812.1:p.Met1Val, NP_077011.1:p.His8Arg, NP_001304985.1:p.His8Arg

Select item 142631722410.

rs1426317224 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 19:9536215 (GRCh38)
19:9646891 (GRCh37)
Canonical SPDI:: NC_000019.10:9536214:C:A,NC_000019.10:9536214:C:T
Gene:: ZNF426 (Varview)
Functional Consequence:: synonymous_variant,missense_variant,5_prime_UTR_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
A=0.000035/1 (TOMMO)
HGVS:: NC_000019.10:g.9536215C>A, NC_000019.10:g.9536215C>T, NC_000019.9:g.9646891C>A, NC_000019.9:g.9646891C>T, NM_001300883.3:c.-5G>T, NM_001300883.3:c.-5G>A, NM_001300883.2:c.-5G>T, NM_001300883.2:c.-5G>A, NM_001300883.1:c.-5G>T, NM_001300883.1:c.-5G>A, NM_024106.3:c.18G>T, NM_024106.3:c.18G>A, NM_024106.2:c.18G>T, NM_024106.2:c.18G>A, NM_024106.1:c.18G>T, NM_024106.1:c.18G>A, NM_001318056.2:c.18G>T, NM_001318056.2:c.18G>A, NM_001318056.1:c.18G>T, NM_001318056.1:c.18G>A, NM_001318055.2:c.-189G>T, NM_001318055.2:c.-189G>A, NM_001318055.1:c.-189G>T, NM_001318055.1:c.-189G>A, NP_077011.1:p.Leu6Phe, NP_001304985.1:p.Leu6Phe

Select item 141643192111.

rs1416431921 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 19:9533955 (GRCh38)
19:9644631 (GRCh37)
Canonical SPDI:: NC_000019.10:9533954:G:C
Gene:: ZNF426 (Varview)
Functional Consequence:: intron_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000019.10:g.9533955G>C, NC_000019.9:g.9644631G>C, NM_001300883.3:c.15C>G, NM_001300883.2:c.15C>G, NM_001300883.1:c.15C>G, NM_024106.3:c.129C>G, NM_024106.2:c.129C>G, NM_024106.1:c.129C>G, NM_001318056.2:c.129C>G, NM_001318056.1:c.129C>G

Select item 141442658712.

rs1414426587 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:9533941 (GRCh38)
19:9644617 (GRCh37)
Canonical SPDI:: NC_000019.10:9533940:G:A
Gene:: ZNF426 (Varview)
Functional Consequence:: intron_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000019.10:g.9533941G>A, NC_000019.9:g.9644617G>A, NM_001300883.3:c.29C>T, NM_001300883.2:c.29C>T, NM_001300883.1:c.29C>T, NM_024106.3:c.143C>T, NM_024106.2:c.143C>T, NM_024106.1:c.143C>T, NM_001318056.2:c.143C>T, NM_001318056.1:c.143C>T, NP_001287812.1:p.Ala10Val, NP_077011.1:p.Ala48Val, NP_001304985.1:p.Ala48Val

Select item 141017424013.

rs1410174240 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:9533844 (GRCh38)
19:9644520 (GRCh37)
Canonical SPDI:: NC_000019.10:9533843:T:C
Gene:: ZNF426 (Varview)
Functional Consequence:: intron_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0.000084/1 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.9533844T>C, NC_000019.9:g.9644520T>C, NM_001300883.3:c.126A>G, NM_001300883.2:c.126A>G, NM_001300883.1:c.126A>G, NM_024106.3:c.240A>G, NM_024106.2:c.240A>G, NM_024106.1:c.240A>G, NM_001318056.2:c.240A>G, NM_001318056.1:c.240A>G

Select item 138744282114.

rs1387442821 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 19:9532873 (GRCh38)
19:9643549 (GRCh37)
Canonical SPDI:: NC_000019.10:9532872:T:G
Gene:: ZNF426 (Varview)
Functional Consequence:: synonymous_variant,5_prime_UTR_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000224/1 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000223/1 (Estonian)
HGVS:: NC_000019.10:g.9532873T>G, NC_000019.9:g.9643549T>G, NM_001300883.3:c.183A>C, NM_001300883.2:c.183A>C, NM_001300883.1:c.183A>C, NM_024106.3:c.297A>C, NM_024106.2:c.297A>C, NM_024106.1:c.297A>C, NM_001318056.2:c.297A>C, NM_001318056.1:c.297A>C, NM_001318055.2:c.-37A>C, NM_001318055.1:c.-37A>C

Select item 138666389215.

rs1386663892 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:9533945 (GRCh38)
19:9644621 (GRCh37)
Canonical SPDI:: NC_000019.10:9533944:C:T
Gene:: ZNF426 (Varview)
Functional Consequence:: intron_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000035/1 (TOMMO)
HGVS:: NC_000019.10:g.9533945C>T, NC_000019.9:g.9644621C>T, NM_001300883.3:c.25G>A, NM_001300883.2:c.25G>A, NM_001300883.1:c.25G>A, NM_024106.3:c.139G>A, NM_024106.2:c.139G>A, NM_024106.1:c.139G>A, NM_001318056.2:c.139G>A, NM_001318056.1:c.139G>A, NP_001287812.1:p.Val9Met, NP_077011.1:p.Val47Met, NP_001304985.1:p.Val47Met

Select item 138415335816.

rs1384153358 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 19:9532918 (GRCh38)
19:9643594 (GRCh37)
Canonical SPDI:: NC_000019.10:9532917:C:A
Gene:: ZNF426 (Varview)
Functional Consequence:: 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)
HGVS:: NC_000019.10:g.9532918C>A, NC_000019.9:g.9643594C>A, NM_001300883.3:c.138G>T, NM_001300883.2:c.138G>T, NM_001300883.1:c.138G>T, NM_024106.3:c.252G>T, NM_024106.2:c.252G>T, NM_024106.1:c.252G>T, NM_001318056.2:c.252G>T, NM_001318056.1:c.252G>T, NM_001318055.2:c.-82G>T, NM_001318055.1:c.-82G>T, NP_001287812.1:p.Gln46His, NP_077011.1:p.Gln84His, NP_001304985.1:p.Gln84His

Select item 137974635617.

rs1379746356 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:9535191 (GRCh38)
19:9645867 (GRCh37)
Canonical SPDI:: NC_000019.10:9535190:A:G
Gene:: ZNF426 (Varview)
Functional Consequence:: 5_prime_UTR_variant,intron_variant,synonymous_variant,coding_sequence_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_000019.10:g.9535191A>G, NC_000019.9:g.9645867A>G, NM_024106.3:c.114T>C, NM_024106.2:c.114T>C, NM_024106.1:c.114T>C, NM_001318056.2:c.114T>C, NM_001318056.1:c.114T>C, NM_001318055.2:c.-93T>C, NM_001318055.1:c.-93T>C

Select item 137920963018.

rs1379209630 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 19:9533958 (GRCh38)
19:9644634 (GRCh37)
Canonical SPDI:: NC_000019.10:9533957:C:A
Gene:: ZNF426 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,synonymous_variant
HGVS:: NC_000019.10:g.9533958C>A, NC_000019.9:g.9644634C>A, NM_001300883.3:c.12G>T, NM_001300883.2:c.12G>T, NM_001300883.1:c.12G>T, NM_024106.3:c.126G>T, NM_024106.2:c.126G>T, NM_024106.1:c.126G>T, NM_001318056.2:c.126G>T, NM_001318056.1:c.126G>T

Select item 136019839619.

rs1360198396 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:9529620 (GRCh38)
19:9640296 (GRCh37)
Canonical SPDI:: NC_000019.10:9529619:C:T
Gene:: ZNF426 (Varview)
Functional Consequence:: stop_gained,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000093/2 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000017/4 (GnomAD_exomes)
T=0.000223/1 (Estonian)
HGVS:: NC_000019.10:g.9529620C>T, NC_000019.9:g.9640296C>T, NM_001300883.3:c.311G>A, NM_001300883.2:c.311G>A, NM_001300883.1:c.311G>A, NM_024106.3:c.425G>A, NM_024106.2:c.425G>A, NM_024106.1:c.425G>A, NM_001318056.2:c.342G>A, NM_001318056.1:c.342G>A, NM_001318055.2:c.92G>A, NM_001318055.1:c.92G>A, NP_001287812.1:p.Gly104Glu, NP_077011.1:p.Gly142Glu, NP_001304985.1:p.Trp114Ter, NP_001304984.1:p.Gly31Glu

Select item 135443473420.

rs1354434734 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:9535259 (GRCh38)
19:9645935 (GRCh37)
Canonical SPDI:: NC_000019.10:9535258:G:A
Gene:: ZNF426 (Varview)
Functional Consequence:: 5_prime_UTR_variant,intron_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000367/6 (ALFA)
A=0.000029/4 (GnomAD)
A=0.001116/5 (Estonian)
HGVS:: NC_000019.10:g.9535259G>A, NC_000019.9:g.9645935G>A, NM_024106.3:c.46C>T, NM_024106.2:c.46C>T, NM_024106.1:c.46C>T, NM_001318056.2:c.46C>T, NM_001318056.1:c.46C>T, NM_001318055.2:c.-161C>T, NM_001318055.1:c.-161C>T, NP_077011.1:p.Pro16Ser, NP_001304985.1:p.Pro16Ser

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