C4552100[trait identifier] AND "GeneID Lab - Advanced Molecular Diagno - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1319971	NM_000179.3(MSH6):c.1453C>T (p.Gln485Ter)	MSH6 (Q183* +2 more)	Single nucleotide variant (nonsense)	Lynch syndrome	GLikely pathogenic
Select item 188181	NM_000179.3(MSH6):c.1498G>A (p.Ala500Thr)	MSH6 (A500T +2 more)	Single nucleotide variant (missense variant)	Hereditary nonpolyposis colorectal neoplasms +3 more	GConflicting classifications of pathogenicity
Select item 1319965	NM_000179.3(MSH6):c.3801+1_3801+2insGTAT	MSH6	Insertion (splice donor variant)	Lynch syndrome	GLikely pathogenic

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