Variant #0000054128 (NC_000013.10:g.32900744C>T, NM_000059.3:c.625C>T (BRCA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.32900744C>T
DNA change (hg38) g.32326607C>T
Published as c.625C>T
ISCN -
DB-ID BRCA2_000528
Variant remarks splicing reporter minigene; no splicing defect
Reference PubMed: Gaildrat 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 14:34:22 +01:00 (CET)
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 ?/. 7 c.625C>T r.= p.Leu209Phe -


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