"Medical Genetics Laboratory, Umraniye Training and Research Hospital, - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 89552	NM_000179.3(MSH6):c.663A>C (p.Glu221Asp)	MSH6 (E221D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified +6 more	GConflicting classifications of pathogenicity
Select item 428307	NM_000179.3(MSH6):c.1572_1573del (p.Tyr524_Ser525delinsTer)	MSH6	Deletion (nonsense)	not provided +3 more	GPathogenic/Likely pathogenic
Select item 421621	NM_000179.3(MSH6):c.1714C>T (p.Gln572Ter)	MSH6 (Q572* +2 more)	Single nucleotide variant (nonsense)	not provided +3 more	GPathogenic
Select item 89290	NM_000179.3(MSH6):c.2569_2572del (p.Asp857fs)	MSH6 (D727fs +1 more)	Deletion (frameshift variant)	Lynch syndrome	GPathogenic
Select item 89312	NM_000179.3(MSH6):c.2731C>T (p.Arg911Ter)	MSH6 (R911* +2 more)	Single nucleotide variant (nonsense)	Lynch syndrome	GPathogenic
Select item 89357	NM_000179.3(MSH6):c.3226C>T (p.Arg1076Cys)	MSH6 (R1076C +2 more)	Single nucleotide variant (missense variant)	Lynch syndrome 1	GLikely pathogenic
Select item 418871	NM_000179.3(MSH6):c.3732_3735dup (p.Ser1246fs)	MSH6 (S1246fs +2 more)	Duplication (frameshift variant)	Lynch syndrome 5 +4 more	GPathogenic/Likely pathogenic

ClinVar