Variant #0000189904 (NC_000017.10:g.41244429C>T, NM_007294.3:c.3119G>A (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.41244429C>T |
DNA change (hg38) |
g.43092412C>T |
Published as |
- |
ISCN |
- |
DB-ID |
BRCA1_000233 See all 169 reported entries |
Variant remarks |
IARC class based on posterior probability from multifactorial likelihood analysis, thresholds for class as per Plon 2008 (PMID:18951446). Class 1 based on posterior probability = 0.00000000000204. Also class 1 based on frequency >1% in an outbred sampleset. Frequency 0.02111 (European), derived from 1000 genomes (2012-04-30). |
Reference |
ENIGMA classification criteria, Details in BRCA database Tavtigian lab, PubMed: Lindor 2012 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.01318 View details |
Owner |
ENIGMA consortium |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
ENIGMA consortium |
Date created |
2015-10-08 12:00:00 +02:00 (CEST) |
Date last edited |
2020-03-29 13:34:55 +02:00 (CEST) |

Variant on transcripts
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