H145Y (p.His145Tyr) variant of STAT6 (P42226)
H145Y (p.His145Tyr) in STAT6 (P42226) 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 0.13 / 1. The record also includes population frequency data and structural context.
H145Y (p.His145Tyr) variant details
- p.His145Tyr
- NCI-TCGA Cosmic COSV1002
- cosmic curated COSV10027
- gnomAD rs2034304576
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.126
- REVEL 0.05
- CADD 5.42
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available