Variant #0000021773 (NC_000017.10:g.41203103C>A, NM_007294.3:c.5309G>T (BRCA1))
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.41203103C>A |
DNA change (hg38) |
g.43051086C>A |
Published as |
- |
ISCN |
- |
DB-ID |
BRCA1_001008 See all 60 reported entries |
Variant remarks |
Classified by NLB-labs |
Reference |
R. vd Luijt |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
yes |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Rob B. van der Luijt |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2013-11-09 17:39:12 +01:00 (CET) |
Date last edited |
2016-08-05 14:13:49 +02:00 (CEST) |

Variant on transcripts
|