Variant #0000192534 (NC_000013.10:g.32914592C>T, NM_000059.3:c.6100C>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.32914592C>T
DNA change (hg38) g.32340455C>T
Published as -
ISCN -
DB-ID BRCA2_000152 See all 81 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 = 0.00000571
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) 0.00309 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 -/- 11 c.6100C>T r.(?) p.(Arg2034Cys) -


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