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Mutations on the Protein: P40692 From Positions: 643 To 680

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11
0
1


Swiss-Prot Polymorphism: VAR_043434
p.ARG659GLN
N/A
N/A
N/A


Swiss-Prot Disease: VAR_012929
p.ARG659LEU
N/A
N/A
Hereditary non-polyposis colorectal cancer 2 (HNPCC2)


Swiss-Prot Disease: VAR_004465
p.ARG659PRO
N/A
N/A
Hereditary non-polyposis colorectal cancer 2 (HNPCC2)


Swiss-Prot Polymorphism: VAR_043432
p.ILE655VAL
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_054537
p.PHE656SER
N/A
N/A
N/A


Swiss-Prot Disease: VAR_012928
p.PRO648LEU
N/A
N/A
Hereditary non-polyposis colorectal cancer 2 (HNPCC2)


Swiss-Prot Disease: VAR_043431
p.PRO654LEU
N/A
N/A
Hereditary non-polyposis colorectal cancer 2 (HNPCC2)


Swiss-Prot Disease: VAR_022669
p.PRO648SER
N/A
N/A
Hereditary non-polyposis colorectal cancer 2 (HNPCC2)


Swiss-Prot Polymorphism: VAR_012930
p.THR662PRO
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_054538
p.TRP666ARG
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_043430
p.TYR646CYS
N/A
N/A
N/A


OMIM Disease: 120436.0020
p.PRO648SER
N/A
N/A
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 2||MISMATCH REPAIR CANCER SYNDROME, INCLUDED






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