Variant #0000053725 (NC_000013.10:g.32937506G>C, NM_000059.3:c.8167G>C (BRCA2))
| Chromosome |
13 |
| 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.32937506G>C |
| DNA change (hg38) |
g.32363369G>C |
| Published as |
D2723H |
| ISCN |
- |
| DB-ID |
BRCA2_000290 See all 63 reported entries |
| Variant remarks |
Multifactorial likelihood-ratio model; predicted deleterious |
| Reference |
PubMed: Goldgar 2004 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Peter Devilee |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Maaike Vreeswijk |
| Date created |
2009-10-03 17:15:54 +02:00 (CEST) |
| Date last edited |
2020-07-03 16:01:33 +02:00 (CEST) |

Variant on transcripts
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