Variant #0000691425 (NC_000012.11:g.7047199_7047216dup, NM_001007026.1:c.2486_2503dup (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.7047199_7047216dup
DNA change (hg38) -
Published as ATN1(NM_001940.4):c.2486_2503dupGCGAGAAGGAGCGCGAGC (p.R829_E834dup)
ISCN -
DB-ID C12orf57_000014
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
ATN1 NM_001007026.1 ?/. - c.2486_2503dup - r.(?) p.(Arg829_Glu834dup)
C12orf57 NM_138425.2 ?/. - c.-6086_-6069dup - r.(?) p.(=)


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