Variant #0000695069 (NC_000016.9:g.23649446T>C, NM_024675.3:c.53A>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.23649446T>C |
DNA change (hg38) |
g.23638125T>C |
Published as |
- |
ISCN |
- |
DB-ID |
PALB2_010016 See all 13 reported entries |
Variant remarks |
expression cloning HR efficiency 100,19%, PARPi resistance 94,47%, cisplatin resistance 84,05%, normalised cells 86,76% |
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) |
0.00138 View details |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2020-09-30 14:57:26 +02:00 (CEST) |
Date last edited |
N/A |

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