Variant #0001045493 (NC_000013.10:g.32893207T>A, NC_000013.10(NM_000059.3):c.68-7T>A (BRCA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.32893207T>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID BRCA2_000013 See all 49 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs81002830
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0029 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-06-26 12:50:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA2 NM_000059.3 -/. - c.68-7T>A r.(?) p.(?) -


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