Variant #0000053222 (NC_000013.10:g.32893291G>T, NM_000059.3:c.145G>T (BRCA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.32893291G>T
DNA change (hg38) g.32319154G>T
Published as -
ISCN -
DB-ID BRCA2_000017 See all 28 reported entries
Variant remarks ESEfinder/ESRsearch, hybrid minigenes; ESE disruption, skipping of exon 3 is almost total, but a small fraction of mRNA species with r.145g>u change is present
Reference PubMed: Sanz 2010
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Eladio A Velasco
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Maaike Vreeswijk
Date created 2010-07-02 09:57:25 +02:00 (CEST)
Date last edited 2019-02-25 21:51:16 +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 +/. 3 c.145G>T r.68_316del p.[Asp23_Leu105del, Glu49*] -


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