Variant #0000002156 (NC_000017.11:g.43091807T>C, NM_007294.3:c.3724A>G (BRCA1))

Individual ID 00000408
Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.43091807T>C
Published as -
Reference Wei Xiong Wen et al. (2018), dbSNP, ClinVar
DB-ID BRCA1_000102
dbSNP ID rs80357037
Frequency 1/490
Variant remarks VUS (variants of unknown significance)
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 2021-02-24 12:15:25 +08:00 (CST)
Date last edited 2021-08-01 11:21:49 +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     
BRCA1 NM_007294.3 +/. - c.3724A>G - r.(?) p.(Thr1242Ala) missense Benign



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000423 DNA MLPA;SEQ-NG-I BRCA1 20 Nuur Athirah Binti Mohd Daud