T37N (p.Thr37Asn) variant of SRC (P12931)
T37N (p.Thr37Asn) in SRC (P12931) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.46 / 1. The record also includes population frequency data, experimental measurements, and structural context.
T37N (p.Thr37Asn) variant details
- p.Thr37Asn
- cosmic curated COSV10969
- Missense
- Variant Prioritization Score for Impact Estimate 0.461
- REVEL 0.24
- CADD 23.60
- PolyPhen-2 0.99
- SIFT 0.10
- Population evidence available
- Structural context available
- SRC SH3 domain domainome 1.0: score -0.0639