"PreventionGenetics, part of Exact Sciences"[submitter] AND "MUC1"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3061706	NM_002456.6(MUC1):c.800C>G (p.Ala267Gly)	MUC1 (A1224G +17 more)	Single nucleotide variant (missense variant +1 more)	MUC1-related disorder	GUncertain significance
Select item 3036300	NM_002456.6(MUC1):c.628G>A (p.Gly210Arg)	MUC1 (G114R +20 more)	Single nucleotide variant (missense variant)	MUC1-related disorder	GUncertain significance
Select item 1049509	NM_001204288.2(MUC1):c.493G>A (p.Gly165Ser)	MUC1 (G104S +1 more)	Single nucleotide variant (synonymous variant +2 more)	MUC1-related disorder	GUncertain significance
Select item 3036365	NM_002456.6(MUC1):c.468C>T (p.Asp156=)	MUC1	Single nucleotide variant (synonymous variant +1 more)	MUC1-related disorder	GLikely benign
Select item 3052067	NM_002456.6(MUC1):c.459G>A (p.Thr153=)	MUC1	Single nucleotide variant (synonymous variant +1 more)	MUC1-related disorder	GLikely benign
Select item 2635023	NM_002456.6(MUC1):c.367C>G (p.Leu123Val)	MUC1 (L105V +11 more)	Single nucleotide variant (missense variant +1 more)	MUC1-related disorder	GUncertain significance
Select item 2630759	NM_002456.6(MUC1):c.151_159+5del	MUC1 (K51fs +1 more)	Deletion (frameshift variant +1 more)	MUC1-related disorder	GUncertain significance
Select item 3051173	NM_002456.6(MUC1):c.31C>T (p.Leu11=)	MUC1	Single nucleotide variant (synonymous variant)	MUC1-related disorder	GLikely benign

ClinVar