Gene TMEM138 Details
It offers a comprehensive overview of all clinically relevant variants linked to a specified gene. It provides detailed metrics for each variant, including chromosomal position, HGVS c. and p. notation, allele frequencies, carrier rates, and estimated metrics for at-risk couples. By combining gene-level statistics with specific variant-level data, this page enables an in-depth analysis of how particular genes contribute to disease, thus supporting both clinical interpretation and research efforts.
Gene: TMEM138
Disorder: Joubert syndrome 16
Allele Frequency: 0.00167504
Carrier Rate: 0.00334447
Max At-Risk Couples rate: 0.0000112
The table below lists all clinically relevant variants identified in the TMEM138 gene based on the Emirati cohort dataset.
| id |
Chromosome Position |
Gene Name |
HGVS c. (Clinically Relevant) |
HGVS p. (Clinically Relevant) |
Allele Count |
Allele Frequency |
| 107 |
61136072 |
TMEM138 |
NM_016464.5:c.380C>T |
p.Ala127Val |
3 |
0.001256% |
| 397 |
61131995 |
TMEM138 |
NM_016464.5:c.128+5G>A |
p.? |
1 |
0.000419% |
