Variant #0000054379 (NC_000017.10:g.41249263G>A, NM_007294.3:c.591C>T (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.41249263G>A |
| DNA change (hg38) |
g.43097246G>A |
| Published as |
c.591C>T |
| ISCN |
- |
| DB-ID |
BRCA1_000096 See all 34 reported entries |
| Variant remarks |
splicing reporter minigene; 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) |
0.00154 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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