Variant #0000192995 (NC_000013.10:g.32930747G>A, NC_000013.10(NM_000059.3):c.7617+1G>A (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.32930747G>A
DNA change (hg38) g.32356610G>A
Published as -
ISCN -
DB-ID BRCA2_002239 See all 13 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.7436_7617del transcript (encoding predicted non-functional protein).
Reference ENIGMA classification criteria, PubMed: de Garibay 2014
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 2016-04-15 12:00:00 +02:00 (CEST)
Date last edited 2020-07-03 15:53:55 +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 +/+ 15i c.7617+1G>A r.5278_5332del p.? -


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