Variant #0000000261 (NC_000017.10:g.59821930C>T, NM_032043.2:c.2120G>A (BRIP1))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.59821930C>T
Reference -
DB-ID BRIP1_000005
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 2023-06-27 13:48:58 +00:00 (UTC)
Date last edited 2023-06-27 13:50:16 +00:00 (UTC)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BRIP1 NM_032043.2 ?/? 15 c.2120G>A r.(?) p.(Arg707His)