V49G (p.Val49Gly) variant of TBK1 (Q9UHD2)
V49G (p.Val49Gly) in TBK1 (Q9UHD2) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The record also includes structural context.
V49G (p.Val49Gly) variant details
- p.Val49Gly
- rs2040531971
- ClinGen CA385594453
- ClinVar RCV001310999
- Ensembl rs2040531971
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available