N4D (p.Asn4Asp) variant of SRC (P12931)
N4D (p.Asn4Asp) in SRC (P12931) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data, experimental measurements, published literature, and structural context.
N4D (p.Asn4Asp) variant details
- p.Asn4Asp
- gnomAD 20-37384163-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.321
- REVEL 0.15
- MetaLR 0.19
- MetaSVM -0.91
- CADD 22.50
- PolyPhen-2 0.00
- SIFT 0.02
- Population evidence available
- Structural context available
- SRC SH3 domain domainome 1.0: score -0.384
- Literature evidence available