Variant #0000193391 (NC_000013.10:g.32953453G>A, NC_000013.10(NM_000059.3):c.8755-1G>A (BRCA2))

Chromosome 13
Allele Parent #1
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.32953453G>A
DNA change (hg38) g.32379316G>A
Published as -
ISCN -
DB-ID BRCA2_001084 See all 18 reported entries
Variant remarks Insufficient evidence to determine clinical significance. Variant allele produces r.8755_8953del, r.8755_9004del AND full-length transcripts.
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 2016-04-15 12:00:00 +02:00 (CEST)
Date last edited 2020-07-03 16:09:47 +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 ?/? 21i c.8755-1G>A r.spl p.? -


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