Related gene-specific medical variations for Gene (Select 83593) - ClinVar

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Links from Gene

Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3312984	NM_182663.4(RASSF5):c.167C>A (p.Ala56Glu)	LOC129932342, RASSF5 (A56E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312982	NM_182663.4(RASSF5):c.284C>T (p.Pro95Leu)	LOC129932343, RASSF5 (P95L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312981	NM_182663.4(RASSF5):c.1120A>C (p.Ile374Leu)	EIF2D, RASSF5 (I221L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312980	NM_182663.4(RASSF5):c.628G>A (p.Glu210Lys)	EIF2D, RASSF5 (E210K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151945	NM_182663.4(RASSF5):c.968G>A (p.Arg323Gln)	EIF2D, RASSF5 (R170Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151943	NM_182663.4(RASSF5):c.184G>A (p.Ala62Thr)	LOC129932342, RASSF5 (A62T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151942	NM_182663.4(RASSF5):c.178C>G (p.Arg60Gly)	LOC129932342, RASSF5 (R60G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151941	NM_182663.4(RASSF5):c.160C>T (p.Pro54Ser)	LOC129932342, RASSF5 (P54S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151940	NM_182663.4(RASSF5):c.130C>T (p.Leu44Phe)	LOC129932342, RASSF5 (L44F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151939	NM_182663.4(RASSF5):c.110C>T (p.Pro37Leu)	LOC129932342, RASSF5 (P37L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151938	NM_182663.4(RASSF5):c.1097A>C (p.Glu366Ala)	EIF2D, RASSF5 (E213A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2616014	NM_182663.4(RASSF5):c.1019G>A (p.Arg340His)	EIF2D, RASSF5 (R187H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2555789	NM_182663.4(RASSF5):c.1168G>C (p.Asp390His)	EIF2D, RASSF5 (D390H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2552388	NM_182663.4(RASSF5):c.94G>C (p.Glu32Gln)	LOC129932342, RASSF5 (E32Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539720	NM_182663.4(RASSF5):c.145C>A (p.Pro49Thr)	LOC129932342, RASSF5 (P49T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2472096	NM_182663.4(RASSF5):c.1051G>A (p.Asp351Asn)	EIF2D, RASSF5 (D198N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2460149	NM_182663.4(RASSF5):c.818C>T (p.Thr273Ile)	EIF2D, RASSF5 (T273I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455833	NM_182663.4(RASSF5):c.202G>T (p.Gly68Trp)	LOC129932342, RASSF5 (G68W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410999	NM_182663.4(RASSF5):c.167C>G (p.Ala56Gly)	LOC129932342, RASSF5 (A56G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403209	NM_182663.4(RASSF5):c.134G>T (p.Cys45Phe)	LOC129932342, RASSF5 (C45F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383865	NM_182663.4(RASSF5):c.964A>G (p.Lys322Glu)	EIF2D, RASSF5 (K169E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313729	NM_182663.4(RASSF5):c.970A>T (p.Ile324Leu)	EIF2D, RASSF5 (I171L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302778	NM_182663.4(RASSF5):c.112C>G (p.Pro38Ala)	LOC129932342, RASSF5 (P38A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255095	NM_182663.4(RASSF5):c.140C>T (p.Pro47Leu)	LOC129932342, RASSF5 (P47L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235190	NM_182663.4(RASSF5):c.662G>A (p.Arg221Gln)	EIF2D, RASSF5 (R68Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Links from Gene

Items: 25