M11I (p.Met11Ile) variant of PRRT2 (Q7Z6L0)
M11I (p.Met11Ile) in PRRT2 (Q7Z6L0) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data and structural context.
M11I (p.Met11Ile) variant details
- p.Met11Ile
- TOPMed rs1324649260
- gnomAD rs1324649260
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.17
- REVEL 0.11
- CADD 11.70
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Latino/Admixed American population (allele frequency 6.5e-05)
- Structural context available