Related gene-specific medical variations for Gene (Select 9125) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 376527	NM_005444.3(CNOT9):c.260C>G (p.Ser87Cys)	CNOT9 (S87C)	Single nucleotide variant (missense variant +1 more)	Prostate adenocarcinoma +4 more	GLikely pathogenic
Select item 376526	NM_005444.3(CNOT9):c.259T>C (p.Ser87Pro)	CNOT9 (S87P)	Single nucleotide variant (missense variant +1 more)	Gastric adenocarcinoma +4 more	GLikely pathogenic
Select item 376525	NM_005444.3(CNOT9):c.391C>T (p.Pro131Ser)	CNOT9 (P131S)	Single nucleotide variant (missense variant)	Malignant melanoma of skin	GLikely pathogenic

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