Variant #0000695063 (NC_000016.9:g.23646645A>G, NM_024675.3:c.1222T>C (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.23646645A>G
DNA change (hg38) g.23635324A>G
Published as -
ISCN -
DB-ID PALB2_010067 See all 3 reported entries
Variant remarks expression cloning HR efficiency 92,32%, PARPi resistance 108,51%, cisplatin resistance 93,33%, normalised cells 79,77%
Reference PubMed: Boonen 2019
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
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 14:57:26 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
PALB2 NM_024675.3 -?/. - c.1222T>C - p.(Tyr408His) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.