Variant #0000874025 (NC_000013.10:g.32893225A>G, NM_000059.3:c.79A>G (BRCA2))
| Chromosome |
13 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.32893225A>G |
| DNA change (hg38) |
- |
| Published as |
c.79A>G |
| ISCN |
- |
| DB-ID |
BRCA2_000014 See all 8 reported entries |
| Variant remarks |
classification based on multiple evidence types incl. bioinformatics, RNA analysis, mini-gene splicing assays, clinical data, etc. |
| Reference |
PubMed: Thomassen 2022 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
| Owner |
Maaike Vreeswijk |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Maaike Vreeswijk |
| Date created |
2022-08-04 10:38:26 +02:00 (CEST) |
| Date last edited |
2022-11-15 18:03:57 +01:00 (CET) |

Variant on transcripts
|