Variant #0000192480 (NC_000013.10:g.32914451C>T, NM_000059.3:c.5959C>T (BRCA2))
| Chromosome |
13 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
pathogenic (dominant) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.32914451C>T |
| DNA change (hg38) |
g.32340314C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
BRCA2_004858 See all 7 reported entries |
| Variant remarks |
Variant allele predicted to encode truncated non-functional protein |
| Reference |
ENIGMA classification criteria |
| 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 |
2016-09-08 12:00:00 +02:00 (CEST) |
| Date last edited |
2020-02-20 16:18:07 +01:00 (CET) |

Variant on transcripts
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