Variant #0000000285 (NC_000022.10:g.29121228T>C, NC_000022.10(NM_007194.3):c.444+3A>G (CHEK2))

Chromosome 22
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.29121228T>C
Reference -
DB-ID CHEK2_000015
Frequency -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2023-06-29 12:55:50 +00:00 (UTC)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHEK2 NM_007194.3 ?/? 3 c.444+3A>G r.spl? p.?