Variant #0000055776 (NC_000017.10:g.41267810G>A, BRCA1(NM_007294.3):c.81-14C>T)
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.41267810G>A |
DNA change (hg38) |
g.43115793G>A |
Published as |
c.81-14 C>T |
ISCN |
- |
DB-ID |
BRCA1_000021 See all 25 reported entries |
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) |
0.00039 View details |
Owner |
Maaike Vreeswijk |
Database submission license |
No license selected |
Created by |
Maaike Vreeswijk |

Variant on transcripts
|
|