Variant #0000000644 (NC_000013.11:g.32332434_32332435insA, NM_000059.3:c.956_957insA (BRCA2))

Individual ID 00000117
Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.32332434_32332435insA
Published as -
Reference Hanis Nazihah Hasmad et al. (2016)
DB-ID BRCA2_000093
dbSNP ID -
Frequency 1/3
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 2020-11-02 14:41:30 +08:00 (CST)
Date last edited 2020-12-03 09:25:06 +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 +/. 10 c.956_957insA - r.(?) p.(Asn319Lysfs*8) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000132 DNA PCRm;SEQ BRCA2 3 Nuur Athirah Binti Mohd Daud