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Mutations on the Protein: P40692 From Positions: 113 To 151

8
6
0
2


Swiss-Prot Disease: VAR_012908
p.ALA128PRO
N/A
N/A
Hereditary non-polyposis colorectal cancer 2 (HNPCC2)


Swiss-Prot Polymorphism: VAR_022665
p.ASP132HIS
N/A
N/A
N/A


Swiss-Prot Disease: VAR_004446
p.THR117ARG
N/A
N/A
Hereditary non-polyposis colorectal cancer 2 (HNPCC2)


Swiss-Prot Polymorphism: VAR_054525
p.THR116LYS
N/A
N/A
N/A


Swiss-Prot Disease: VAR_004445
p.THR117MET
N/A
N/A
Hereditary non-polyposis colorectal cancer 2 (HNPCC2)


Swiss-Prot Polymorphism: VAR_054526
p.TYR126ASN
N/A
N/A
N/A


OMIM Disease: 120436.0019
p.ASP132HIS
N/A
N/A
COLORECTAL CANCER, SPORADIC, SUSCEPTIBILITY TO


OMIM Disease: 120436.0017
p.THR117MET
N/A
N/A
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 2






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