Variant #0000054119 (NC_000013.10:g.32900700G>A, NM_000059.3:c.581G>A (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.32900700G>A |
| DNA change (hg38) |
g.32326563G>A |
| Published as |
809G>A |
| ISCN |
- |
| DB-ID |
BRCA2_000517 See all 13 reported entries |
| Variant remarks |
Mouse ES cell assay, RNA analysis, partial exon 7 deletion ; partial rescue lethality; HR as wt |
| Reference |
PubMed: Biswas 2011 |
| 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 |
2012-06-21 11:40:05 +02:00 (CEST) |
| Date last edited |
2019-02-25 21:51:16 +01:00 (CET) |

Variant on transcripts
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