The UMD-MSH2 mutations database
Mutation c.IVS8+104C>T (c.1386+104C>T)

     Data for this mutation

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

Sample ID	MSH2	MLH1	MSH6	MUTYH	APC
2_02-ACT1924_14855_14855	-	-	-	-	-
2_02-ACT2098_15121_15121	-	-	-	-	-
2_02-ACT2324_15652_15652	-	-	-	-	-
2_HEGP-HNPCC169 EXT87_190	-	-	-	-	-

Complementary data about this mutation

Analysis	Result	Date	Origin	PMID/dbSNP
Allele frequency	rs17224444 : 2.3%heterozygotes, 0% homozygotes TT (PDR90 population)	28/02/12	dbSNP	rs17224444

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