Related gene-specific medical variations for Gene (Select 23220) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3273983	NM_015177.2(DTX4):c.113C>T (p.Pro38Leu)	DTX4, LOC130005742 (P38L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2323868	NM_015177.2(DTX4):c.43G>A (p.Glu15Lys)	DTX4, LOC121392917 (E15K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1690327	NM_015177.2(DTX4):c.974G>A (p.Ser325Asn)	DTX4 (S219N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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