"Department of Human Genetics, Hannover Medical School"[submitter] AND - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 420921	NM_000249.4(MLH1):c.91G>A (p.Ala31Thr)	MLH1 (A31T)	Single nucleotide variant (missense variant +1 more)	Colorectal cancer, hereditary nonpolyposis, type 2 +5 more	GUncertain significance
Select item 3061924	NM_000249.4(MLH1):c.108dup (p.Glu37Ter)	MLH1 (E37*)	Duplication (nonsense +1 more)	Colorectal cancer, hereditary nonpolyposis, type 2	GPathogenic
Select item 182520	NM_000249.4(MLH1):c.790C>G (p.His264Asp)	MLH1 (H264D +3 more)	Single nucleotide variant (missense variant +2 more)	not provided +5 more	GConflicting classifications of pathogenicity
Select item 3257720	NM_000249.4(MLH1):c.1789T>A (p.Trp597Arg)	MLH1 (W356R +5 more)	Single nucleotide variant (missense variant +1 more)	Colorectal cancer, hereditary nonpolyposis, type 2	GUncertain significance
Select item 3061744	NM_000249.4(MLH1):c.1871dup (p.Asp624fs)	MLH1 (D266fs +5 more)	Duplication (frameshift variant +1 more)	Colorectal cancer, hereditary nonpolyposis, type 2	GPathogenic
Select item 3343966	NM_000249.4(MLH1):c.2144_2150del (p.Thr715fs)	MLH1 (T357fs +8 more)	Deletion (frameshift variant)	Colorectal cancer, hereditary nonpolyposis, type 2	GLikely pathogenic

ClinVar