GDE1[gene] and "single gene"[properties] - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3099211	NM_016641.4(GDE1):c.984A>C (p.Glu328Asp)	GDE1 (E218D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3099209	NM_016641.4(GDE1):c.979T>G (p.Cys327Gly)	GDE1 (C217G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2548700	NM_016641.4(GDE1):c.953A>G (p.Tyr318Cys)	GDE1 (Y208C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2312889	NM_016641.4(GDE1):c.923G>C (p.Ser308Thr)	GDE1 (S277T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3099207	NM_016641.4(GDE1):c.869C>T (p.Ser290Leu)	GDE1 (S259L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2220601	NM_016641.4(GDE1):c.826A>T (p.Met276Leu)	GDE1 (M245L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3099206	NM_016641.4(GDE1):c.763A>G (p.Ile255Val)	GDE1 (I145V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2550178	NM_016641.4(GDE1):c.601G>T (p.Val201Leu)	GDE1 (V201L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2255429	NM_016641.4(GDE1):c.472A>G (p.Arg158Gly)	GDE1 (R158G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3099203	NM_016641.4(GDE1):c.436A>G (p.Arg146Gly)	GDE1 (R146G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2235492	NM_016641.4(GDE1):c.328T>G (p.Leu110Val)	GDE1 (L110V)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3099202	NM_016641.4(GDE1):c.190C>G (p.Arg64Gly)	GDE1 (R64G)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3099201	NM_016641.4(GDE1):c.189C>G (p.Asp63Glu)	GDE1 (D63E)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2233346	NM_016641.4(GDE1):c.175C>T (p.Leu59Phe)	GDE1 (L59F)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2316700	NM_016641.4(GDE1):c.135C>A (p.Phe45Leu)	GDE1 (F45L)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2459459	NM_016641.4(GDE1):c.104C>G (p.Thr35Ser)	GDE1 (T35S)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3099208	NM_016641.4(GDE1):c.95G>C (p.Cys32Ser)	GDE1 (C32S)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 768758	NM_016641.4(GDE1):c.93C>G (p.Ala31=)	GDE1	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GBenign
Select item 2326130	NM_016641.4(GDE1):c.80G>A (p.Ser27Asn)	GDE1 (S27N)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3099205	NM_016641.4(GDE1):c.71T>C (p.Val24Ala)	GDE1 (V24A)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance

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Items: 20