View genomic variant #0000000042

Chromosome 13
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.32969071G>C
Reference -
DB-ID BRCA2_000013
Frequency -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Florian Bayersdorfer




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BRCA2 NM_000059.3 ./+? 25 c.9501+1G>C r.spl? p.?