Variant #0000000567 (NC_000013.11:g.32333303C>G, NM_000059.3:c.1825C>G (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.32333303C>G
Published as -
Reference Kah Nyin Lai et al. (2017), dbSNP, ClinVar
DB-ID BRCA2_000070
dbSNP ID rs80358472
Frequency 2/1218
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 11:50:24 +08:00 (CST)
Date last edited 2021-08-23 09:00:34 +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.1825C>G - r.(?) p.(Gln609Glu) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000118 DNA ? BRCA2 25 Nuur Athirah Binti Mohd Daud