Variant #0000053486 (NC_000013.10:g.32914815G>A, NM_000059.3:c.6323G>A (BRCA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.32914815G>A
DNA change (hg38) g.32340678G>A
Published as R2108H
ISCN -
DB-ID BRCA2_000159 See all 28 reported entries
Variant remarks Embryonic stem cell assay; as wildtype control
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) 0.00113 View details
Owner Maaike Vreeswijk
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Maaike Vreeswijk
Date created 2014-02-05 21:32:02 +01:00 (CET)
Date last edited 2020-07-03 15:40:19 +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 -?/. 11 c.6323G>A r.(?) p.Arg2108His -


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