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Mutations on the Protein: P40692 From Positions: 0 To 38

12
11
0
1



Swiss-Prot Polymorphism: VAR_043386
p.ALA29SER
N/A
N/A
N/A


Swiss-Prot Disease: VAR_043384
p.ALA21VAL
N/A
N/A
Hereditary non-polyposis colorectal cancer 2 (HNPCC2)


Swiss-Prot Disease: VAR_022663
p.ARG18CYS
N/A
N/A
Hereditary non-polyposis colorectal cancer 2 (HNPCC2)


Swiss-Prot Polymorphism: VAR_038023
p.GLY22ALA
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_043383
p.ILE19PHE
N/A
N/A
N/A


Swiss-Prot Disease: VAR_043385
p.ILE25PHE
N/A
N/A
Hereditary non-polyposis colorectal cancer 2 (HNPCC2)


Swiss-Prot Polymorphism: VAR_014876
p.ILE32VAL
N/A
N/A
N/A


Swiss-Prot Disease: VAR_004434
p.MET35ARG
N/A
N/A
Hereditary non-polyposis colorectal cancer 2 (HNPCC2)


Swiss-Prot Disease: VAR_043388
p.MET35ASN
N/A
N/A
Mismatch repair cancer syndrome (MMRCS)


Swiss-Prot Polymorphism: VAR_043387
p.MET35LYS
N/A
N/A
N/A


Swiss-Prot Disease: VAR_004433
p.PRO28LEU
N/A
N/A
Hereditary non-polyposis colorectal cancer 2 (HNPCC2)


OMIM Disease: 120436.0028
p.MET35ASN
N/A
N/A
MISMATCH REPAIR CANCER SYNDROME||COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 2, INCLUDED






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