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 InternationalCreative Commons License
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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA2 NM_000059.3 +/+ 18 c.8168A>G r.(?) p.(Asp2723Gly) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.