Variant #0000191012 (NC_000017.10:g.41273422C>T, BRCA1(NM_007294.3):c.80+2612G>A)
Chromosome |
17 |
Allele |
Parent #1 |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Does not affect function |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.41273422C>T |
DNA change (hg38) |
g.43121405C>T |
Published as |
- |
ISCN |
- |
DB-ID |
BRCA1_004550 |
Variant remarks |
Class 1 not pathogenic based on frequency >1% in an outbred sampleset. Frequency 0.01187 (European), derived from 1000 genomes (2012-04-30). |
Reference |
ENIGMA classification criteria |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
ENIGMA consortium |
Database submission license |
No license selected |
Created by |
ENIGMA consortium |

Variant on transcripts
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