ALOX5[gene] and "single gene"[properties] - ClinVar

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Items: 36

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 14446	NC_000010.11:g.45374102GGGGGC[2]	ALOX5	Microsatellite	Asthma, diminished response to antileukotriene treatment in +1 more	Gdrug response; risk factor
Select item 2456834	NM_000698.5(ALOX5):c.64A>G (p.Ile22Val)	ALOX5 (I22V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2268605	NM_000698.5(ALOX5):c.89C>T (p.Ala30Val)	ALOX5 (A30V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 760574	NM_000698.5(ALOX5):c.210C>T (p.Ile70=)	ALOX5	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 738796	NM_000698.5(ALOX5):c.237C>T (p.Asp79=)	ALOX5	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2474027	NM_000698.5(ALOX5):c.302A>G (p.Tyr101Cys)	ALOX5 (Y101C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 713947	NM_000698.5(ALOX5):c.318C>T (p.Gly106=)	ALOX5	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2558418	NM_000698.5(ALOX5):c.341A>C (p.Asp114Ala)	ALOX5 (D114A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2248112	NM_000698.5(ALOX5):c.347G>A (p.Arg116His)	ALOX5 (R116H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2329798	NM_000698.5(ALOX5):c.354G>T (p.Lys118Asn)	ALOX5 (K118N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3112899	NM_000698.5(ALOX5):c.362G>A (p.Arg121Gln)	ALOX5 (R121Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3112903	NM_000698.5(ALOX5):c.377A>G (p.His126Arg)	ALOX5 (H126R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 741995	NM_000698.5(ALOX5):c.397C>T (p.Arg133Cys)	ALOX5 (R133C)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 3112906	NM_000698.5(ALOX5):c.398G>A (p.Arg133His)	ALOX5 (R133H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2455095	NM_000698.5(ALOX5):c.415C>T (p.Arg139Trp)	ALOX5 (R139W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2282615	NM_000698.5(ALOX5):c.473C>A (p.Ala158Asp)	ALOX5 (A13D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 221317	NM_000698.5(ALOX5):c.490T>G (p.Leu164Val)	ALOX5 (L164V +1 more)	Single nucleotide variant (missense variant)	Breast ductal adenocarcinoma	GUncertain significance
Select item 3288127	NM_000698.5(ALOX5):c.497G>A (p.Arg166His)	ALOX5 (R166H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372412	NM_000698.5(ALOX5):c.570C>G (p.Phe190Leu)	ALOX5 (F45L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112915	NM_000698.5(ALOX5):c.674A>G (p.Asn225Ser)	ALOX5 (N80S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112917	NM_000698.5(ALOX5):c.806G>A (p.Arg269Gln)	ALOX5 (R124Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 770765	NM_000698.5(ALOX5):c.855G>A (p.Val285=)	ALOX5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3112921	NM_000698.5(ALOX5):c.880G>A (p.Asp294Asn)	ALOX5 (D149N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288107	NM_000698.5(ALOX5):c.897C>A (p.Asp299Glu)	ALOX5 (D154E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258987	NM_000698.5(ALOX5):c.922G>A (p.Ala308Thr)	ALOX5 (A308T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 788565	NM_000698.5(ALOX5):c.981+9C>T	ALOX5	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 120088	NM_000698.5(ALOX5):c.996G>A (p.Pro332=)	ALOX5	Single nucleotide variant (synonymous variant)	not provided	Gnot provided
Select item 2271962	NM_000698.5(ALOX5):c.1003G>A (p.Glu335Lys)	ALOX5 (E335K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 120087	NM_000698.5(ALOX5):c.1273-34C>T	ALOX5	Single nucleotide variant (intron variant)	not provided	Gnot provided
Select item 3288100	NM_000698.5(ALOX5):c.1340C>T (p.Ala447Val)	ALOX5 (A302V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2481266	NM_000698.5(ALOX5):c.1385G>A (p.Ser462Asn)	ALOX5 (S433N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288139	NM_000698.5(ALOX5):c.1409T>A (p.Phe470Tyr)	ALOX5 (F438Y +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2246707	NM_000698.5(ALOX5):c.1426C>T (p.Leu476Phe)	ALOX5 (L447F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463148	NM_000698.5(ALOX5):c.1427T>A (p.Leu476His)	ALOX5 (L447H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220458	NM_000698.5(ALOX5):c.1669G>A (p.Gly557Ser)	ALOX5 (G525S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355792	NM_000698.5(ALOX5):c.1744G>A (p.Val582Met)	ALOX5 (V437M +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 36