Variant #0000055643 (NC_000017.10:g.41199693G>C, NM_007294.3:c.5434C>G (BRCA1))
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.41199693G>C |
| DNA change (hg38) |
g.43047676G>C |
| Published as |
c.5434C>G |
| ISCN |
- |
| DB-ID |
BRCA1_000478 See all 12 reported entries |
| Variant remarks |
splicing reporter minigene/patient RNA analysis; major exon skipping |
| Reference |
PubMed: Gaildrat 2010 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0 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
|