Variant #0000055775 (NC_000017.10:g.41267809G>T, NC_000017.10(NM_007294.3):c.81-13C>A (BRCA1))
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.41267809G>T |
| DNA change (hg38) |
g.43115792G>T |
| Published as |
c.81-13C>A |
| ISCN |
- |
| DB-ID |
BRCA1_000540 |
| Variant remarks |
splicing reporter minigene/patient RNA analysis; no splicing defect |
| Reference |
PubMed: Théry 2011 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
7.0E-5 View details |
| Owner |
Maaike Vreeswijk |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Maaike Vreeswijk |
| Date created |
2014-02-19 14:08:12 +01:00 (CET) |
| Date last edited |
2019-02-25 21:12:28 +01:00 (CET) |

Variant on transcripts
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