Variant #0000193163 (NC_000013.10:g.32937526G>T, NM_000059.3:c.8187G>T (BRCA2))

Chromosome 13
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.32937526G>T
DNA change (hg38) g.32363389G>T
Published as -
ISCN -
DB-ID BRCA2_000297 See all 35 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 = 0.0000165. Also class 1 based on frequency >1% in an outbred sampleset. Frequency 0.01224 (Asian), derived from 1000 genomes (2012-04-30).
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) 0.00076 View details
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA2 NM_000059.3 -/- 18 c.8187G>T r.(?) p.(Lys2729Asn) -


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