Related gene-specific medical variations for Gene (Select 51406) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3151464	NM_005493.3(RANBP9):c.2155T>G (p.Cys719Gly)	NOL7, RANBP9 (C719G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3151463	NM_005493.3(RANBP9):c.2021G>A (p.Arg674Lys)	NOL7, RANBP9 (R674K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2610103	NM_005493.3(RANBP9):c.1920G>C (p.Lys640Asn)	NOL7, RANBP9 (K640N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2513306	NM_005493.3(RANBP9):c.1864C>A (p.His622Asn)	NOL7, RANBP9 (H622N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2383706	NM_005493.3(RANBP9):c.2138G>A (p.Arg713Gln)	NOL7, RANBP9 (R713Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2238156	NM_005493.3(RANBP9):c.1883A>G (p.Gln628Arg)	NOL7, RANBP9 (Q628R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2205735	NM_005493.3(RANBP9):c.2180A>G (p.Tyr727Cys)	NOL7, RANBP9 (Y727C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar