S29N (p.Ser29Asn) variant of SLC25A14 (O95258)
S29N (p.Ser29Asn) in SLC25A14 (O95258) 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 0.34 / 1. The record also includes population frequency data and structural context.
S29N (p.Ser29Asn) variant details
- p.Ser29Asn
- NCI-TCGA Cosmic COSV5442
- cosmic curated COSV54420
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.344
- REVEL 0.20
- ESM-1b 0.00
- AlphaMissense 0.09
- MetaLR 0.22
- MetaSVM -0.81
- CADD 20.50
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the REMAINING population (allele frequency 3.3e-05)
- Structural context available