Variant #0000002675 (NC_000001.11:g.19166670A>T, TAS1R2(NM_152232.4):c.1943T>A)

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg38 / GRCh38) g.19166670A>T
Published as -
Reference Chung-Kin Chan et al.(2020)dbSNP
DB-ID TAS1R2_000001
dbSNP ID rs763100088
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 MyHVP
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

Clinical classification     
TAS1R2 NM_152232.4 ?/? - c.1943T>A - r.(?) p.(Ile648Asn) ClinVar