Variant #0000054121 (NC_000013.10:g.32889805G>A, NC_000013.10(NM_000059.3):c.-40+1G>A (BRCA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.32889805G>A
DNA change (hg38) g.32315668G>A
Published as c.-40+1G>A
ISCN -
DB-ID BRCA2_000520 See all 3 reported entries
Variant remarks Embryonic stem cell assay, RNA analysis; strong functional effect, disruption exon 1 donor site, use of alternative donor site middle of exon 1 (BRCA2 c.-139)
Reference PubMed: Bakker 2014
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Janine Bakker
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Maaike Vreeswijk
Date created 2014-01-09 10:50:36 +01:00 (CET)
Date last edited 2019-02-25 21:51:16 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA2 NM_000059.3 +?/. 1i c.-40+1G>A r.-138_-40del p.(=) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.