Variant #0000016682 (NC_000011.9:g.2517T>C, TMEM151A(NM_153266.4):c.140T>C)
Chromosome |
11 |
Allele |
Parent #1 |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
Type |
Substitution |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2517T>C |
Reference |
GenBank |
DB-ID |
TMEM151A_000140 |
Frequency |
2/167 patients |
Variant remarks |
identified in sporadic patients (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
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