Variant #0000695112 (NC_000016.9:g.23625398C>G, PALB2(NM_024675.3):c.3128G>C)
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.23625398C>G |
DNA change (hg38) |
g.23614077C>G |
Published as |
- |
ISCN |
- |
DB-ID |
PALB2_010151 See all 6 reported entries |
Variant remarks |
expression cloning relative homology directed repair 4.9 |
Reference |
PubMed: Wiltshire 2020 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
0 |
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 |

Variant on transcripts
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