Variant #0000016688 (NC_000011.9:g.3759A>C, TMEM151A(NM_153266.4):c.1382A>C)
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Probably does not affect function |
Type |
Substitution |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.3759A>C |
Reference |
GenBank |
DB-ID |
TMEM151A_001273 |
Frequency |
- |
Variant remarks |
one PKD patient was detected to have compound heterozygous variants in TMEM151A (c.469C>T and c.1382A>C). And the variant c.1382A>C was inherited from his asymptomatic father ,while the variant c.469C>T was inherited from his mother, who also had PKD.(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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