Variant #0000000518 (NC_000017.11:g.43071077T>C, NM_007294.3:c.4837A>G (BRCA1))

Individual ID 00000093
Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.43071077T>C
Published as -
Reference P Balraj et al. (2002), dbSNP, ClinVar
DB-ID BRCA1_000005 See all 8 reported entries
dbSNP ID rs1799966
Frequency 20/30
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 2020-10-27 10:08:23 +08:00 (CST)
Date last edited 2021-08-22 14:34:57 +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.4837A>G - r.(?) p.(Ser1613Gly) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000108 DNA PCR BRCA1 8 Nuur Athirah Binti Mohd Daud