Related gene-specific medical variations for Gene (Select 10071) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2657832	NM_001164462.2(MUC12):c.16005G>A (p.Val5335=)	LOC123956190, MUC12	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2657831	NM_001164462.2(MUC12):c.15972C>T (p.His5324=)	LOC123956190, MUC12	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 156706	NM_001164462.2(MUC12):c.8611G>A (p.Ala2871Thr)	MUC12 (A2871T)	Single nucleotide variant (missense variant)	not provided	Gnot provided

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