Variant #0000190796 (NC_000017.10:g.41256086_41256097del, NC_000017.10(NM_007294.3):c.441+52_441+63del (BRCA1))
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.41256086_41256097del |
DNA change (hg38) |
g.43104069_43104080del |
Published as |
- |
ISCN |
- |
DB-ID |
BRCA1_001952 See all 6 reported entries |
Variant remarks |
Class 1 not pathogenic based on frequency >1% in an outbred sampleset. Frequency 0.3559 (European), 0.3321 (African), 0.4006 (Admixed American/Latino), 0.3899 (East Asian), 0.5204 (South Asian), derived from 1000 genomes (2013-05-02). |
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 |
Creative Commons Attribution 4.0 International |
Created by |
ENIGMA consortium |
Date created |
2016-09-28 12:00:00 +02:00 (CEST) |
Date last edited |
2020-07-13 15:42:55 +02:00 (CEST) |

Variant on transcripts
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