T17A (p.Thr17Ala) variant of NLGN3 (Neuroligin-3)
T17A (p.Thr17Ala) in NLGN3 (Neuroligin-3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data, published literature, and structural context.
T17A (p.Thr17Ala) variant details
- p.Thr17Ala
- gnomAD X-71147798-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.0894
- REVEL 0.03
- CADD 4.77
- PolyPhen-2 0.00
- SIFT 0.58
- Most common in the Non-Finnish European population (allele frequency 1.2e-06)
- Structural context available
- Literature evidence available