SNP Links for Protein (Select 47933348) - SNP - NCBI

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Links from Protein

Items: 1 to 20 of 462

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Select item 14801873191.

rs1480187319 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 11:19152207 (GRCh38)
11:19173754 (GRCh37)
Canonical SPDI:: NC_000011.10:19152206:G:A,NC_000011.10:19152206:G:C
Gene:: ZDHHC13 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
C=0.000035/1 (TOMMO)
HGVS:: NC_000011.10:g.19152207G>A, NC_000011.10:g.19152207G>C, NC_000011.9:g.19173754G>A, NC_000011.9:g.19173754G>C, NM_019028.3:c.634G>A, NM_019028.3:c.634G>C, NM_019028.2:c.634G>A, NM_019028.2:c.634G>C, XM_005252996.3:c.244G>A, XM_005252996.3:c.244G>C, XM_005252996.2:c.244G>A, XM_005252996.2:c.244G>C, XM_005252996.1:c.244G>A, XM_005252996.1:c.244G>C, NM_001001483.3:c.244G>A, NM_001001483.3:c.244G>C, NM_001001483.2:c.244G>A, NM_001001483.2:c.244G>C, XM_011520194.3:c.694G>A, XM_011520194.3:c.694G>C, XM_011520194.2:c.694G>A, XM_011520194.2:c.694G>C, XM_011520194.1:c.694G>A, XM_011520194.1:c.694G>C, XM_011520195.2:c.244G>A, XM_011520195.2:c.244G>C, XM_011520195.1:c.244G>A, XM_011520195.1:c.244G>C, XM_047427139.1:c.610G>A, XM_047427139.1:c.610G>C, XM_047427138.1:c.694G>A, XM_047427138.1:c.694G>C, XM_047427141.1:c.634G>A, XM_047427141.1:c.634G>C, XM_047427142.1:c.244G>A, XM_047427142.1:c.244G>C, XM_047427140.1:c.694G>A, XM_047427140.1:c.694G>C, XM_047427143.1:c.244G>A, XM_047427143.1:c.244G>C, XM_047427144.1:c.694G>A, XM_047427144.1:c.694G>C, NP_061901.2:p.Val212Ile, NP_061901.2:p.Val212Leu, XP_005253053.1:p.Val82Ile, XP_005253053.1:p.Val82Leu, NP_001001483.1:p.Val82Ile, NP_001001483.1:p.Val82Leu, XP_011518496.1:p.Val232Ile, XP_011518496.1:p.Val232Leu, XP_011518497.1:p.Val82Ile, XP_011518497.1:p.Val82Leu, XP_047283095.1:p.Val204Ile, XP_047283095.1:p.Val204Leu, XP_047283094.1:p.Val232Ile, XP_047283094.1:p.Val232Leu, XP_047283097.1:p.Val212Ile, XP_047283097.1:p.Val212Leu, XP_047283098.1:p.Val82Ile, XP_047283098.1:p.Val82Leu, XP_047283096.1:p.Val232Ile, XP_047283096.1:p.Val232Leu, XP_047283099.1:p.Val82Ile, XP_047283099.1:p.Val82Leu, XP_047283100.1:p.Val232Ile, XP_047283100.1:p.Val232Leu

Select item 14780389062.

rs1478038906 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:19170439 (GRCh38)
11:19191986 (GRCh37)
Canonical SPDI:: NC_000011.10:19170438:C:T
Gene:: ZDHHC13 (Varview)
Functional Consequence:: 3_prime_UTR_variant,coding_sequence_variant,genic_downstream_transcript_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.00006/2 (ALFA)
T=0.000009/1 (GnomAD)
T=0.000028/4 (GnomAD_exomes)
HGVS:: NC_000011.10:g.19170439C>T, NC_000011.9:g.19191986C>T, NM_019028.3:c.1503C>T, NM_019028.2:c.1503C>T, XM_005252996.3:c.1113C>T, XM_005252996.2:c.1113C>T, XM_005252996.1:c.1113C>T, NM_001001483.3:c.1113C>T, NM_001001483.2:c.1113C>T, XM_011520194.3:c.*30C>T, XM_011520194.2:c.*30C>T, XM_011520194.1:c.*30C>T, XM_011520195.2:c.1113C>T, XM_011520195.1:c.1113C>T, XM_047427139.1:c.1479C>T, XM_047427138.1:c.1563C>T, XM_047427141.1:c.1419C>T, XM_047427142.1:c.1029C>T, XM_047427140.1:c.1479C>T, XM_047427143.1:c.1029C>T

Select item 14750076863.

rs1475007686 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:19155855 (GRCh38)
11:19177402 (GRCh37)
Canonical SPDI:: NC_000011.10:19155854:C:T
Gene:: ZDHHC13 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by cluster
MAF:: T=0.000004/1 (GnomAD_exomes)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.19155855C>T, NC_000011.9:g.19177402C>T, NM_019028.3:c.933C>T, NM_019028.2:c.933C>T, XM_005252996.3:c.543C>T, XM_005252996.2:c.543C>T, XM_005252996.1:c.543C>T, NM_001001483.3:c.543C>T, NM_001001483.2:c.543C>T, XM_011520194.3:c.993C>T, XM_011520194.2:c.993C>T, XM_011520194.1:c.993C>T, XM_011520195.2:c.543C>T, XM_011520195.1:c.543C>T, XM_047427139.1:c.909C>T, XM_047427138.1:c.993C>T, XM_047427141.1:c.933C>T, XM_047427142.1:c.543C>T, XM_047427140.1:c.993C>T, XM_047427143.1:c.543C>T, XM_047427144.1:c.993C>T

Select item 14726757074.

rs1472675707 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:19158980 (GRCh38)
11:19180527 (GRCh37)
Canonical SPDI:: NC_000011.10:19158979:G:A
Gene:: ZDHHC13 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.19158980G>A, NC_000011.9:g.19180527G>A, NM_019028.3:c.1048G>A, NM_019028.2:c.1048G>A, XM_005252996.3:c.658G>A, XM_005252996.2:c.658G>A, XM_005252996.1:c.658G>A, NM_001001483.3:c.658G>A, NM_001001483.2:c.658G>A, XM_011520194.3:c.1108G>A, XM_011520194.2:c.1108G>A, XM_011520194.1:c.1108G>A, XM_011520195.2:c.658G>A, XM_011520195.1:c.658G>A, XM_047427139.1:c.1024G>A, XM_047427138.1:c.1108G>A, XM_047427141.1:c.1048G>A, XM_047427142.1:c.658G>A, XM_047427140.1:c.1108G>A, XM_047427143.1:c.658G>A, NP_061901.2:p.Ala350Thr, XP_005253053.1:p.Ala220Thr, NP_001001483.1:p.Ala220Thr, XP_011518496.1:p.Ala370Thr, XP_011518497.1:p.Ala220Thr, XP_047283095.1:p.Ala342Thr, XP_047283094.1:p.Ala370Thr, XP_047283097.1:p.Ala350Thr, XP_047283098.1:p.Ala220Thr, XP_047283096.1:p.Ala370Thr, XP_047283099.1:p.Ala220Thr

Select item 14642032785.

rs1464203278 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:19172779 (GRCh38)
11:19194326 (GRCh37)
Canonical SPDI:: NC_000011.10:19172778:G:A
Gene:: ZDHHC13 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,genic_downstream_transcript_variant
HGVS:: NC_000011.10:g.19172779G>A, NC_000011.9:g.19194326G>A, NG_054100.1:g.343G>A, NM_019028.3:c.1689G>A, NM_019028.2:c.1689G>A, XM_005252996.3:c.1299G>A, XM_005252996.2:c.1299G>A, XM_005252996.1:c.1299G>A, NM_001001483.3:c.1299G>A, NM_001001483.2:c.1299G>A, XM_011520195.2:c.1299G>A, XM_011520195.1:c.1299G>A, XM_047427139.1:c.1665G>A, XM_047427138.1:c.1749G>A, XM_047427141.1:c.1605G>A, XM_047427142.1:c.1215G>A, XM_047427140.1:c.1665G>A, XM_047427143.1:c.1215G>A

Select item 14640080016.

rs1464008001 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:19152290 (GRCh38)
11:19173837 (GRCh37)
Canonical SPDI:: NC_000011.10:19152289:T:C
Gene:: ZDHHC13 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000011/3 (TOPMED)
HGVS:: NC_000011.10:g.19152290T>C, NC_000011.9:g.19173837T>C, NM_019028.3:c.717T>C, NM_019028.2:c.717T>C, XM_005252996.3:c.327T>C, XM_005252996.2:c.327T>C, XM_005252996.1:c.327T>C, NM_001001483.3:c.327T>C, NM_001001483.2:c.327T>C, XM_011520194.3:c.777T>C, XM_011520194.2:c.777T>C, XM_011520194.1:c.777T>C, XM_011520195.2:c.327T>C, XM_011520195.1:c.327T>C, XM_047427139.1:c.693T>C, XM_047427138.1:c.777T>C, XM_047427141.1:c.717T>C, XM_047427142.1:c.327T>C, XM_047427140.1:c.777T>C, XM_047427143.1:c.327T>C, XM_047427144.1:c.777T>C

Select item 14635521057.

rs1463552105 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 11:19164311 (GRCh38)
11:19185858 (GRCh37)
Canonical SPDI:: NC_000011.10:19164310:C:A,NC_000011.10:19164310:C:T
Gene:: ZDHHC13 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.00004/1 (TOMMO)
HGVS:: NC_000011.10:g.19164311C>A, NC_000011.10:g.19164311C>T, NC_000011.9:g.19185858C>A, NC_000011.9:g.19185858C>T, NM_019028.3:c.1244C>A, NM_019028.3:c.1244C>T, NM_019028.2:c.1244C>A, NM_019028.2:c.1244C>T, XM_005252996.3:c.854C>A, XM_005252996.3:c.854C>T, XM_005252996.2:c.854C>A, XM_005252996.2:c.854C>T, XM_005252996.1:c.854C>A, XM_005252996.1:c.854C>T, NM_001001483.3:c.854C>A, NM_001001483.3:c.854C>T, NM_001001483.2:c.854C>A, NM_001001483.2:c.854C>T, XM_011520194.3:c.1304C>A, XM_011520194.3:c.1304C>T, XM_011520194.2:c.1304C>A, XM_011520194.2:c.1304C>T, XM_011520194.1:c.1304C>A, XM_011520194.1:c.1304C>T, XM_011520195.2:c.854C>A, XM_011520195.2:c.854C>T, XM_011520195.1:c.854C>A, XM_011520195.1:c.854C>T, XM_047427139.1:c.1220C>A, XM_047427139.1:c.1220C>T, XM_047427138.1:c.1304C>A, XM_047427138.1:c.1304C>T, XM_047427141.1:c.1244C>A, XM_047427141.1:c.1244C>T, XM_047427142.1:c.854C>A, XM_047427142.1:c.854C>T, XM_047427140.1:c.1304C>A, XM_047427140.1:c.1304C>T, XM_047427143.1:c.854C>A, XM_047427143.1:c.854C>T, XM_047427144.1:c.1078C>A, XM_047427144.1:c.1078C>T, NP_061901.2:p.Thr415Asn, NP_061901.2:p.Thr415Ile, XP_005253053.1:p.Thr285Asn, XP_005253053.1:p.Thr285Ile, NP_001001483.1:p.Thr285Asn, NP_001001483.1:p.Thr285Ile, XP_011518496.1:p.Thr435Asn, XP_011518496.1:p.Thr435Ile, XP_011518497.1:p.Thr285Asn, XP_011518497.1:p.Thr285Ile, XP_047283095.1:p.Thr407Asn, XP_047283095.1:p.Thr407Ile, XP_047283094.1:p.Thr435Asn, XP_047283094.1:p.Thr435Ile, XP_047283097.1:p.Thr415Asn, XP_047283097.1:p.Thr415Ile, XP_047283098.1:p.Thr285Asn, XP_047283098.1:p.Thr285Ile, XP_047283096.1:p.Thr435Asn, XP_047283096.1:p.Thr435Ile, XP_047283099.1:p.Thr285Asn, XP_047283099.1:p.Thr285Ile, XP_047283100.1:p.Pro360Thr, XP_047283100.1:p.Pro360Ser

Select item 14622987718.

rs1462298771 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:19152220 (GRCh38)
11:19173767 (GRCh37)
Canonical SPDI:: NC_000011.10:19152219:A:C
Gene:: ZDHHC13 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.19152220A>C, NC_000011.9:g.19173767A>C, NM_019028.3:c.647A>C, NM_019028.2:c.647A>C, XM_005252996.3:c.257A>C, XM_005252996.2:c.257A>C, XM_005252996.1:c.257A>C, NM_001001483.3:c.257A>C, NM_001001483.2:c.257A>C, XM_011520194.3:c.707A>C, XM_011520194.2:c.707A>C, XM_011520194.1:c.707A>C, XM_011520195.2:c.257A>C, XM_011520195.1:c.257A>C, XM_047427139.1:c.623A>C, XM_047427138.1:c.707A>C, XM_047427141.1:c.647A>C, XM_047427142.1:c.257A>C, XM_047427140.1:c.707A>C, XM_047427143.1:c.257A>C, XM_047427144.1:c.707A>C, NP_061901.2:p.His216Pro, XP_005253053.1:p.His86Pro, NP_001001483.1:p.His86Pro, XP_011518496.1:p.His236Pro, XP_011518497.1:p.His86Pro, XP_047283095.1:p.His208Pro, XP_047283094.1:p.His236Pro, XP_047283097.1:p.His216Pro, XP_047283098.1:p.His86Pro, XP_047283096.1:p.His236Pro, XP_047283099.1:p.His86Pro, XP_047283100.1:p.His236Pro

Select item 14621338999.

rs1462133899 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:19158990 (GRCh38)
11:19180537 (GRCh37)
Canonical SPDI:: NC_000011.10:19158989:T:C
Gene:: ZDHHC13 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_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_000011.10:g.19158990T>C, NC_000011.9:g.19180537T>C, NM_019028.3:c.1058T>C, NM_019028.2:c.1058T>C, XM_005252996.3:c.668T>C, XM_005252996.2:c.668T>C, XM_005252996.1:c.668T>C, NM_001001483.3:c.668T>C, NM_001001483.2:c.668T>C, XM_011520194.3:c.1118T>C, XM_011520194.2:c.1118T>C, XM_011520194.1:c.1118T>C, XM_011520195.2:c.668T>C, XM_011520195.1:c.668T>C, XM_047427139.1:c.1034T>C, XM_047427138.1:c.1118T>C, XM_047427141.1:c.1058T>C, XM_047427142.1:c.668T>C, XM_047427140.1:c.1118T>C, XM_047427143.1:c.668T>C, NP_061901.2:p.Leu353Pro, XP_005253053.1:p.Leu223Pro, NP_001001483.1:p.Leu223Pro, XP_011518496.1:p.Leu373Pro, XP_011518497.1:p.Leu223Pro, XP_047283095.1:p.Leu345Pro, XP_047283094.1:p.Leu373Pro, XP_047283097.1:p.Leu353Pro, XP_047283098.1:p.Leu223Pro, XP_047283096.1:p.Leu373Pro, XP_047283099.1:p.Leu223Pro

Select item 146171169010.

rs1461711690 [Homo sapiens]

Variant type:: DELINS
Alleles:: G>- [Show Flanks]
Chromosome:: 11:19170568 (GRCh38)
11:19192115 (GRCh37)
Canonical SPDI:: NC_000011.10:19170567:GG:G
Gene:: ZDHHC13 (Varview)
Functional Consequence:: coding_sequence_variant,downstream_transcript_variant,splice_donor_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GG=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.19170569del, NC_000011.9:g.19192116del

Select item 146077838411.

rs1460778384 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:19149287 (GRCh38)
11:19170834 (GRCh37)
Canonical SPDI:: NC_000011.10:19149286:T:C
Gene:: ZDHHC13 (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=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.19149287T>C, NC_000011.9:g.19170834T>C, NM_019028.3:c.475T>C, NM_019028.2:c.475T>C, XM_005252996.3:c.85T>C, XM_005252996.2:c.85T>C, XM_005252996.1:c.85T>C, NM_001001483.3:c.85T>C, NM_001001483.2:c.85T>C, XM_011520194.3:c.535T>C, XM_011520194.2:c.535T>C, XM_011520194.1:c.535T>C, XM_011520195.2:c.85T>C, XM_011520195.1:c.85T>C, XM_047427139.1:c.451T>C, XM_047427138.1:c.535T>C, XM_047427141.1:c.475T>C, XM_047427142.1:c.85T>C, XM_047427140.1:c.535T>C, XM_047427143.1:c.85T>C, XM_047427144.1:c.535T>C, NP_061901.2:p.Phe159Leu, XP_005253053.1:p.Phe29Leu, NP_001001483.1:p.Phe29Leu, XP_011518496.1:p.Phe179Leu, XP_011518497.1:p.Phe29Leu, XP_047283095.1:p.Phe151Leu, XP_047283094.1:p.Phe179Leu, XP_047283097.1:p.Phe159Leu, XP_047283098.1:p.Phe29Leu, XP_047283096.1:p.Phe179Leu, XP_047283099.1:p.Phe29Leu, XP_047283100.1:p.Phe179Leu

Select item 145885910712.

rs1458859107 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 11:19165076 (GRCh38)
11:19186623 (GRCh37)
Canonical SPDI:: NC_000011.10:19165075:C:A,NC_000011.10:19165075:C:T
Gene:: ZDHHC13 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
A=0.000016/4 (GnomAD_exomes)
HGVS:: NC_000011.10:g.19165076C>A, NC_000011.10:g.19165076C>T, NC_000011.9:g.19186623C>A, NC_000011.9:g.19186623C>T, NM_019028.3:c.1321C>A, NM_019028.3:c.1321C>T, NM_019028.2:c.1321C>A, NM_019028.2:c.1321C>T, XM_005252996.3:c.931C>A, XM_005252996.3:c.931C>T, XM_005252996.2:c.931C>A, XM_005252996.2:c.931C>T, XM_005252996.1:c.931C>A, XM_005252996.1:c.931C>T, NM_001001483.3:c.931C>A, NM_001001483.3:c.931C>T, NM_001001483.2:c.931C>A, NM_001001483.2:c.931C>T, XM_011520194.3:c.1381C>A, XM_011520194.3:c.1381C>T, XM_011520194.2:c.1381C>A, XM_011520194.2:c.1381C>T, XM_011520194.1:c.1381C>A, XM_011520194.1:c.1381C>T, XM_011520195.2:c.931C>A, XM_011520195.2:c.931C>T, XM_011520195.1:c.931C>A, XM_011520195.1:c.931C>T, XM_047427139.1:c.1297C>A, XM_047427139.1:c.1297C>T, XM_047427138.1:c.1381C>A, XM_047427138.1:c.1381C>T, XM_047427141.1:c.1321C>A, XM_047427141.1:c.1321C>T, XM_047427142.1:c.931C>A, XM_047427142.1:c.931C>T, XM_047427140.1:c.1381C>A, XM_047427140.1:c.1381C>T, XM_047427143.1:c.931C>A, XM_047427143.1:c.931C>T, XM_047427144.1:c.*21C>A, XM_047427144.1:c.*21C>T, NP_061901.2:p.His441Asn, NP_061901.2:p.His441Tyr, XP_005253053.1:p.His311Asn, XP_005253053.1:p.His311Tyr, NP_001001483.1:p.His311Asn, NP_001001483.1:p.His311Tyr, XP_011518496.1:p.His461Asn, XP_011518496.1:p.His461Tyr, XP_011518497.1:p.His311Asn, XP_011518497.1:p.His311Tyr, XP_047283095.1:p.His433Asn, XP_047283095.1:p.His433Tyr, XP_047283094.1:p.His461Asn, XP_047283094.1:p.His461Tyr, XP_047283097.1:p.His441Asn, XP_047283097.1:p.His441Tyr, XP_047283098.1:p.His311Asn, XP_047283098.1:p.His311Tyr, XP_047283096.1:p.His461Asn, XP_047283096.1:p.His461Tyr, XP_047283099.1:p.His311Asn, XP_047283099.1:p.His311Tyr

Select item 145873354213.

rs1458733542 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 11:19172752 (GRCh38)
11:19194299 (GRCh37)
Canonical SPDI:: NC_000011.10:19172751:G:A,NC_000011.10:19172751:G:C
Gene:: ZDHHC13 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,missense_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
A=0.000009/2 (GnomAD_exomes)
HGVS:: NC_000011.10:g.19172752G>A, NC_000011.10:g.19172752G>C, NC_000011.9:g.19194299G>A, NC_000011.9:g.19194299G>C, NG_054100.1:g.316G>A, NG_054100.1:g.316G>C, NM_019028.3:c.1662G>A, NM_019028.3:c.1662G>C, NM_019028.2:c.1662G>A, NM_019028.2:c.1662G>C, XM_005252996.3:c.1272G>A, XM_005252996.3:c.1272G>C, XM_005252996.2:c.1272G>A, XM_005252996.2:c.1272G>C, XM_005252996.1:c.1272G>A, XM_005252996.1:c.1272G>C, NM_001001483.3:c.1272G>A, NM_001001483.3:c.1272G>C, NM_001001483.2:c.1272G>A, NM_001001483.2:c.1272G>C, XM_011520195.2:c.1272G>A, XM_011520195.2:c.1272G>C, XM_011520195.1:c.1272G>A, XM_011520195.1:c.1272G>C, XM_047427139.1:c.1638G>A, XM_047427139.1:c.1638G>C, XM_047427138.1:c.1722G>A, XM_047427138.1:c.1722G>C, XM_047427141.1:c.1578G>A, XM_047427141.1:c.1578G>C, XM_047427142.1:c.1188G>A, XM_047427142.1:c.1188G>C, XM_047427140.1:c.1638G>A, XM_047427140.1:c.1638G>C, XM_047427143.1:c.1188G>A, XM_047427143.1:c.1188G>C, NP_061901.2:p.Glu554Asp, XP_005253053.1:p.Glu424Asp, NP_001001483.1:p.Glu424Asp, XP_011518497.1:p.Glu424Asp, XP_047283095.1:p.Glu546Asp, XP_047283094.1:p.Glu574Asp, XP_047283097.1:p.Glu526Asp, XP_047283098.1:p.Glu396Asp, XP_047283096.1:p.Glu546Asp, XP_047283099.1:p.Glu396Asp

Select item 145773229414.

rs1457732294 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 11:19170411 (GRCh38)
11:19191958 (GRCh37)
Canonical SPDI:: NC_000011.10:19170410:A:G,NC_000011.10:19170410:A:T
Gene:: ZDHHC13 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
T=0.00014/4 (TOMMO)
HGVS:: NC_000011.10:g.19170411A>G, NC_000011.10:g.19170411A>T, NC_000011.9:g.19191958A>G, NC_000011.9:g.19191958A>T, NM_019028.3:c.1475A>G, NM_019028.3:c.1475A>T, NM_019028.2:c.1475A>G, NM_019028.2:c.1475A>T, XM_005252996.3:c.1085A>G, XM_005252996.3:c.1085A>T, XM_005252996.2:c.1085A>G, XM_005252996.2:c.1085A>T, XM_005252996.1:c.1085A>G, XM_005252996.1:c.1085A>T, NM_001001483.3:c.1085A>G, NM_001001483.3:c.1085A>T, NM_001001483.2:c.1085A>G, NM_001001483.2:c.1085A>T, XM_011520194.3:c.*2A>G, XM_011520194.3:c.*2A>T, XM_011520194.2:c.*2A>G, XM_011520194.2:c.*2A>T, XM_011520194.1:c.*2A>G, XM_011520194.1:c.*2A>T, XM_011520195.2:c.1085A>G, XM_011520195.2:c.1085A>T, XM_011520195.1:c.1085A>G, XM_011520195.1:c.1085A>T, XM_047427139.1:c.1451A>G, XM_047427139.1:c.1451A>T, XM_047427138.1:c.1535A>G, XM_047427138.1:c.1535A>T, XM_047427141.1:c.1391A>G, XM_047427141.1:c.1391A>T, XM_047427142.1:c.1001A>G, XM_047427142.1:c.1001A>T, XM_047427140.1:c.1451A>G, XM_047427140.1:c.1451A>T, XM_047427143.1:c.1001A>G, XM_047427143.1:c.1001A>T, NP_061901.2:p.Tyr492Cys, NP_061901.2:p.Tyr492Phe, XP_005253053.1:p.Tyr362Cys, XP_005253053.1:p.Tyr362Phe, NP_001001483.1:p.Tyr362Cys, NP_001001483.1:p.Tyr362Phe, XP_011518497.1:p.Tyr362Cys, XP_011518497.1:p.Tyr362Phe, XP_047283095.1:p.Tyr484Cys, XP_047283095.1:p.Tyr484Phe, XP_047283094.1:p.Tyr512Cys, XP_047283094.1:p.Tyr512Phe, XP_047283097.1:p.Asp464Gly, XP_047283097.1:p.Asp464Val, XP_047283098.1:p.Asp334Gly, XP_047283098.1:p.Asp334Val, XP_047283096.1:p.Asp484Gly, XP_047283096.1:p.Asp484Val, XP_047283099.1:p.Asp334Gly, XP_047283099.1:p.Asp334Val

Select item 145536412015.

rs1455364120 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 11:19152568 (GRCh38)
11:19174115 (GRCh37)
Canonical SPDI:: NC_000011.10:19152567:C:G
Gene:: ZDHHC13 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.19152568C>G, NC_000011.9:g.19174115C>G, NM_019028.3:c.757C>G, NM_019028.2:c.757C>G, XM_005252996.3:c.367C>G, XM_005252996.2:c.367C>G, XM_005252996.1:c.367C>G, NM_001001483.3:c.367C>G, NM_001001483.2:c.367C>G, XM_011520194.3:c.817C>G, XM_011520194.2:c.817C>G, XM_011520194.1:c.817C>G, XM_011520195.2:c.367C>G, XM_011520195.1:c.367C>G, XM_047427139.1:c.733C>G, XM_047427138.1:c.817C>G, XM_047427141.1:c.757C>G, XM_047427142.1:c.367C>G, XM_047427140.1:c.817C>G, XM_047427143.1:c.367C>G, XM_047427144.1:c.817C>G, NP_061901.2:p.Pro253Ala, XP_005253053.1:p.Pro123Ala, NP_001001483.1:p.Pro123Ala, XP_011518496.1:p.Pro273Ala, XP_011518497.1:p.Pro123Ala, XP_047283095.1:p.Pro245Ala, XP_047283094.1:p.Pro273Ala, XP_047283097.1:p.Pro253Ala, XP_047283098.1:p.Pro123Ala, XP_047283096.1:p.Pro273Ala, XP_047283099.1:p.Pro123Ala, XP_047283100.1:p.Pro273Ala

Select item 145342608216.

rs1453426082 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:19155926 (GRCh38)
11:19177473 (GRCh37)
Canonical SPDI:: NC_000011.10:19155925:C:T
Gene:: ZDHHC13 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000011.10:g.19155926C>T, NC_000011.9:g.19177473C>T, NM_019028.3:c.1004C>T, NM_019028.2:c.1004C>T, XM_005252996.3:c.614C>T, XM_005252996.2:c.614C>T, XM_005252996.1:c.614C>T, NM_001001483.3:c.614C>T, NM_001001483.2:c.614C>T, XM_011520194.3:c.1064C>T, XM_011520194.2:c.1064C>T, XM_011520194.1:c.1064C>T, XM_011520195.2:c.614C>T, XM_011520195.1:c.614C>T, XM_047427139.1:c.980C>T, XM_047427138.1:c.1064C>T, XM_047427141.1:c.1004C>T, XM_047427142.1:c.614C>T, XM_047427140.1:c.1064C>T, XM_047427143.1:c.614C>T, XM_047427144.1:c.1064C>T, NP_061901.2:p.Pro335Leu, XP_005253053.1:p.Pro205Leu, NP_001001483.1:p.Pro205Leu, XP_011518496.1:p.Pro355Leu, XP_011518497.1:p.Pro205Leu, XP_047283095.1:p.Pro327Leu, XP_047283094.1:p.Pro355Leu, XP_047283097.1:p.Pro335Leu, XP_047283098.1:p.Pro205Leu, XP_047283096.1:p.Pro355Leu, XP_047283099.1:p.Pro205Leu, XP_047283100.1:p.Pro355Leu

Select item 145310842017.

rs1453108420 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:19158954 (GRCh38)
11:19180501 (GRCh37)
Canonical SPDI:: NC_000011.10:19158953:A:G
Gene:: ZDHHC13 (Varview)
Functional Consequence:: intron_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000007/1 (GnomAD_exomes)
G=0.000015/4 (TOPMED)
HGVS:: NC_000011.10:g.19158954A>G, NC_000011.9:g.19180501A>G, NM_019028.3:c.1022A>G, NM_019028.2:c.1022A>G, XM_005252996.3:c.632A>G, XM_005252996.2:c.632A>G, XM_005252996.1:c.632A>G, NM_001001483.3:c.632A>G, NM_001001483.2:c.632A>G, XM_011520194.3:c.1082A>G, XM_011520194.2:c.1082A>G, XM_011520194.1:c.1082A>G, XM_011520195.2:c.632A>G, XM_011520195.1:c.632A>G, XM_047427139.1:c.998A>G, XM_047427138.1:c.1082A>G, XM_047427141.1:c.1022A>G, XM_047427142.1:c.632A>G, XM_047427140.1:c.1082A>G, XM_047427143.1:c.632A>G, NP_061901.2:p.Tyr341Cys, XP_005253053.1:p.Tyr211Cys, NP_001001483.1:p.Tyr211Cys, XP_011518496.1:p.Tyr361Cys, XP_011518497.1:p.Tyr211Cys, XP_047283095.1:p.Tyr333Cys, XP_047283094.1:p.Tyr361Cys, XP_047283097.1:p.Tyr341Cys, XP_047283098.1:p.Tyr211Cys, XP_047283096.1:p.Tyr361Cys, XP_047283099.1:p.Tyr211Cys

Select item 145139932818.

rs1451399328 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:19152238 (GRCh38)
11:19173785 (GRCh37)
Canonical SPDI:: NC_000011.10:19152237:A:G
Gene:: ZDHHC13 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.19152238A>G, NC_000011.9:g.19173785A>G, NM_019028.3:c.665A>G, NM_019028.2:c.665A>G, XM_005252996.3:c.275A>G, XM_005252996.2:c.275A>G, XM_005252996.1:c.275A>G, NM_001001483.3:c.275A>G, NM_001001483.2:c.275A>G, XM_011520194.3:c.725A>G, XM_011520194.2:c.725A>G, XM_011520194.1:c.725A>G, XM_011520195.2:c.275A>G, XM_011520195.1:c.275A>G, XM_047427139.1:c.641A>G, XM_047427138.1:c.725A>G, XM_047427141.1:c.665A>G, XM_047427142.1:c.275A>G, XM_047427140.1:c.725A>G, XM_047427143.1:c.275A>G, XM_047427144.1:c.725A>G, NP_061901.2:p.His222Arg, XP_005253053.1:p.His92Arg, NP_001001483.1:p.His92Arg, XP_011518496.1:p.His242Arg, XP_011518497.1:p.His92Arg, XP_047283095.1:p.His214Arg, XP_047283094.1:p.His242Arg, XP_047283097.1:p.His222Arg, XP_047283098.1:p.His92Arg, XP_047283096.1:p.His242Arg, XP_047283099.1:p.His92Arg, XP_047283100.1:p.His242Arg

Select item 144945723519.

rs1449457235 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:19155808 (GRCh38)
11:19177355 (GRCh37)
Canonical SPDI:: NC_000011.10:19155807:C:T
Gene:: ZDHHC13 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000019/5 (TOPMED)
HGVS:: NC_000011.10:g.19155808C>T, NC_000011.9:g.19177355C>T, NM_019028.3:c.886C>T, NM_019028.2:c.886C>T, XM_005252996.3:c.496C>T, XM_005252996.2:c.496C>T, XM_005252996.1:c.496C>T, NM_001001483.3:c.496C>T, NM_001001483.2:c.496C>T, XM_011520194.3:c.946C>T, XM_011520194.2:c.946C>T, XM_011520194.1:c.946C>T, XM_011520195.2:c.496C>T, XM_011520195.1:c.496C>T, XM_047427139.1:c.862C>T, XM_047427138.1:c.946C>T, XM_047427141.1:c.886C>T, XM_047427142.1:c.496C>T, XM_047427140.1:c.946C>T, XM_047427143.1:c.496C>T, XM_047427144.1:c.946C>T

Select item 144829485420.

rs1448294854 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:19149322 (GRCh38)
11:19170869 (GRCh37)
Canonical SPDI:: NC_000011.10:19149321:A:G
Gene:: ZDHHC13 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.19149322A>G, NC_000011.9:g.19170869A>G, NM_019028.3:c.510A>G, NM_019028.2:c.510A>G, XM_005252996.3:c.120A>G, XM_005252996.2:c.120A>G, XM_005252996.1:c.120A>G, NM_001001483.3:c.120A>G, NM_001001483.2:c.120A>G, XM_011520194.3:c.570A>G, XM_011520194.2:c.570A>G, XM_011520194.1:c.570A>G, XM_011520195.2:c.120A>G, XM_011520195.1:c.120A>G, XM_047427139.1:c.486A>G, XM_047427138.1:c.570A>G, XM_047427141.1:c.510A>G, XM_047427142.1:c.120A>G, XM_047427140.1:c.570A>G, XM_047427143.1:c.120A>G, XM_047427144.1:c.570A>G

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