A36T (p.Ala36Thr) variant of CHRNA4 (P43681)
A36T (p.Ala36Thr) in CHRNA4 (P43681) 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 0.51 / 1. The record also includes population frequency data.
A36T (p.Ala36Thr) variant details
- p.Ala36Thr
- NCI-TCGA Cosmic COSV1009
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.509
- REVEL 0.43
- CADD 22.10
- PolyPhen-2 0.14
- SIFT 0.07
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)