Variant #0000000005 (NC_000016.9:g.23635348A>C, NM_024675.3:c.2816T>G (PALB2))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.23635348A>C
Reference -
DB-ID PALB2_000001
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00096 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2017-05-15 09:00:24 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PALB2 NM_024675.3 ?/? 8 c.2816T>G r.(?) p.(Leu939Trp)