Variant #0000622967 (NC_000012.11:g.7053637A>G, NM_001007026.1:c.*2694A>G (ATN1))

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.7053637A>G
DNA change (hg38) g.6944474A>G
Published as C12orf57(NM_001301838.2):c.-55A>G
ISCN -
DB-ID C12orf57_000013
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
ATN1 NM_001007026.1 +/. - c.*2694A>G - r.(=) p.(=)
PTPN6 NM_002831.5 +/. - c.-7039A>G - r.(?) p.(=)
C12orf57 NM_138425.2 +/. - c.53-2A>G - r.spl? p.?


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