Variant #0000080013 (NC_000016.9:g.23619238_23619242del, PALB2(NM_024675.3):c.3294_3298del)

Individual ID 00051022
Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.23619238_23619242del
DNA change (hg38) g.23607917_23607921del
Published as -
ISCN -
DB-ID PALB2_000006 See all 4 reported entries
Variant remarks -
Reference PubMed: Reid 2007
ClinVar ID -
dbSNP ID rs180177134
Origin Germline
Segregation -
Frequency -
Re-site HinfI-, MlyI-, PleI-
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Marc Tischkowitz
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Marc Tischkowitz
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
PALB2 NM_024675.3 +/+ 12 c.3294_3298del r.(?) p.(Lys1098Asnfs*23) -



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000050967 DNA ? - - PALB2 1 Marc Tischkowitz