P16T (p.Pro16Thr) variant of DNAJC6 (Auxilin)
P16T (p.Pro16Thr) in DNAJC6 (Auxilin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.60 / 1. The record also includes population frequency data, published literature, and structural context.
P16T (p.Pro16Thr) variant details
- p.Pro16Thr
- gnomAD 1-65254592-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.602
- CADD 16.70
- SIFT 0.08
- Most common in the South Asian population (allele frequency 2.9e-05)
- Structural context available
- Literature evidence available