Variant #0001006006 (NC_000022.10:g.30189608_30189618dup, NM_032204.4:c.1739_1749dup (ASCC2))

Chromosome 22
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.30189608_30189618dup
DNA change (hg38) -
Published as ASCC2(NM_032204.4):c.1739_1749dupTGGCGGCACAG (p.(Arg584fs))
ISCN -
DB-ID ASCC2_000002
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ASCC2 NM_032204.4 ?/. - c.1739_1749dup r.(?) p.(Arg584Trpfs*69)


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