Variant #0000000082 (NC_000016.9:g.23647357_23647358del, NM_024675.3:c.509_510del (PALB2))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.23647357_23647358del
Reference -
DB-ID PALB2_000003
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 2020-03-03 12:43:08 +00:00 (UTC)
Date last edited 2025-10-09 11:51:18 +00:00 (UTC)
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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.509_510del r.(?) p.(Arg170Ilefs*14) pathogenic