ENO1[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 722451	NM_001428.5(ENO1):c.1305A>G (p.Ter435=)	ENO1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2237618	NM_001428.5(ENO1):c.1280A>G (p.Asn427Ser)	ENO1 (N334S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510847	NM_001428.5(ENO1):c.1270G>C (p.Ala424Pro)	ENO1 (A331P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3088895	NM_001428.5(ENO1):c.1252G>A (p.Gly418Ser)	ENO1 (G325S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3088898	NM_001428.5(ENO1):c.999C>A (p.Asn333Lys)	ENO1 (N240K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294619	NM_001428.5(ENO1):c.896A>G (p.Asp299Gly)	ENO1 (D299G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285942	NM_001428.5(ENO1):c.874A>G (p.Ile292Val)	ENO1 (I292V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3088897	NM_001428.5(ENO1):c.860A>C (p.Tyr287Ser)	ENO1 (Y194S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275163	NM_001428.5(ENO1):c.806G>T (p.Arg269Met)	ENO1 (R176M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 775127	NM_001428.5(ENO1):c.735C>T (p.Asp245=)	ENO1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 751845	NM_001428.5(ENO1):c.668-10C>T	ENO1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2535108	NM_001428.5(ENO1):c.649A>G (p.Ile217Val)	ENO1 (I124V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222591	NM_001428.5(ENO1):c.547C>T (p.Arg183Cys)	ENO1 (R183C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384027	NM_001428.5(ENO1):c.316T>G (p.Phe106Val)	ENO1 (F13V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510758	NM_001428.5(ENO1):c.175G>A (p.Gly59Arg)	ENO1 (G59R)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 731576	NM_001428.5(ENO1):c.162G>A (p.Lys54=)	ENO1	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 3088896	NM_001428.5(ENO1):c.131A>G (p.Tyr44Cys)	ENO1 (Y44C)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2611138	NM_001428.5(ENO1):c.101C>G (p.Ala34Gly)	ENO1 (A34G)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2307714	NM_001428.5(ENO1):c.98C>G (p.Ala33Gly)	ENO1 (A33G)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance