"Ambry Genetics"[submitter] AND "ALOX5"[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 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 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 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 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 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 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 2271962	NM_000698.5(ALOX5):c.1003G>A (p.Glu335Lys)	ALOX5 (E335K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	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 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
Select item 2257748	NM_000698.5(ALOX5):c.1940G>T (p.Ser647Ile)	ALOX5, LOC102724323 (S502I +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393188	NM_000698.5(ALOX5):c.1942G>A (p.Val648Met)	ALOX5, LOC102724323 (V619M +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258731	NM_000698.5(ALOX5):c.1999C>G (p.Arg667Gly)	ALOX5, LOC102724323 (R610G +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516770	NM_000698.5(ALOX5):c.2000G>A (p.Arg667Gln)	ALOX5, LOC102724323 (R522Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 26