R6S (p.Arg6Ser) variant of FGFR2 (P21802)
R6S (p.Arg6Ser) in FGFR2 (P21802) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
R6S (p.Arg6Ser) variant details
- p.Arg6Ser
- 1000Genomes rs141724446
- ESP rs141724446
- ExAC rs141724446
- TOPMed rs141724446
- Likely benign
- Missense
- EBI: Likely benign (in dbSNP:rs3750819)
- UniProt: Likely benign (in dbSNP:rs3750819)
- Structural context available