L38Q (p.Leu38Gln) variant of TNFRSF13C (Q96RJ3)
L38Q (p.Leu38Gln) in TNFRSF13C (Q96RJ3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data.
L38Q (p.Leu38Gln) variant details
- p.Leu38Gln
- gnomAD rs2077634412
- Missense
- Variant Prioritization Score for Impact Estimate 0.335
- REVEL 0.14
- CADD 24.20
- PolyPhen-2 0.82
- SIFT 0.00
- Most common in the REMAINING population (allele frequency 0.00048)