Variant #0000040337 (NC_000017.10:g.(41267797_41276033)_(41277500_?)del, BRCA1(NM_007294.3):c.-232_(80+1_81-1){0})
Individual ID |
00019881 |
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.(41267797_41276033)_(41277500_?)del |
DNA change (hg38) |
- |
Published as |
c.-232-?_80+?del |
ISCN |
- |
DB-ID |
BRCA1_001184 See all 29 reported entries |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Unknown |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Rien Blok |
Database submission license |
No license selected |
Created by |
Rien Blok |

Variant on transcripts
Screenings
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