Related gene-specific medical variations for Gene (Select 10614) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3105583	NM_006460.3(HEXIM1):c.556G>T (p.Ala186Ser)	HEXIM1, HEXIM2-AS1 (A186S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2479023	NM_006460.3(HEXIM1):c.502T>C (p.Tyr168His)	HEXIM1, HEXIM2-AS1 (Y168H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2327172	NM_006460.3(HEXIM1):c.1040G>A (p.Arg347Gln)	HEXIM1, HEXIM2-AS1 (R347Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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