Variant #0000053235 (NC_000013.10:g.32900191G>T, NC_000013.10(NM_000059.3):c.426-47G>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.32900191G>T
DNA change (hg38) g.32326054G>T
Published as IVS4-47G/T
ISCN -
DB-ID BRCA2_000026 See all 2 reported entries
Variant remarks Prevalence in normal controls; predicted neutral
Reference PubMed: Wagner 1999
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 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 2020-07-03 14:53:18 +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 -/. 4i c.426-47G>T r.(=) ? -


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