Related gene-specific medical variations for Gene (Select 105377633) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2263176	NM_003400.4(XPO1):c.2986C>G (p.Leu996Val)	USP34-DT, XPO1 (L996V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257298	NM_003400.4(XPO1):c.3092C>T (p.Ser1031Phe)	USP34-DT, XPO1 (S1031F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 748180	NM_003400.4(XPO1):c.2812+7A>T	USP34-DT, XPO1	Single nucleotide variant (intron variant)	not provided	GLikely benign

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