Q89* (p.Gln89Ter) variant of NLGN4X (Neuroligin-4, X-linked)
Q89* (p.Gln89Ter) in NLGN4X (Neuroligin-4, X-linked) is a protein-truncating change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.69 / 1. The record also includes population frequency data and structural context.
Q89* (p.Gln89Ter) variant details
- p.Gln89Ter
- ExAC rs745466136
- gnomAD rs745466136
- Stop Gained
- Variant Prioritization Score for Impact Estimate 0.694
- CADD 34.00
- Most common in the REMAINING population (allele frequency 0.0002)
- Structural context available