Variant #0000192963 (NC_000013.10:g.32930609C>T, NM_000059.3:c.7480C>T (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.32930609C>T
DNA change (hg38) g.32356472C>T
Published as -
ISCN -
DB-ID BRCA2_001038 See all 37 reported entries
Variant remarks Variant allele predicted to encode truncated non-functional protein
Reference ENIGMA classification criteria
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner ENIGMA consortium
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by ENIGMA consortium
Date created 2016-04-22 12:00:00 +02:00 (CEST)
Date last edited 2025-06-08 22:48:30 +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 +/+ 15 c.7480C>T r.(?) p.(Arg2494*) -


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