Variant #0000189407 (NC_000017.10:g.41231335G>A, NC_000017.10(NM_007294.3):c.4358-2704C>T (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.41231335G>A |
DNA change (hg38) |
g.43079318G>A |
Published as |
- |
ISCN |
- |
DB-ID |
BRCA1_002731 See all 6 reported entries |
Variant remarks |
Class 1 not pathogenic based on frequency >1% in an outbred sampleset. Frequency 0.0115 (Admixed American/Latino), 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) |
4.0E-5 View details |
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 |
2017-08-18 17:34:35 +02:00 (CEST) |

Variant on transcripts
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