Variant #0000011747 (NC_000013.11:g.32398161G>T, BRCA2(NM_000059.3):c.9649-1G>T)

Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg38 / GRCh38) g.32398161G>T
Reference -
DB-ID BRCA2_000324 See all 2 reported entries
dbSNP ID rs1555289898
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Pablo Kalfayan-Hospital Italiano
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Instituto Nacional del Cancer
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Zygosity     

Co_ocurrence     

Review status     
BRCA2 NM_000059.3 ?/? 26i c.9649-1G>T r.spl? p.(?) Hetero no -