Variant #0000695024 (NC_000016.9:g.23614792G>C, NM_024675.3:c.3549C>G (PALB2))
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.23614792G>C |
DNA change (hg38) |
g.23603471G>C |
Published as |
- |
ISCN |
- |
DB-ID |
PALB2_000008 See all 17 reported entries |
Variant remarks |
expression cloning HR efficiency 11,12%, PARPi resistance 9,67%, cisplatin resistance 19,53%, normalised cells 344,61% |
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) |
2.0E-5 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
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