Related gene-specific medical variations for Gene (Select 4588) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 161643	NM_005961.3(MUC6):c.4382C>T (p.Thr1461Ile)	MUC6 (T1461I)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 156712	NM_005961.3(MUC6):c.5911C>T (p.Pro1971Ser)	MUC6 (P1971S)	Single nucleotide variant (missense variant)	not provided	Gnot provided
Select item 156711	NM_005961.3(MUC6):c.4577A>T (p.His1526Leu)	MUC6 (H1526L)	Single nucleotide variant (missense variant)	not provided	Gnot provided

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