Variant #0000054146 (NC_000013.10:g.32893237T>C, NM_000059.3:c.91T>C (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.32893237T>C
DNA change (hg38) g.32319100T>C
Published as -
ISCN -
DB-ID BRCA2_000546 See all 4 reported entries
Variant remarks Embryonic stem cell assay; no rescue ES cell lethality
Reference PubMed: Biswas 2012
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 2014-02-19 21:46:42 +01:00 (CET)
Date last edited 2020-07-03 14:50:02 +02:00 (CEST)
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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.91T>C r.(?) p.Try31Arg -


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