Variant #0000000584 (NC_000013.11:g.32396934C>T, NM_000059.3:c.9538C>T (BRCA2))

Individual ID 00000103
Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.32396934C>T
Published as -
Reference Kah Nyin Lai et al. (2017), dbSNP, ClinVar
DB-ID BRCA2_000080
dbSNP ID rs200598289
Frequency 1/2089
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nuur Athirah Binti Mohd Daud
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nuur Athirah Binti Mohd Daud
Date created 2020-10-28 15:33:39 +08:00 (CST)
Date last edited 2021-08-23 09:36:17 +08:00 (CST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
BRCA2 NM_000059.3 ?/. - c.9538C>T - r.(?) p.(Leu3180Phe) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000118 DNA ? BRCA2 25 Nuur Athirah Binti Mohd Daud