Related gene-specific medical variations for Gene (Select 10048) - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3151466	NM_005493.3(RANBP9):c.337G>A (p.Gly113Ser)	LOC129995826, RANBP9 (G113S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
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 3151461	NM_005493.3(RANBP9):c.184G>C (p.Ala62Pro)	LOC129995827, RANBP9 (A62P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151460	NM_005493.3(RANBP9):c.179T>C (p.Leu60Ser)	LOC129995827, RANBP9 (L60S)	Single nucleotide variant (missense variant)	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 2404119	NM_005493.3(RANBP9):c.151C>T (p.Pro51Ser)	LOC129995827, RANBP9 (P51S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389051	NM_005493.3(RANBP9):c.122T>G (p.Val41Gly)	LOC129995827, RANBP9 (V41G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383706	NM_005493.3(RANBP9):c.2138G>A (p.Arg713Gln)	RANBP9, NOL7 (R713Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2347748	NM_005493.3(RANBP9):c.142G>A (p.Ala48Thr)	LOC129995827, RANBP9 (A48T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328323	NM_005493.3(RANBP9):c.209A>C (p.His70Pro)	LOC129995827, RANBP9 (H70P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315345	NM_005493.3(RANBP9):c.143C>G (p.Ala48Gly)	LOC129995827, RANBP9 (A48G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310560	NM_005493.3(RANBP9):c.100G>C (p.Val34Leu)	LOC129995827, RANBP9 (V34L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258181	NM_005493.3(RANBP9):c.101T>G (p.Val34Gly)	LOC129995827, RANBP9 (V34G)	Single nucleotide variant (missense variant)	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 2225825	NM_005493.3(RANBP9):c.304C>T (p.Pro102Ser)	LOC129995826, RANBP9 (P102S)	Single nucleotide variant (missense variant)	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