Variant #0000193158 (NC_000013.10:g.32937507A>G, NM_000059.3:c.8168A>G (BRCA2))
Chromosome |
13 |
Allele |
Parent #1 |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
Classification method |
- |
Clinical classification |
pathogenic (dominant) |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.32937507A>G |
DNA change (hg38) |
g.32363370A>G |
Published as |
- |
ISCN |
- |
DB-ID |
BRCA2_000292 See all 19 reported entries |
Variant remarks |
IARC class based on posterior probability from multifactorial likelihood analysis, thresholds for class as per Plon 2008 (PMID:18951446). Class 5 based on posterior probability = 1 |
Reference |
ENIGMA classification criteria, Details in BRCA database Tavtigian lab, PubMed: Guidigli 2013 |
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 |
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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