C86S (p.Cys86Ser) variant of TNFRSF13B (O14836)
C86S (p.Cys86Ser) in TNFRSF13B (O14836) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The available variant effect predictions contribute to a CATVariant prioritization score of 0.88 / 1.
C86S (p.Cys86Ser) variant details
- p.Cys86Ser
- rs1597661284
- ClinGen CA398520134
- ClinVar RCV000996501
- Ensembl rs1597661284
- Uncertain significance
- not provided
- Missense
- Variant Prioritization Score for Impact Estimate 0.878
- AlphaMissense 0.95
- MetaLR 0.92
- MetaSVM 0.65
- PolyPhen-2 1.00
- SIFT 0.00
- EVE 0.85
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance