P16S (p.Pro16Ser) variant of DNAJC6 (Auxilin)
P16S (p.Pro16Ser) in DNAJC6 (Auxilin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.61 / 1. The record also includes population frequency data, published literature, and structural context.
P16S (p.Pro16Ser) variant details
- p.Pro16Ser
- rs867192361
- gnomAD 1-65254592-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.61
- CADD 17.10
- SIFT 0.20
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- Literature evidence available