Variant #0000053238 (NC_000013.10:g.32900433C>T, NC_000013.10(NM_000059.3):c.516+14C>T (BRCA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.32900433C>T
DNA change (hg38) g.32326296C>T
Published as c.516+14C>T
ISCN -
DB-ID BRCA2_000030 See all 30 reported entries
Variant remarks mRNA analysis and splicing reporter minigene; predicted neutral
Reference PubMed: Bonnet 2008
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00034 View details
Owner Peter Devilee
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Maaike Vreeswijk
Date created 2009-10-03 17:15:53 +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 -/. 6i c.516+14C>T r.= ? -


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