Variant #0000000657 (NC_000013.11:g.173208G>A, NM_000059.3:c.-32142499G>A (BRCA2))

Individual ID 00000123
Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.173208G>A
Published as -
Reference Rahimah Ahmad et al. (2013), dbSNP, (OMIM 0174)
DB-ID BRCA2_000096
dbSNP ID rs281864846
Frequency 3/26
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 2020-11-03 14:23:35 +08:00 (CST)
Date last edited 2021-08-19 16:26:26 +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 ?/. 2 c.-32142499G>A - r.(=) p.(=) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000138 ? ? HBA2 1 Nuur Athirah Binti Mohd Daud