A27T (p.Ala27Thr) variant of SRC (P12931)
A27T (p.Ala27Thr) in SRC (P12931) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data, experimental measurements, and structural context.
A27T (p.Ala27Thr) variant details
- p.Ala27Thr
- cosmic curated COSV62440
- TOPMed rs2070409976
- Missense
- Variant Prioritization Score for Impact Estimate 0.153
- REVEL 0.08
- CADD 12.60
- PolyPhen-2 0.00
- SIFT 0.45
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- SRC SH3 domain domainome 1.0: score -1