Variant #0000000532 (NC_000017.11:g.43115746C>T, NM_007294.3:c.114G>A (BRCA1))

Individual ID 00000095
Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.43115746C>T
Published as -
Reference Gaik Theng Toh et al. (2008), dbSNP, ClinVar
DB-ID BRCA1_000038 See all 3 reported entries
dbSNP ID rs1800062
Frequency 1/37
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 11:49:29 +08:00 (CST)
Date last edited 2021-08-22 16:11:14 +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 -/. 3 c.114G>A - r.(=) p.(=) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000110 DNA PCR BRCA1 13 Nuur Athirah Binti Mohd Daud