Variant #0000016685 (NC_000011.9:g.3000_3001insA, TMEM151A(NM_153266.4):c.623_624insA)
Chromosome |
11 |
Allele |
Maternal (confirmed) |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Probably affects function |
Type |
Insertion |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.3000_3001insA |
Reference |
GenBank |
DB-ID |
TMEM151A_000623 |
Frequency |
1/36 patients |
Variant remarks |
Identified in one sporadic patient(Cell Discov. 2021;7(1):83.) |
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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