Variant #0000193391 (NC_000013.10:g.32953453G>A, NC_000013.10(NM_000059.3):c.8755-1G>A (BRCA2))
| Chromosome |
13 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.32953453G>A |
| DNA change (hg38) |
g.32379316G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
BRCA2_001084 See all 18 reported entries |
| Variant remarks |
Insufficient evidence to determine clinical significance. Variant allele produces r.8755_8953del, r.8755_9004del AND full-length transcripts. |
| Reference |
ENIGMA classification criteria, PubMed: Colombo 2013 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
ENIGMA consortium |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
ENIGMA consortium |
| Date created |
2016-04-15 12:00:00 +02:00 (CEST) |
| Date last edited |
2020-07-03 16:09:47 +02:00 (CEST) |

Variant on transcripts
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