N26D (p.Asn26Asp) variant of RAC1 (P63000)
N26D (p.Asn26Asp) in RAC1 (P63000) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.70 / 1. The record also includes structural context.
N26D (p.Asn26Asp) variant details
- p.Asn26Asp
- rs2115193158
- NCI-TCGA Cosmic COSV6182
- cosmic curated COSV61822
- UniProt VAR 014540
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.705
- AlphaMissense 0.90
- MetaLR 0.66
- MetaSVM 0.56
- PolyPhen-2 1.00
- SIFT 0.00
- EVE 0.64
- UniProt: Variant assessed as somatic; moderate impact. (in dbSNP:rs2115193158)
- Structural context available