Variant #0000000366 (NC_000016.9:g.23635391C>G, NM_024675.3:c.2773G>C (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.23635391C>G
Reference -
DB-ID PALB2_000007
Frequency -
Average frequency (gnomAD v.2.1.1) 2.0E-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 2023-07-18 08:45:10 +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     
PALB2 NM_024675.3 ?/? 8 c.2773G>C r.(?) p.(Val925Leu)