ClinVar for Gene (Select 3162) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3366998	NM_002133.3(HMOX1):c.73C>T (p.His25Tyr)	HMOX1 (H25Y)	Single nucleotide variant (missense variant)	Heme oxygenase 1 deficiency	GUncertain significance
Select item 3284520	NM_002133.3(HMOX1):c.305A>G (p.Gln102Arg)	HMOX1 (Q102R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3248114	NC_000022.10:g.(?_35776672)_(35799555_?)dup	HMOX1, MCM5	Duplication	not provided	GUncertain significance
Select item 3106332	NM_002133.3(HMOX1):c.842T>C (p.Val281Ala)	HMOX1 (V281A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3019075	NM_002133.3(HMOX1):c.300C>A (p.Arg100=)	HMOX1	Single nucleotide variant (synonymous 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 3007963	NM_002133.3(HMOX1):c.228del (p.Val77fs)	HMOX1 (V77fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 3005762	NM_002133.3(HMOX1):c.145-4del	HMOX1	Deletion (intron variant)	not provided	GLikely benign
Select item 3004273	NM_002133.3(HMOX1):c.213C>T (p.Ser71=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3003636	NM_002133.3(HMOX1):c.813C>G (p.Val271=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3000980	NM_002133.3(HMOX1):c.636+10G>A	HMOX1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3000857	NM_002133.3(HMOX1):c.612G>C (p.Lys204Asn)	HMOX1 (K204N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3000769	NM_002133.3(HMOX1):c.150G>C (p.Val50=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2999690	NM_002133.3(HMOX1):c.736+12C>G	HMOX1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2998155	NM_002133.3(HMOX1):c.678G>A (p.Lys226=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2998017	NM_002133.3(HMOX1):c.23+12G>A	HMOX1, LOC130067299	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2991040	NM_002133.3(HMOX1):c.737-12T>A	HMOX1	Single nucleotide variant (intron 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 2987596	NM_002133.3(HMOX1):c.483C>T (p.Gly161=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2986515	NM_002133.3(HMOX1):c.636+19_636+28del	HMOX1	Deletion (intron variant)	not provided	GLikely benign
Select item 2985933	NM_002133.3(HMOX1):c.237C>T (p.Phe79=)	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 2981777	NM_002133.3(HMOX1):c.690C>A (p.Pro230=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2979226	NM_002133.3(HMOX1):c.145-18T>G	HMOX1	Single nucleotide variant (intron 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 2978517	NM_002133.3(HMOX1):c.23+17G>C	HMOX1, LOC130067299	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 2971203	NM_002133.3(HMOX1):c.99C>T (p.Phe33=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2957947	NM_002133.3(HMOX1):c.207G>A (p.Lys69=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2957525	NM_002133.3(HMOX1):c.737-16C>G	HMOX1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2956545	NM_002133.3(HMOX1):c.636+17C>T	HMOX1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2908426	NM_002133.3(HMOX1):c.18C>T (p.Pro6=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2900750	NM_002133.3(HMOX1):c.720C>T (p.Ala240=)	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 2888491	NM_002133.3(HMOX1):c.579C>G (p.Pro193=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2886483	NM_002133.3(HMOX1):c.585C>T (p.Val195=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2877655	NM_002133.3(HMOX1):c.777C>T (p.Leu259=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2869294	NM_002133.3(HMOX1):c.604G>T (p.Glu202Ter)	HMOX1 (E202*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2868250	NM_002133.3(HMOX1):c.715C>A (p.Arg239=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2867354	NM_002133.3(HMOX1):c.636+7G>T	HMOX1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2864581	NM_002133.3(HMOX1):c.737-4T>C	HMOX1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2863920	NM_002133.3(HMOX1):c.636+13C>T	HMOX1	Single nucleotide variant (intron 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 2861185	NM_002133.3(HMOX1):c.639C>T (p.Leu213=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2857270	NM_002133.3(HMOX1):c.737-13T>A	HMOX1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2851707	NM_002133.3(HMOX1):c.417T>C (p.Gly139=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
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 2843012	NM_002133.3(HMOX1):c.636+16C>T	HMOX1	Single nucleotide variant (intron 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 2841479	NM_002133.3(HMOX1):c.303_328del (p.Trp101fs)	HMOX1 (W101fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2840397	NM_002133.3(HMOX1):c.23+1G>T	HMOX1, LOC130067299	Single nucleotide variant (splice donor variant)	not provided	GLikely pathogenic
Select item 2837038	NM_002133.3(HMOX1):c.459del (p.Ala154fs)	HMOX1 (A154fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2836347	NM_002133.3(HMOX1):c.285C>T (p.Phe95=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2835836	NM_002133.3(HMOX1):c.732G>A (p.Val244=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2834210	NM_002133.3(HMOX1):c.705G>C (p.Gly235=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2831853	NM_002133.3(HMOX1):c.324A>T (p.Thr108=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2830455	NM_002133.3(HMOX1):c.382C>T (p.Leu128=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2829805	NM_002133.3(HMOX1):c.747C>G (p.Pro249=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2829745	NM_002133.3(HMOX1):c.405C>T (p.Thr135=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2827675	NM_002133.3(HMOX1):c.156C>G (p.Ala52=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2826257	NM_002133.3(HMOX1):c.342T>C (p.Tyr114=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2824386	NM_002133.3(HMOX1):c.219C>T (p.Val73=)	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 2821367	NM_002133.3(HMOX1):c.737-13T>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 2817414	NM_002133.3(HMOX1):c.57G>A (p.Glu19=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2815052	NM_002133.3(HMOX1):c.135_139del (p.Gly46fs)	HMOX1 (G46fs)	Deletion (frameshift variant)	not provided	GPathogenic
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 2812121	NM_002133.3(HMOX1):c.561C>T (p.Asn187=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2803892	NM_002133.3(HMOX1):c.567G>C (p.Leu189=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2801727	NM_002133.3(HMOX1):c.363G>T (p.Val121=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2799543	NM_002133.3(HMOX1):c.294G>A (p.Gly98=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2797656	NM_002133.3(HMOX1):c.737-9C>G	HMOX1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2796654	NM_002133.3(HMOX1):c.393C>G (p.Ala131=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2795711	NM_002133.3(HMOX1):c.737-15C>T	HMOX1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2795325	NM_002133.3(HMOX1):c.750G>A (p.Val250=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2789178	NM_002133.3(HMOX1):c.384G>A (p.Leu128=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2788961	NM_002133.3(HMOX1):c.469C>T (p.Leu157=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2788489	NM_002133.3(HMOX1):c.117G>A (p.Lys39=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2788372	NM_002133.3(HMOX1):c.615T>C (p.Thr205=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2786250	NM_002133.3(HMOX1):c.23+11G>A	HMOX1, LOC130067299	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2786239	NM_002133.3(HMOX1):c.23+8_23+23del	HMOX1, LOC130067299	Deletion (intron variant)	not provided	GLikely benign
Select item 2785180	NM_002133.3(HMOX1):c.711C>G (p.Arg237=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2784596	NM_002133.3(HMOX1):c.372A>G (p.Thr124=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2784133	NM_002133.3(HMOX1):c.652C>T (p.Gln218Ter)	HMOX1 (Q218*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2773053	NM_002133.3(HMOX1):c.420C>T (p.Asp140=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2771737	NM_002133.3(HMOX1):c.247C>T (p.Leu83=)	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 2764976	NM_002133.3(HMOX1):c.309G>A (p.Glu103=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2764359	NM_002133.3(HMOX1):c.144+1G>A	HMOX1	Single nucleotide variant (splice donor variant)	not provided	GLikely pathogenic
Select item 2763622	NM_002133.3(HMOX1):c.666C>T (p.Thr222=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2763521	NM_002133.3(HMOX1):c.447G>A (p.Lys149=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2762783	NM_002133.3(HMOX1):c.726C>T (p.Asn242=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2761054	NM_002133.3(HMOX1):c.744C>A (p.Ala248=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2760022	NM_002133.3(HMOX1):c.444A>G (p.Lys148=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2759906	NM_002133.3(HMOX1):c.304C>T (p.Gln102Ter)	HMOX1 (Q102*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2758852	NM_002133.3(HMOX1):c.468C>T (p.Asp156=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2757129	NM_002133.3(HMOX1):c.414G>A (p.Leu138=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2755568	NM_002133.3(HMOX1):c.412C>T (p.Leu138=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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