Gene DYNC2I1 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: DYNC2I1
Disorder: Short-rib thoracic dysplasia 8 with or without polydactyly
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 DYNC2I1 gene based on the Emirati cohort dataset.
| id |
Chromosome Position |
Gene Name |
HGVS c. (Clinically Relevant) |
HGVS p. (Clinically Relevant) |
Allele Count |
Allele Frequency |
| 742 |
158679717 |
DYNC2I1 |
NM_018051.5:c.941delC |
NP_060521.4:p.Ala314Valfs*4 |
1 |
0.000419% |
| 743 |
158694436 |
DYNC2I1 |
NM_018051.5:c.1066G>T |
NP_060521.4:p.Glu356Ter |
1 |
0.000419% |
