Variant #0000053249 (NC_000013.10:g.32900752T>G, NC_000013.10(NM_000059.3):c.631+2T>G (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.32900752T>G
DNA change (hg38) g.32326615T>G
Published as IVS7+2T>G
ISCN -
DB-ID BRCA2_000039 See all 19 reported entries
Variant remarks Mouse ES cell assay, RNA analysis; no rescue ES cell lethality; upregulation alternative spliced transcript delta 4-7
Reference PubMed: Biswas 2011
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Maaike Vreeswijk
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Maaike Vreeswijk
Date created 2012-06-21 11:44:11 +02:00 (CEST)
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 +?/. 7i c.631+2T>G r.spl not applicable -


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