Variant #0000016695 (NC_000011.9:g.2506G>A, TMEM151A(NM_153266.4):c.129G>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.2506G>A |
Reference |
- |
DB-ID |
TMEM151A_001276 |
Frequency |
1/521 patients |
Variant remarks |
identified in one sporadic PKD patient(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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