A34T (p.Ala34Thr) variant of SRC (P12931)
A34T (p.Ala34Thr) in SRC (P12931) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data, experimental measurements, and structural context.
A34T (p.Ala34Thr) variant details
- p.Ala34Thr
- rs1288993928
- NCI-TCGA Cosmic COSV6243
- cosmic curated COSV62439
- 1000Genomes rs1288993928
- Uncertain significance
- Missense
- Variant Prioritization Score for Impact Estimate 0.115
- REVEL 0.13
- CADD 3.09
- PolyPhen-2 0.00
- SIFT 0.77
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Population evidence available
- Structural context available
- SRC SH3 domain domainome 1.0: score 0.0404