P16Q (p.Pro16Gln) variant of DNAJC6 (Auxilin)
P16Q (p.Pro16Gln) in DNAJC6 (Auxilin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data, published literature, and structural context.
P16Q (p.Pro16Gln) variant details
- p.Pro16Gln
- rs1376257471
- gnomAD 1-65254593-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.268
- CADD 15.10
- SIFT 0.06
- Most common in the Non-Finnish European population (allele frequency 7.4e-05)
- Structural context available
- Literature evidence available