Variant #0000000642 (NC_000013.11:g.32346841C>T, BRCA2(NM_000059.3):c.6952C>T)

Individual ID 00000116
Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.32346841C>T
Published as -
Reference Hanis Nazihah Hasmad et al. (2016), dbSNP, ClinVar
DB-ID BRCA2_000091 See all 2 reported entries
dbSNP ID rs80358920
Frequency 1/2
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
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 +/. 13 c.6952C>T - r.(?) p.(Arg2318*) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000131 DNA PCRm;SEQ BRCA2 2 Nuur Athirah Binti Mohd Daud