Variant #0000000140 (NC_000022.10:g.29091154T>C, NM_007194.3:c.1336A>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.29091154T>C
Reference -
DB-ID CHEK2_000009
Frequency -
Average frequency (gnomAD v.2.1.1) 7.0E-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 2023-06-16 11:04:04 +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 ?/? 12 c.1336A>G r.(?) p.(Asn446Asp)