D77G (p.Asp77Gly) variant of NEB (Nebulin)
D77G (p.Asp77Gly) in NEB (Nebulin) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Nemaline myopathy 2. The record also includes variant effect predictions, population frequency data, and published literature.
D77G (p.Asp77Gly) variant details
- p.Asp77Gly
- rs2099795533
- ClinGen CA348794880
- ClinVar RCV003065139
- Ensembl rs2099795533
- Uncertain significance
- Nemaline myopathy 2
- Missense
- REVEL 0.28
- MetaLR 0.05
- MetaSVM -1.14
- CADD 28.70
- PolyPhen-2 1.00
- SIFT 0.06
- ClinVar: Uncertain significance (Nemaline myopathy 2)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the REMAINING population (allele frequency 0.00048)
- Cited in: Clinical utility gene card for: nemaline myopathy. (PMID 22510848)