Gene SPATA7 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: SPATA7
Disorder: Leber congenital amaurosis 3
Allele Frequency: 0.000837521
Carrier Rate: 0.00167364
Max At-Risk Couples rate: 0.0000028
The table below lists all clinically relevant variants identified in the SPATA7 gene based on the Emirati cohort dataset.
| id |
Chromosome Position |
Gene Name |
HGVS c. (Clinically Relevant) |
HGVS p. (Clinically Relevant) |
Allele Count |
Allele Frequency |
| 448 |
88903909 |
SPATA7 |
NM_018418.5:c.1183C>T |
NP_060888.2:p.Arg395Ter |
1 |
0.000419% |
| 449 |
88904350 |
SPATA7 |
NM_018418.5:c.1384C>T |
NP_060888.2:p.Gln462Ter |
1 |
0.000419% |
