EDN2[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2544112	NM_001956.5(EDN2):c.520A>G (p.Arg174Gly)	EDN2 (R141G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3087200	NM_001956.5(EDN2):c.501G>T (p.Glu167Asp)	EDN2 (E167D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3087199	NM_001956.5(EDN2):c.496C>T (p.Arg166Trp)	EDN2 (R166W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2529792	NM_001956.5(EDN2):c.422G>A (p.Gly141Glu)	EDN2 (G141E)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2514050	NM_001956.5(EDN2):c.355G>C (p.Gly119Arg)	EDN2 (G119R)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 716660	NM_001956.5(EDN2):c.345-4G>A	EDN2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3087197	NM_001956.5(EDN2):c.313G>A (p.Ala105Thr)	EDN2 (A105T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2609856	NM_001956.5(EDN2):c.292T>C (p.Cys98Arg)	EDN2 (C98R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2472166	NM_001956.5(EDN2):c.116C>T (p.Ala39Val)	EDN2 (A39V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589486	NM_001956.5(EDN2):c.49G>A (p.Val17Met)	EDN2 (V17M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance