Variant #0000000548 (NC_000017.11:g.43097266C>T, NM_007294.3:c.571G>A (BRCA1))

Individual ID 00000097
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.43097266C>T
Published as -
Reference Kah Nyin Lai et al. (2017), dbSNP, ClinVar
DB-ID BRCA1_000021 See all 2 reported entries
dbSNP ID rs80357090
Frequency 11/1464
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 2020-10-28 09:51:18 +08:00 (CST)
Date last edited 2021-08-22 16:30:53 +08:00 (CST)
Options




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.571G>A - r.(?) p.(Val191Ile) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000112 DNA ? BRCA1 7 Nuur Athirah Binti Mohd Daud