The UMD-APC mutations database
Mutation c.1690C>T



     Data for this mutation

Co occurence of MLH1, MSH2, MSH6, MUTYH and APC mutations (Pathogenic mutations, Unclassified variants, Non-pathogenic variation)
Sample IDAPCMLH1MSH2MSH6MUTYH
10_APC-012---120P-----
10_APC-012---53P-----
10_APC-177---2615P-----
19_16263---16263.001-----
19_27839---27839.001-----
19_27839---27839.002-----
33_PSL490---06-297-----
33_PSL490---06-298-----
37_P07.08-E602957282-----
37_P07.08-E603057283-----
37_P07.08-E603257284-----
37_P07.08-E603857294-----
37_P98.02209--------
37_P98.16210--------
4_39886---39886-----
7_-6491ILP0612119--------
7_-6491ILP0612120E070252-----
7_-6491ILP0612121--------
SO-2890-----------
SO_-1321G00563G00563-----
SO_-14116116-----
SO_-1438943894-----
SO_-1438953895-----
SO_-1439773977-----
SO_-1439783978-----
SO_-1440054005-----
SO_-14G01368G01368-----
SO_-14G03191G03191-----
SO_-175G02115G02115-----
SO_-175G08058G08058-----
SO_-1851G00589G00589-----
SO_-2101G00846G00846-----
SO_-226616616-----
SO_-226G04128G04128-----
SO_-2440G01808G01808-----
SO_-5710G08943G08943-----
SO_-972G00878G00878-----
SO_-972G01252G01252-----
SO_-972G04819G04819-----
SO_-972G05070G05070-----

Biological significanceDate Comment
Causal28/05/14---