T17T (p.Thr17Thr) variant of NLGN3 (Neuroligin-3)
T17T (p.Thr17Thr) in NLGN3 (Neuroligin-3) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data, published literature, and structural context.
T17T (p.Thr17Thr) variant details
- p.Thr17Thr
- gnomAD X-71147800-G-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0825
- CADD 0.28
- Most common in the Non-Finnish European population (allele frequency 1.2e-06)
- Structural context available
- Literature evidence available