Variant #0000192865 (NC_000013.10:g.32928996A>T, NC_000013.10(NM_000059.3):c.7008-2A>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.32928996A>T
DNA change (hg38) g.32354859A>T
Published as -
ISCN -
DB-ID BRCA2_000177 See all 15 reported entries
Variant remarks Allele-specific assay on patient-derived mRNA demonstrated that the variant allele produces only predicted non-functional transcripts. Variant allele produces r.7008_7435del, r.7008_7017del, and r.7008_7253del transcripts (encoding predicted non-functional proteins).
Reference ENIGMA classification criteria, PubMed: Colombo 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 2016-04-03 12:00:00 +02:00 (CEST)
Date last edited 2020-07-03 15:48:18 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA2 NM_000059.3 +/+ 13i c.7008-2A>T r.[7008_7435del, 7008_7017del, 7008_7253del] p.? -


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