Variant #0000016686 (NC_000011.9:g.3024C>A, TMEM151A(NM_153266.4):c.647C>A)
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Probably affects function |
Type |
Substitution |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.3024C>A |
Reference |
GenBank |
DB-ID |
TMEM151A_000647 |
Frequency |
1/131 patients |
Variant remarks |
identified in one sporadic patient and the variant was drived from de novo (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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