M99R (p.Met99Arg) variant of SLC2A1 (P11166)
M99R (p.Met99Arg) in SLC2A1 (P11166) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as likely pathogenic in the context of not provided. The record also includes structural context.
M99R (p.Met99Arg) variant details
- p.Met99Arg
- rs2524998344
- ClinGen CA339961367
- ClinVar RCV003239128
- Likely pathogenic
- not provided
- Missense
- ClinVar: Likely pathogenic (not provided)
- EBI: Likely pathogenic
- UniProt: Likely pathogenic
- Structural context available