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 International |
Created by |
Yulan Chen |

Variant on transcripts
|
|