A20G (p.Ala20Gly) variant of MSH6 (DNA mismatch repair protein Msh6)
A20G (p.Ala20Gly) in MSH6 (DNA mismatch repair protein Msh6) is a missense change. Clinical records from EBI and UniProt describe it as benign in the context of in LYNCH5, CRC and ENDMC. The record also includes structural context.
A20G (p.Ala20Gly) variant details
- p.Ala20Gly
- 1000Genomes rs63750664
- ESP rs63750664
- ExAC rs63750664
- TOPMed rs63750664
- Benign
- in LYNCH5, CRC and ENDMC
- Missense
- EBI: Benign (in LYNCH5, CRC and ENDMC)
- UniProt: Benign (in LYNCH5, CRC and ENDMC)
- Structural context available