Variant #0000890773 (NC_000012.11:g.7047678G>A, NM_001007026.1:c.2552G>A (ATN1))

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.7047678G>A
DNA change (hg38) -
Published as ATN1(NM_001940.4):c.2552G>A (p.C851Y)
ISCN -
DB-ID C12orf57_000024
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
ATN1 NM_001007026.1 ?/. - c.2552G>A - r.(?) p.(Cys851Tyr)
C12orf57 NM_138425.2 ?/. - c.-5607G>A - r.(?) p.(=)


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