Y61H (p.Tyr61His) variant of CSF1R (P07333)
Y61H (p.Tyr61His) in CSF1R (P07333) 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 0.16 / 1. The record also includes population frequency data.
Y61H (p.Tyr61His) variant details
- p.Tyr61His
- rs1423864756
- NCI-TCGA Cosmic COSV5382
- cosmic curated COSV53828
- gnomAD rs1423864756
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.156
- CADD 0.47
- PolyPhen-2 0.01
- SIFT 0.55
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the REMAINING population (allele frequency 1.7e-05)