"Department of Molecular Diagnostics, Institute of Oncology Ljubljana" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 638665	NM_000179.3(MSH6):c.619G>T (p.Glu207Ter)	MSH6 (E207*)	Single nucleotide variant (nonsense +2 more)	Lynch syndrome 1	GLikely pathogenic
Select item 89559	NM_000179.3(MSH6):c.718C>T (p.Arg240Ter)	MSH6 (R240* +1 more)	Single nucleotide variant (nonsense +1 more)	Lynch syndrome	GPathogenic
Select item 89247	NM_000179.3(MSH6):c.2062_2063del (p.Val688fs)	MSH6 (V558fs +2 more)	Microsatellite (frameshift variant)	Lynch syndrome	GPathogenic
Select item 617773	NM_000179.3(MSH6):c.2092C>T (p.Gln698Ter)	MSH6 (Q698* +2 more)	Single nucleotide variant (nonsense)	Hereditary nonpolyposis colorectal neoplasms +3 more	GPathogenic/Likely pathogenic
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 1493576	NM_000179.3(MSH6):c.3646+5G>A	MSH6	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 617774	NM_000179.3(MSH6):c.3820G>T (p.Glu1274Ter)	MSH6 (E1274* +2 more)	Single nucleotide variant (nonsense)	Lynch syndrome 1 +1 more	GPathogenic/Likely pathogenic

ClinVar