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Mutations on the Protein: P40692 From Positions: 38 To 76

17
13
0
4


Swiss-Prot Disease: VAR_004441
p.ARG69LYS
N/A
N/A
Hereditary non-polyposis colorectal cancer 2 (HNPCC2)


Swiss-Prot Disease: VAR_043389
p.ASN38HIS
N/A
N/A
Hereditary non-polyposis colorectal cancer 2 (HNPCC2)


Swiss-Prot Disease: VAR_004438
p.ASN64SER
N/A
N/A
Hereditary non-polyposis colorectal cancer 2 (HNPCC2)


Swiss-Prot Disease: VAR_043392
p.ASP63GLU
N/A
N/A
Hereditary non-polyposis colorectal cancer 2 (HNPCC2)


Swiss-Prot Disease: VAR_043390
p.ASP41GLY
N/A
N/A
Hereditary non-polyposis colorectal cancer 2 (HNPCC2)


Swiss-Prot Polymorphism: VAR_054522
p.ASP41HIS
N/A
N/A
N/A


Swiss-Prot Disease: VAR_004437
p.GLN62LYS
N/A
N/A
Hereditary non-polyposis colorectal cancer 2 (HNPCC2)


Swiss-Prot Disease: VAR_004439
p.GLY67ARG
N/A
N/A
Hereditary non-polyposis colorectal cancer 2 (HNPCC2)


Swiss-Prot Polymorphism: VAR_012902
p.GLY54GLU
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_038024
p.GLY67GLU
N/A
N/A
N/A


Swiss-Prot Disease: VAR_012903
p.GLY67TRP
N/A
N/A
Hereditary non-polyposis colorectal cancer 2 (HNPCC2)


Swiss-Prot Disease: VAR_004440
p.ILE68ASN
N/A
N/A
Hereditary non-polyposis colorectal cancer 2 (HNPCC2)


Swiss-Prot Disease: VAR_004436
p.SER44PHE
N/A
N/A
Hereditary non-polyposis colorectal cancer 2 (HNPCC2)


OMIM Disease: 120436.0029
p.GLY67GLU
N/A
N/A
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 2


OMIM Disease: 120436.0011
p.GLY67TRP
N/A
N/A
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 2||MISMATCH REPAIR CANCER SYNDROME, INCLUDED


OMIM Disease: 120436.0034
p.LEU73ARG
N/A
N/A
MISMATCH REPAIR CANCER SYNDROME


OMIM Disease: 120436.0002
p.SER44PHE
N/A
N/A
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 2






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