R38G (p.Arg38Gly) variant of PIK3CA (P42336)
R38G (p.Arg38Gly) in PIK3CA (P42336) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance in the context of in CRC. The record also includes structural context.
R38G (p.Arg38Gly) variant details
- p.Arg38Gly
- cosmic curated COSV55892
- ExAC rs749415085
- gnomAD rs749415085
- Uncertain significance
- in CRC
- Missense
- EBI: Variant of uncertain significance (in CRC)
- UniProt: Uncertain significance (in CRC)
- Structural context available