Variant #0000016684 (NC_000011.9:g.2752C>A, TMEM151A(NM_153266.4):c.375C>A)
| Chromosome |
11 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Probably affects function |
| Type |
Substitution |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2752C>A |
| Reference |
GenBank |
| DB-ID |
TMEM151A_001272 |
| Frequency |
- |
| Variant remarks |
reported by different research groups (Cell Discov. 2021;7(1):83.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 International |
| Created by |
Yulan Chen |

Variant on transcripts
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