Variant #0000054146 (NC_000013.10:g.32893237T>C, NM_000059.3:c.91T>C (BRCA2))
Chromosome |
13 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.32893237T>C |
DNA change (hg38) |
g.32319100T>C |
Published as |
- |
ISCN |
- |
DB-ID |
BRCA2_000546 See all 4 reported entries |
Variant remarks |
Embryonic stem cell assay; no rescue ES cell lethality |
Reference |
PubMed: Biswas 2012 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Maaike Vreeswijk |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
Maaike Vreeswijk |
Date created |
2014-02-19 21:46:42 +01:00 (CET) |
Date last edited |
2020-07-03 14:50:02 +02:00 (CEST) |

Variant on transcripts
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