Entry
Name
Gene
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
Variation
Variation
Variation
Variation
Variation
Variation
Variation
Variation
Variation
Variation
Variation
Variation
Variation
Variation
Variation
Variation
mutation V106M
COSM:
13505
Variation
Variation
mutation R107C
COSM:
13788
Variation
mutation Y129C
COSM:
13633
Variation
Variation
Variation
Variation
Variation
Variation
Variation
Variation
mutation A102V
COSM:
13675
Variation
Variation
Variation
Variation
Variation
Variation
Variation
mutation D116Y
COSM:
13807
Variation
Variation
Variation
mutation D108H
COSM:
13520
Variation
Variation
mutation G111D
COSM:
13508
Variation
Variation
Variation
Variation
Variation
Variation
Variation
mutation E120K COSM:13296
Variation
mutation E120A
COSM:
13614
Network
Disease
H00004 Chronic myeloid leukemia
H00014 Non-small cell lung cancer
Reference
Authors
Foulkes WD, Flanders TY, Pollock PM, Hayward NK
Title
The CDKN2A (p16) gene and human cancer.
Journal
Mol Med 3:5-20 (1997)
Reference
Authors
Freedberg DE, Rigas SH, Russak J, Gai W, Kaplow M, Osman I, Turner F, Randerson-Moor JA, Houghton A, Busam K, Timothy Bishop D, Bastian BC, Newton-Bishop JA, Polsky D
Title
Frequent p16-independent inactivation of p14ARF in human melanoma.
Journal
LinkDB
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