T79A (p.Thr79Ala) variant of CSF1R (P07333)
T79A (p.Thr79Ala) 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 0.62 / 1. The record also includes population frequency data.
T79A (p.Thr79Ala) variant details
- p.Thr79Ala
- rs1014062385
- NCI-TCGA Cosmic COSV9964
- TOPMed rs1014062385
- gnomAD rs1014062385
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.615
- CADD 23.30
- PolyPhen-2 0.93
- SIFT 0.01
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the African/African-American population (allele frequency 3e-05)