Variant #0000016698 (NC_000011.9:g.2874C>A, TMEM151A(NM_153266.4):c.497C>A)

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type Substitution
DNA change (genomic) (Relative to hg19 / GRCh37) g.2874C>A
Reference -
DB-ID TMEM151A_001279
Frequency 1/521 patients
Variant remarks identified in one sporadic PKD patient(Mov Disord. 2022;37(3):545-552)
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Yulan Chen
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Yulan Chen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM151A NM_153266.4 ?/? 2 c.497C>A r.497c>a p.T166K