Related gene-specific medical variations for Gene (Select 100506713) - ClinVar

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Links from Gene

Items: 66

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3112577	NM_000697.3(ALOX12):c.986C>A (p.Thr329Lys)	ALOX12, ALOX12-AS1 (T329K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112573	NM_000697.3(ALOX12):c.61C>A (p.Arg21Ser)	ALOX12, ALOX12-AS1 (R21S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112569	NM_000697.3(ALOX12):c.571T>C (p.Tyr191His)	ALOX12, ALOX12-AS1 (Y191H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112565	NM_000697.3(ALOX12):c.548T>C (p.Leu183Pro)	ALOX12, ALOX12-AS1 (L183P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112561	NM_000697.3(ALOX12):c.541G>A (p.Gly181Arg)	ALOX12, ALOX12-AS1 (G181R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112547	NM_000697.3(ALOX12):c.341G>A (p.Arg114His)	ALOX12, ALOX12-AS1 (R114H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112534	NM_000697.3(ALOX12):c.223G>A (p.Ala75Thr)	ALOX12, ALOX12-AS1 (A75T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112528	NM_000697.3(ALOX12):c.207C>A (p.His69Gln)	ALOX12, ALOX12-AS1 (H69Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112514	NM_000697.3(ALOX12):c.1853C>T (p.Pro618Leu)	ALOX12, ALOX12-AS1 (P618L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112509	NM_000697.3(ALOX12):c.1816C>G (p.Pro606Ala)	ALOX12, ALOX12-AS1 (P606A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112506	NM_000697.3(ALOX12):c.1799G>A (p.Arg600His)	ALOX12, ALOX12-AS1 (R600H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112498	NM_000697.3(ALOX12):c.1736G>C (p.Gly579Ala)	ALOX12, ALOX12-AS1 (G579A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112485	NM_000697.3(ALOX12):c.1594T>A (p.Cys532Ser)	ALOX12, ALOX12-AS1 (C532S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3112477	NM_000697.3(ALOX12):c.1413T>G (p.Ile471Met)	ALOX12, ALOX12-AS1 (I471M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112472	NM_000697.3(ALOX12):c.1381G>A (p.Ala461Thr)	ALOX12, ALOX12-AS1 (A461T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112466	NM_000697.3(ALOX12):c.1180C>T (p.Arg394Cys)	ALOX12, ALOX12-AS1 (R394C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2647317	NM_000697.3(ALOX12):c.1029A>C (p.Ala343=)	ALOX12, ALOX12-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2647316	NM_000697.3(ALOX12):c.349G>C (p.Gly117Arg)	ALOX12, ALOX12-AS1 (G117R)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2598722	NM_000697.3(ALOX12):c.1619A>G (p.His540Arg)	ALOX12, ALOX12-AS1 (H540R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2592950	NM_000697.3(ALOX12):c.1208C>T (p.Ala403Val)	ALOX12, ALOX12-AS1 (A403V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2566684	NM_000697.3(ALOX12):c.1504A>T (p.Ile502Phe)	ALOX12, ALOX12-AS1 (I502F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537580	NM_000697.3(ALOX12):c.395T>G (p.Leu132Arg)	ALOX12, ALOX12-AS1 (L132R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534154	NM_000697.3(ALOX12):c.1796G>A (p.Arg599His)	ALOX12, ALOX12-AS1 (R599H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514441	NM_000697.3(ALOX12):c.1091C>T (p.Thr364Ile)	ALOX12, ALOX12-AS1 (T364I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2479149	NM_000697.3(ALOX12):c.797A>G (p.Lys266Arg)	ALOX12, ALOX12-AS1 (K266R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2467649	NM_000697.3(ALOX12):c.404G>A (p.Arg135Lys)	ALOX12, ALOX12-AS1 (R135K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398481	NM_000697.3(ALOX12):c.1988T>C (p.Ile663Thr)	ALOX12, ALOX12-AS1 (I663T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394557	NM_000697.3(ALOX12):c.1010C>G (p.Pro337Arg)	ALOX12, ALOX12-AS1 (P337R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392090	NM_000697.3(ALOX12):c.1604C>T (p.Thr535Met)	ALOX12, ALOX12-AS1 (T535M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2381381	NM_000697.3(ALOX12):c.728G>A (p.Arg243His)	ALOX12, ALOX12-AS1 (R243H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322966	NM_000697.3(ALOX12):c.1093C>G (p.His365Asp)	ALOX12, ALOX12-AS1 (H365D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287353	NM_000697.3(ALOX12):c.275T>C (p.Val92Ala)	ALOX12, ALOX12-AS1 (V92A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2261370	NM_000697.3(ALOX12):c.966C>A (p.Asn322Lys)	ALOX12, ALOX12-AS1 (N322K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2230942	NM_000697.3(ALOX12):c.340C>T (p.Arg114Cys)	ALOX12, ALOX12-AS1 (R114C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1294133	NM_000697.3(ALOX12):c.807+102A>G	ALOX12, ALOX12-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1289083	NM_000697.3(ALOX12):c.337+16C>T	ALOX12, ALOX12-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1277668	NM_000697.3(ALOX12):c.338-156G>A	ALOX12, ALOX12-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1276383	NM_000697.3(ALOX12):c.1902G>A (p.Leu634=)	ALOX12, ALOX12-AS1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1269497	NM_000697.3(ALOX12):c.123C>G (p.Pro41=)	ALOX12, ALOX12-AS1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1266618	NM_000697.3(ALOX12):c.808-118G>A	ALOX12, ALOX12-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1263911	NM_000697.3(ALOX12):c.1540+285T>G	ALOX12, ALOX12-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1262104	NM_000697.3(ALOX12):c.542+23G>A	ALOX12, ALOX12-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1262015	NM_000697.3(ALOX12):c.337+98T>G	ALOX12, ALOX12-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1259628	NM_000697.3(ALOX12):c.765G>A (p.Ser255=)	ALOX12, ALOX12-AS1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1259077	NM_000697.3(ALOX12):c.807+25A>T	ALOX12-AS1, ALOX12	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1251805	NM_000697.3(ALOX12):c.1161+228C>T	ALOX12, ALOX12-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1248100	NM_000697.3(ALOX12):c.1541-264T>A	ALOX12, ALOX12-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1247877	NM_000697.3(ALOX12):c.1092T>G (p.Thr364=)	ALOX12, ALOX12-AS1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1245488	NM_000697.3(ALOX12):c.951+200C>T	ALOX12, ALOX12-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1244882	NM_000697.3(ALOX12):c.1418+32_1418+33del	ALOX12, ALOX12-AS1	Deletion (intron variant)	not provided	GBenign
Select item 1238555	NM_000697.3(ALOX12):c.1248+241G>A	ALOX12, ALOX12-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1238014	NM_000697.3(ALOX12):c.1418+32C>T	ALOX12, ALOX12-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1235859	NM_000697.3(ALOX12):c.135+58C>T	ALOX12, ALOX12-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1234828	NM_000697.3(ALOX12):c.1452A>G (p.Gln484=)	ALOX12, ALOX12-AS1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1233269	NM_000697.3(ALOX12):c.965A>G (p.Asn322Ser)	ALOX12, ALOX12-AS1 (N322S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1230948	NM_000697.3(ALOX12):c.1540+282A>G	ALOX12, ALOX12-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1224924	NM_000697.3(ALOX12):c.337+37T>C	ALOX12, ALOX12-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1224614	NM_000697.3(ALOX12):c.782A>G (p.Gln261Arg)	ALOX12, ALOX12-AS1 (Q261R)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1222883	NM_000697.3(ALOX12):c.1541-20G>A	ALOX12, ALOX12-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1220801	NM_000697.3(ALOX12):c.136-69G>A	ALOX12, ALOX12-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1182711	NM_000697.3(ALOX12):c.135+160T>C	ALOX12-AS1, ALOX12	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1179701	NM_000697.3(ALOX12):c.951+146G>A	ALOX12, ALOX12-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1178469	NM_000697.3(ALOX12):c.646+84T>C	ALOX12-AS1, ALOX12	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 791340	NM_000697.3(ALOX12):c.566G>A (p.Arg189His)	ALOX12, ALOX12-AS1 (R189H)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 783067	NM_000697.3(ALOX12):c.1211G>A (p.Arg404Gln)	ALOX12, ALOX12-AS1 (R404Q)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 714724	NM_000697.3(ALOX12):c.1289G>A (p.Arg430His)	ALOX12-AS1, ALOX12 (R430H)	Single nucleotide variant (missense variant)	not provided	GBenign

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Links from Gene

Items: 66