Variant #0000001157 (NC_000009.12:g.132928808C>T, TSC1(NM_000368.4):c.65G>A)

Individual ID 00000234
Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.132928808C>T
Published as R22Q
Reference Nur Farrah Dila Ismail et al. (2017), dbSNP, ClinVar
DB-ID TSC1_000001
dbSNP ID rs141736779
Frequency 1/4
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
TSC1 NM_000368.4 +/. 3 c.65G>A - r.(?) p.(Arg22Gln) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000249 DNA MLPA;PCRlr;SEQ TSC1 3 Nuur Athirah Binti Mohd Daud