Variant #0000000041 (NC_000017.10:g.59937223G>C, NM_032043.2:c.139C>G (BRIP1))

Chromosome 17
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.59937223G>C
Reference -
DB-ID BRIP1_000001
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00025 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2018-12-07 11:18:40 +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     
BRIP1 NM_032043.2 ./+? 3 c.139C>G r.(?) p.(Pro47Ala)