H39Q (p.His39Gln) variant of TNFAIP3 (P21580)
H39Q (p.His39Gln) in TNFAIP3 (P21580) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and structural context.
H39Q (p.His39Gln) variant details
- p.His39Gln
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.06
- MetaSVM -1.07
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available