Variant #0000000682 (NC_000016.9:g.23646182C>A, NC_000016.9(NM_024675.3):c.1684+1G>T (PALB2))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.23646182C>A
Reference -
DB-ID PALB2_000008
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2025-10-06 07:51:42 +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     

Class     
PALB2 NM_024675.3 +?/+? 4 c.1684+1G>T r.spl? p.? likely pathogenic