A15D (p.Ala15Asp) variant of SDHAF2 (Q9NX18)
A15D (p.Ala15Asp) in SDHAF2 (Q9NX18) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A15D (p.Ala15Asp) variant details
- p.Ala15Asp
- NCI-TCGA Cosmic COSV5709
- cosmic curated COSV57099
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available