A67T (p.Ala67Thr) variant of GNAT1 (P11488)
A67T (p.Ala67Thr) in GNAT1 (P11488) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data and structural context.
A67T (p.Ala67Thr) variant details
- p.Ala67Thr
- cosmic curated COSV10872
- Missense
- Variant Prioritization Score for Impact Estimate 0.405
- REVEL 0.25
- CADD 22.20
- PolyPhen-2 0.00
- SIFT 0.28
- Most common in the Non-Finnish European population (allele frequency 8.8e-05)
- Structural context available