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Gene Protein AA change dbSNP Phenotype Chain Detail
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1 MECP2 P51608 p.Arg306Ser rs28935468 RETT SYNDROME [MIM:300005#0016]
Detail
0.74 (T)
0.996 (D)
N
2 MECP2 P51608 p.Arg306Cys rs28935468 Rett syndrome (RTT) [MIM:312750]
Detail
0.05 (T)
1 (D)
N
3 MECP2 P51608 p.Arg306Gly rs28935468 RETT SYNDROME [MIM:300005#0016]
Detail
0.38 (T)
0.996 (D)
N