Variant #0000409894 (NC_000013.10:g.32889757T>G, NM_000059.3:c.-87T>G (BRCA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.32889757T>G
DNA change (hg38) g.32315620T>G
Published as -
ISCN -
DB-ID BRCA2_006639 See all 2 reported entries
Variant remarks expression cloning luciferase assay no effect
Reference PubMed: Burke 2018, Journal: Burke 2018
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Lez J Burke
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2018-10-27 18:08:29 +02:00 (CEST)
Date last edited 2019-02-07 08:32:11 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA2 NM_000059.3 ?/. 1 c.-87T>G r.= p.= -


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