The UMD-MSH2 mutations database
Mutation c.390_391delGT



     Data for this mutation

Co occurence of MLH1, MSH2, MSH6, MUTYH and APC mutations (Pathogenic mutations, Unclassified variants, Non-pathogenic variation)
Sample IDMSH2MLH1MSH6MUTYHAPC
33_TNN 015_---_97-364-----
37_L06.31_3258_--------
37_L06.31_3258_43853-----
37_L06.31_5061_50477-----
37_L06.31_5062_50682-----
37_L06.31_5063_50478-----
37_L99.07_10435_87974-----
37_L99.07_581_567-----
37_L99.07_806_2025-----
37_L99.07_849_2794-----
37_L99.07_850_2795-----
4_HD25244_19604_1778-----
5_2008462_20084742_AAC930-----
6_605071_200500277_S6969-----
7_-6044---E051174-----
7_-60444487E051174c.IVS1+9C>G (c.211+9C>G)
c.IVS9-9A>T (c.1511-9A>T)
c.IVS10+12G>A (c.1661+12G>A)		c.IVS14-19A>G (c.1668-19A>G)---

Biological significanceDate Comment
Causal21/02/14---