Variant #0000016677 (NC_000011.9:g.3116G>T, TMEM151A(NM_153266.4):c.739G>T)

Chromosome 11
Allele Parent #1
Affects function (as reported) Effect unknown
Affects function (by curator) Probably affects function
Type Substitution
DNA change (genomic) (Relative to hg19 / GRCh37) g.3116G>T
Reference GenBank
DB-ID TMEM151A_000898
Frequency -
Variant remarks also identified in asymptomatic parents, possible incomplete penetrance.(Cell Discov. 2021;7(1):83;Mov Disord. 2022;37(3):608-613)
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM151A NM_153266.4 ?/+? 2 c.739G>T r.739g>u p.E247*