R27G (p.Arg27Gly) variant of TBK1 (Q9UHD2)
R27G (p.Arg27Gly) in TBK1 (Q9UHD2) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Frontotemporal dementia and/or amyotrophic lateral sclerosis 4. The record also includes published literature and structural context.
R27G (p.Arg27Gly) variant details
- p.Arg27Gly
- rs2539476741
- ClinGen CA385593148
- ClinVar RCV002820866
- Uncertain significance
- Frontotemporal dementia and/or amyotrophic lateral sclerosis 4
- Missense
- ClinVar: Uncertain significance (Frontotemporal dementia and/or amyotrophic lateral sclerosis 4)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- Cited in: Amyotrophic Lateral Sclerosis Overview. (PMID 20301623)