"Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Child - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 218756	NM_018406.7(MUC4):c.9239C>T (p.Ser3080Leu)	MUC4 (S3080L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GBenign
Select item 218755	NM_018406.7(MUC4):c.8510T>G (p.Ile2837Ser)	MUC4 (I2837S)	Single nucleotide variant (no sequence alteration +2 more)	not specified	GBenign
Select item 218754	NM_018406.7(MUC4):c.7349C>T (p.Pro2450Leu)	MUC4 (P2450L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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ClinVar