"Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Child - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 41640	NM_000249.4(MLH1):c.637G>A (p.Val213Met)	MLH1 (V213M +2 more)	Single nucleotide variant (missense variant +1 more)	Lynch syndrome	GBenign
Select item 42496	NM_000249.4(MLH1):c.977T>C (p.Val326Ala)	MLH1 (V326A +3 more)	Single nucleotide variant (missense variant +2 more)	Lynch syndrome	GBenign
Select item 36543	NM_000249.4(MLH1):c.1732-19T>A	MLH1	Single nucleotide variant (intron variant)	not provided +6 more	GBenign/Likely benign
Select item 17090	NM_000249.4(MLH1):c.1733A>G (p.Glu578Gly)	MLH1 (E578G +5 more)	Single nucleotide variant (missense variant +1 more)	Lynch syndrome	GBenign
Select item 142658	NM_000249.4(MLH1):c.1775G>C (p.Ser592Thr)	MLH1 (S592T +5 more)	Single nucleotide variant (missense variant +1 more)	not provided +5 more	GConflicting classifications of pathogenicity
Select item 36546	NM_000249.4(MLH1):c.1959G>T (p.Leu653=)	MLH1	Single nucleotide variant (synonymous variant +1 more)	Lynch syndrome	GBenign
Select item 90042	NM_000249.4(MLH1):c.2101C>A (p.Gln701Lys)	MLH1 (Q701K +7 more)	Single nucleotide variant (missense variant +1 more)	Lynch syndrome	GLikely benign
Select item 36547	NM_000249.4(MLH1):c.2152C>T (p.His718Tyr)	MLH1 (H718Y +8 more)	Single nucleotide variant (missense variant)	Lynch syndrome	GBenign

ClinVar