R10C (p.Arg10Cys) variant of SLC18A2 (Q05940)
R10C (p.Arg10Cys) in SLC18A2 (Q05940) 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 0.59 / 1. The record also includes population frequency data and structural context.
R10C (p.Arg10Cys) variant details
- p.Arg10Cys
- cosmic curated COSV10459
- NCI-TCGA Cosmic COSV5368
- cosmic curated COSV53688
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.589
- CADD 26.10
- PolyPhen-2 0.37
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available