P51H (p.Pro51His) variant of SDHAF2 (Q9NX18)
P51H (p.Pro51His) in SDHAF2 (Q9NX18) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
P51H (p.Pro51His) variant details
- p.Pro51His
- NCI-TCGA Cosmic COSV1000
- cosmic curated COSV10007
- gnomAD rs1371376884
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available