Variant #0000002606 (NC_000006.12:g.7231C>T, CYP21A2(NM_000500.9):c.1069C>T)

Individual ID 00000582
Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.7231C>T
Published as p.R356W
Reference P Balraj et al.(2013)
DB-ID CYP21A2_000001
dbSNP ID rs7769409
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nur Aisyah Athirah
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nur Aisyah Athirah
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

Clinical classification     
CYP21A2 NM_000500.9 +/. 8 c.1069C>T - r.(?) p.(Arg357Trp) Pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000643 DNA MLPA;PCRdig;SEQ;Southern CYP21A2 5 Nur Aisyah Athirah