List of variants reported as not provided for Mismatch repair cancer syndrome 1; Colorectal cancer, hereditary nonpolyposis, type 2

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000249.4(MLH1):c.1489C>T (p.Arg497Trp)	rs200830026	0.00005
NM_000249.4(MLH1):c.299G>A (p.Arg100Gln)	rs63750266	0.00004
NM_000249.4(MLH1):c.808A>G (p.Thr270Ala)	rs371302926	0.00004
NM_000249.4(MLH1):c.1774A>G (p.Ser592Gly)	rs2125984638
NM_000249.4(MLH1):c.649C>A (p.Arg217Ser)	rs4986984

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