Variant #0000695122 (NC_000016.9:g.23635348A>C, NM_024675.3:c.2816T>G (PALB2))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.23635348A>C
DNA change (hg38) g.23624027A>C
Published as -
ISCN -
DB-ID PALB2_010126 See all 25 reported entries
Variant remarks expression cloning relative homology directed repair 4.8
Reference PubMed: Wiltshire 2020
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00096 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2020-09-30 15:22:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
PALB2 NM_024675.3 -?/. - c.2816T>G - p.(Leu939Trp) -


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