The UMD-APC mutations database
Mutation c.IVS8-132G>T (c.934-132G>T)

     Data for this mutation

Co occurence of MLH1, MSH2, MSH6, MUTYH and APC mutations (Pathogenic mutations, Unclassified variants, Non-pathogenic variation)

Sample ID	APC	MLH1	MSH2	MSH6	MUTYH
19_20387---20387-001	-	-	-	-	-
19_20912---20912-001	-	-	-	-	-
19_21484---21484-001	c.7201C>T (p.Leu2401Leu)	-	-	-	-
19_21569---21569-001	-	-	-	-	-
19_21807---21807-001	-	-	-	-	-
19_21938---21938-001	c.IVS1-82A>C (c.136-82A>C)	-	-	-	-
19_22049---22049-001	-	-	-	-	-
19_22207---22207-001	c.3183_3187delACAAA (p.Gln1062X) c.IVS14+54A>C (c.1958+54A>C)	-	-	-	-
19_22256---22256-001	c.2758_2761delAATG (p.Asn920HisfsX34)	-	-	-	-
19_22484---22484-001	c.694C>T (p.Arg232X) c.IVS8-119C>G (c.934-119C>G) c.IVS8-120G>C (c.934-120G>C)	-	-	-	-
19_24119---24119-001	c.IVS8-119C>G (c.934-119C>G) c.IVS8-120G>C (c.934-120G>C)	-	-	-	-

Complementary data about this mutation

Analysis	Result	Date	Origin	PMID/dbSNP
Co-occurrence	APC: c.3183_3187del, p.Gln1062*	19/09/13	19
Co-occurrence	APC: c.3183_3187del, p.Gln1062*	19/12/13	19	---

Biological significance	Date	Comment
Likely Neutral	19/09/13	---