"GeneReviews"[submitter] AND "MSH6"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 89534	NM_000179.3(MSH6):c.467C>G (p.Ser156Ter)	MSH6 (S156*)	Single nucleotide variant (nonsense +2 more)	Lynch syndrome	GPathogenic
Select item 8932	NM_000179.3(MSH6):c.651dup (p.Lys218Ter)	MSH6 (K88* +1 more)	Duplication (nonsense +1 more)	Lynch syndrome	GPathogenic
Select item 89189	NM_000179.3(MSH6):c.1346T>C (p.Leu449Pro)	MSH6 (L449P +2 more)	Single nucleotide variant (missense variant)	Lynch syndrome	GPathogenic
Select item 89206	NM_000179.3(MSH6):c.1614_1615delinsAG (p.Tyr538_Leu539delinsTer)	MSH6	Indel (nonsense)	Lynch syndrome	GPathogenic
Select item 89323	NM_000179.3(MSH6):c.2931C>G (p.Tyr977Ter)	MSH6 (Y977* +2 more)	Single nucleotide variant (nonsense)	Lynch syndrome	GPathogenic
Select item 89328	NM_000179.3(MSH6):c.2983G>T (p.Glu995Ter)	MSH6 (E995* +2 more)	Single nucleotide variant (nonsense)	Lynch syndrome	GPathogenic
Select item 89488	NM_000179.3(MSH6):c.3959_3962del (p.Ala1320fs)	MSH6 (A1190fs +1 more)	Deletion (frameshift variant)	Lynch syndrome	GPathogenic
Select item 89496	NM_000179.3(MSH6):c.3984_3987dup (p.Leu1330fs)	MSH6 (L1200fs +2 more)	Duplication (frameshift variant)	Lynch syndrome	GPathogenic

ClinVar