Variant #0000000622 (NC_000013.11:g.32376739G>A, NM_000059.3:c.8702G>A (BRCA2))

Individual ID 00000109
Chromosome 13
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.32376739G>A
Published as -
Reference P S Ng et al. (2016), dbSNP, ClinVar
DB-ID BRCA2_000034 See all 5 reported entries
dbSNP ID rs80359129
Frequency 1/8
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 2020-11-01 16:07:10 +08:00 (CST)
Date last edited 2021-08-22 11:24:02 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
BRCA2 NM_000059.3 ./. 21 c.8702G>A - r.(?) p.(Gly2901Asp) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000124 DNA SEQ BRCA2 8 Nuur Athirah Binti Mohd Daud