S36G (p.Ser36Gly) variant of ADAMTS13 (Q76LX8)
S36G (p.Ser36Gly) in ADAMTS13 (Q76LX8) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data and structural context.
S36G (p.Ser36Gly) variant details
- p.Ser36Gly
- gnomAD rs1554784004
- Missense
- Variant Prioritization Score for Impact Estimate 0.149
- REVEL 0.10
- MetaLR 0.37
- MetaSVM -0.80
- CADD 7.16
- PolyPhen-2 0.15
- SIFT 0.48
- Most common in the Non-Finnish European population (allele frequency 4.5e-06)
- Structural context available