P17Q (p.Pro17Gln) variant of MYC (Myc proto-oncogene protein)
P17Q (p.Pro17Gln) in MYC (Myc proto-oncogene protein) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data, published literature, and structural context.
P17Q (p.Pro17Gln) variant details
- p.Pro17Gln
- rs1027454697
- gnomAD 8-127736095-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.156
- CADD 3.26
- SIFT 0.31
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available
- Literature evidence available