Variant #0000002207 (NC_000013.11:g.32337924G>T, NM_000059.3:c.3569G>T (BRCA2))

Individual ID 00000426
Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.32337924G>T
Published as -
Reference Wei Xiong Wen et al. (2018), dbSNP, ClinVar
DB-ID BRCA2_000161
dbSNP ID rs80358605
Frequency 1/490
Variant remarks VUS (variants of unknown significance)
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 2021-02-25 15:35:20 +08:00 (CST)
Date last edited 2021-08-01 12:53:47 +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.3569G>T - r.(?) p.(Arg1190Leu) missense Uncertain significance​



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000455 DNA MLPA;SEQ-NG-I BRCA2 13 Nuur Athirah Binti Mohd Daud