P78L (p.Pro78Leu) variant of NLGN3 (Neuroligin-3)
P78L (p.Pro78Leu) in NLGN3 (Neuroligin-3) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.83 / 1. The record also includes population frequency data and structural context.
P78L (p.Pro78Leu) variant details
- p.Pro78Leu
- NCI-TCGA Cosmic COSV1007
- NCI-TCGA Cosmic COSV6244
- cosmic curated COSV62445
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.829
- REVEL 0.92
- CADD 25.30
- PolyPhen-2 1.00
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 1.2e-06)
- Structural context available