HMOX1[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1693775	NM_002133.3(HMOX1):c.-13C>T	HMOX1	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 1163763	NM_002133.3(HMOX1):c.-7C>T	HMOX1	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 2632902	NM_002133.3(HMOX1):c.17C>A (p.Pro6His)	HMOX1 (P6H)	Single nucleotide variant (missense variant)	HMOX1-related condition	GUncertain significance
Select item 2908426	NM_002133.3(HMOX1):c.18C>T (p.Pro6=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1168542	NM_002133.3(HMOX1):c.19G>C (p.Asp7His)	HMOX1 (D7H)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2109104	NM_002133.3(HMOX1):c.21C>G (p.Asp7Glu)	HMOX1 (D7E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2020082	NM_002133.3(HMOX1):c.24-12T>C	HMOX1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2819785	NM_002133.3(HMOX1):c.24-5C>T	HMOX1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2415900	NM_002133.3(HMOX1):c.25A>T (p.Met9Leu)	HMOX1 (M9L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2272591	NM_002133.3(HMOX1):c.25A>C (p.Met9Leu)	HMOX1 (M9L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1489593	NM_002133.3(HMOX1):c.37T>A (p.Leu13Met)	HMOX1 (L13M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2752987	NM_002133.3(HMOX1):c.42A>T (p.Ser14=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2191602	NM_002133.3(HMOX1):c.53A>T (p.Lys18Met)	HMOX1 (K18M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 809355	NM_002133.3(HMOX1):c.55dup (p.Glu19fs)	HMOX1 (E19fs)	Duplication (frameshift variant)	not provided	GLikely pathogenic
Select item 1636790	NM_002133.3(HMOX1):c.54G>A (p.Lys18=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2824188	NM_002133.3(HMOX1):c.57_60dup (p.Thr21fs)	HMOX1 (T21fs)	Duplication (frameshift variant)	not provided	GPathogenic
Select item 2817414	NM_002133.3(HMOX1):c.57G>A (p.Glu19=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2982631	NM_002133.3(HMOX1):c.63C>T (p.Thr21=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1359508	NM_002133.3(HMOX1):c.65A>C (p.Lys22Thr)	HMOX1 (K22T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2719824	NM_002133.3(HMOX1):c.69G>A (p.Glu23=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2708542	NM_002133.3(HMOX1):c.81G>A (p.Gln27=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1423273	NM_002133.3(HMOX1):c.87G>T (p.Glu29Asp)	HMOX1 (E29D)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2971203	NM_002133.3(HMOX1):c.99C>T (p.Phe33=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2978819	NM_002133.3(HMOX1):c.105G>A (p.Arg35=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1552878	NM_002133.3(HMOX1):c.108C>T (p.Asn36=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2814901	NM_002133.3(HMOX1):c.109T>C (p.Phe37Leu)	HMOX1 (F37L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2788489	NM_002133.3(HMOX1):c.117G>A (p.Lys39=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2766313	NM_002133.3(HMOX1):c.120C>G (p.Gly40=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2841541	NM_002133.3(HMOX1):c.129C>A (p.Thr43=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1326850	NM_002133.3(HMOX1):c.130C>T (p.Arg44Ter)	HMOX1 (R44*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 1058925	NM_002133.3(HMOX1):c.131G>A (p.Arg44Gln)	HMOX1 (R44Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2815052	NM_002133.3(HMOX1):c.135_139del (p.Gly46fs)	HMOX1 (G46fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 1595809	NM_002133.3(HMOX1):c.135C>T (p.Asp45=)	HMOX1	Single nucleotide variant (synonymous variant)	HMOX1-related condition +1 more	GLikely benign
Select item 1464608	NM_002133.3(HMOX1):c.136G>A (p.Gly46Ser)	HMOX1 (G46S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2764359	NM_002133.3(HMOX1):c.144+1G>A	HMOX1	Single nucleotide variant (splice donor variant)	not provided	GLikely pathogenic
Select item 1167966	NM_002133.3(HMOX1):c.144+4T>C	HMOX1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2737486	NM_002133.3(HMOX1):c.144+5G>C	HMOX1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2718263	NM_002133.3(HMOX1):c.144+8G>A	HMOX1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3009592	NM_002133.3(HMOX1):c.144+11T>C	HMOX1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2977578	NM_002133.3(HMOX1):c.144+20T>C	HMOX1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1166902	NM_002133.3(HMOX1):c.145-19C>T	HMOX1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2979226	NM_002133.3(HMOX1):c.145-18T>G	HMOX1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1659033	NM_002133.3(HMOX1):c.145-17G>A	HMOX1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1474500	NM_002133.3(HMOX1):c.145-12C>G	HMOX1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2752171	NM_002133.3(HMOX1):c.145-10C>T	HMOX1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3005762	NM_002133.3(HMOX1):c.145-4del	HMOX1	Deletion (intron variant)	not provided	GLikely benign
Select item 3000769	NM_002133.3(HMOX1):c.150G>C (p.Val50=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1520465	NM_002133.3(HMOX1):c.151A>T (p.Met51Leu)	HMOX1 (M51L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2827675	NM_002133.3(HMOX1):c.156C>G (p.Ala52=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2417748	NM_002133.3(HMOX1):c.173A>G (p.Tyr58Cys)	HMOX1 (Y58C)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2028443	NM_002133.3(HMOX1):c.177G>A (p.Val59=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1351980	NM_002133.3(HMOX1):c.204C>G (p.Asn68Lys)	HMOX1 (N68K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2957947	NM_002133.3(HMOX1):c.207G>A (p.Lys69=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2862239	NM_002133.3(HMOX1):c.210G>A (p.Glu70=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1399690	NM_002133.3(HMOX1):c.210G>T (p.Glu70Asp)	HMOX1 (E70D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3004273	NM_002133.3(HMOX1):c.213C>T (p.Ser71=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2091767	NM_002133.3(HMOX1):c.215C>T (p.Pro72Leu)	HMOX1 (P72L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2824386	NM_002133.3(HMOX1):c.219C>T (p.Val73=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2047686	NM_002133.3(HMOX1):c.220T>C (p.Phe74Leu)	HMOX1 (F74L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 710830	NM_002133.3(HMOX1):c.222C>T (p.Phe74=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2990917	NM_002133.3(HMOX1):c.227_228del (p.Pro76fs)	HMOX1 (P76fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 3007963	NM_002133.3(HMOX1):c.228del (p.Val77fs)	HMOX1 (V77fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2985933	NM_002133.3(HMOX1):c.237C>T (p.Phe79=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1542673	NM_002133.3(HMOX1):c.246G>A (p.Glu82=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2893469	NM_002133.3(HMOX1):c.247C>G (p.Leu83Val)	HMOX1 (L83V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2771737	NM_002133.3(HMOX1):c.247C>T (p.Leu83=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1352914	NM_002133.3(HMOX1):c.253C>T (p.Arg85Cys)	HMOX1 (R85C)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1421201	NM_002133.3(HMOX1):c.254G>A (p.Arg85His)	HMOX1 (R85H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1021518	NM_002133.3(HMOX1):c.254G>T (p.Arg85Leu)	HMOX1 (R85L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1594530	NM_002133.3(HMOX1):c.261T>C (p.Ala87=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1326853	NM_002133.3(HMOX1):c.262_268delinsCC (p.Ala88fs)	HMOX1 (A88fs)	Indel (frameshift variant)	not provided	GLikely pathogenic
Select item 1411177	NM_002133.3(HMOX1):c.263C>A (p.Ala88Asp)	HMOX1 (A88D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2708753	NM_002133.3(HMOX1):c.277C>T (p.Leu93=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2749690	NM_002133.3(HMOX1):c.279G>A (p.Leu93=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1655765	NM_002133.3(HMOX1):c.282C>G (p.Ala94=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2836347	NM_002133.3(HMOX1):c.285C>T (p.Phe95=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1318566	NM_002133.3(HMOX1):c.287G>A (p.Trp96Ter)	HMOX1 (W96*)	Single nucleotide variant (nonsense)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2845608	NM_002133.3(HMOX1):c.288G>A (p.Trp96Ter)	HMOX1 (W96*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2843706	NM_002133.3(HMOX1):c.291C>A (p.Tyr97Ter)	HMOX1 (Y97*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 712414	NM_002133.3(HMOX1):c.291C>T (p.Tyr97=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2799543	NM_002133.3(HMOX1):c.294G>A (p.Gly98=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2209238	NM_002133.3(HMOX1):c.298C>T (p.Arg100Cys)	HMOX1 (R100C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1399096	NM_002133.3(HMOX1):c.299G>A (p.Arg100His)	HMOX1 (R100H)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3019075	NM_002133.3(HMOX1):c.300C>A (p.Arg100=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2841479	NM_002133.3(HMOX1):c.303_328del (p.Trp101fs)	HMOX1 (W101fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2759906	NM_002133.3(HMOX1):c.304C>T (p.Gln102Ter)	HMOX1 (Q102*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2764976	NM_002133.3(HMOX1):c.309G>A (p.Glu103=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 15896	NM_002133.3(HMOX1):c.324_325del (p.Pro109fs)	HMOX1 (P109fs)	Microsatellite (frameshift variant)	Heme oxygenase 1 deficiency	GPathogenic
Select item 1501865	NM_002133.3(HMOX1):c.322A>G (p.Thr108Ala)	HMOX1 (T108A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2831853	NM_002133.3(HMOX1):c.324A>T (p.Thr108=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2390978	NM_002133.3(HMOX1):c.329C>T (p.Ala110Val)	HMOX1 (A110V)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 498177	NM_002133.3(HMOX1):c.330C>T (p.Ala110=)	HMOX1	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 1050403	NM_002133.3(HMOX1):c.334_345del (p.Gln112_Val115del)	HMOX1	Deletion (inframe_deletion)	not provided	GUncertain significance
Select item 1433185	NM_002133.3(HMOX1):c.337C>T (p.Arg113Cys)	HMOX1 (R113C)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1427669	NM_002133.3(HMOX1):c.338G>A (p.Arg113His)	HMOX1 (R113H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2826257	NM_002133.3(HMOX1):c.342T>C (p.Tyr114=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2697871	NM_002133.3(HMOX1):c.345G>A (p.Val115=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1974613	NM_002133.3(HMOX1):c.348G>A (p.Lys116=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2419704	NM_002133.3(HMOX1):c.349C>T (p.Arg117Trp)	HMOX1 (R117W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1400017	NM_002133.3(HMOX1):c.350G>A (p.Arg117Gln)	HMOX1 (R117Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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