T37T (p.Thr37Thr) variant of SRC (P12931)
T37T (p.Thr37Thr) in SRC (P12931) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data, experimental measurements, published literature, and structural context.
T37T (p.Thr37Thr) variant details
- p.Thr37Thr
- gnomAD 20-37384264-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.156
- CADD 10.60
- Most common in the Non-Finnish European population (allele frequency 9.2e-07)
- Structural context available
- SRC SH3 domain domainome 1.0: score -0.0639
- Literature evidence available