ClinVar for Gene (Select 3033) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3361159	NM_005327.7(HADH):c.268G>A (p.Asp90Asn)	HADH (D90N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3349755	NM_005327.7(HADH):c.710-791G>C	HADH	Single nucleotide variant (intron variant)	HADH-related disorder	GLikely benign
Select item 3340505	NM_005327.7(HADH):c.132G>A (p.Gln44=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase +1 more	GUncertain significance
Select item 3246656	NC_000004.11:g.(?_108911089)_(108911240_?)del	HADH	Deletion	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GPathogenic
Select item 3246655	NC_000004.11:g.(?_108911089)_(108955513_?)del	HADH	Deletion	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GPathogenic
Select item 3241724	NM_005327.7(HADH):c.271G>T (p.Glu91Ter)	HADH (E91* +1 more)	Single nucleotide variant (nonsense)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely pathogenic
Select item 3241723	NM_005327.7(HADH):c.710-1G>A	HADH	Single nucleotide variant (splice acceptor variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely pathogenic
Select item 3104132	NM_005327.7(HADH):c.596A>G (p.Asp199Gly)	HADH (D203G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3104131	NM_005327.7(HADH):c.491A>T (p.Asp164Val)	HADH (D168V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3104130	NM_005327.7(HADH):c.421C>T (p.His141Tyr)	HADH (H145Y +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3062767	GRCh37/hg19 4q24-35.2(chr4:101203509-190957473)x3	AADAT, ABCE1 +286 more	Copy number gain	not specified	GPathogenic
Select item 3038120	NM_005327.7(HADH):c.710-857C>T	HADH	Single nucleotide variant (intron variant)	HADH-related disorder	GLikely benign
Select item 3036274	NM_005327.7(HADH):c.-5AC[1]	HADH	Microsatellite (5 prime UTR variant)	HADH-related disorder	GLikely benign
Select item 3034377	NM_005327.7(HADH):c.709+35_709+36insG	HADH	Insertion (intron variant)	HADH-related disorder	GLikely benign
Select item 3034297	NM_005327.7(HADH):c.709+32A>G	HADH	Single nucleotide variant (intron variant)	HADH-related disorder	GLikely benign
Select item 3034225	NM_005327.7(HADH):c.709+33C>T	HADH	Single nucleotide variant (intron variant)	HADH-related disorder	GLikely benign
Select item 3033981	NM_005327.7(HADH):c.709+37A>T	HADH	Single nucleotide variant (intron variant)	HADH-related disorder	GLikely benign
Select item 3032721	NM_005327.7(HADH):c.105C>T (p.Gly35=)	HADH	Single nucleotide variant (synonymous variant)	HADH-related disorder	GLikely benign
Select item 3029815	NM_005327.7(HADH):c.537A>G (p.Lys179=)	HADH	Single nucleotide variant (synonymous variant)	HADH-related disorder	GLikely benign
Select item 3029497	NM_005327.7(HADH):c.15C>T (p.Thr5=)	HADH	Single nucleotide variant (synonymous variant)	HADH-related disorder	GLikely benign
Select item 3024631	GRCh37/hg19 4p12-q35.2(chr4:45455621-191003541)x3	HPGDS, SCRG1 +537 more	Copy number gain	not provided	GPathogenic
Select item 3017483	NM_005327.7(HADH):c.710-19G>A	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 3015814	NM_005327.7(HADH):c.351G>A (p.Val117=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 3014410	NM_005327.7(HADH):c.39C>T (p.Ser13=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 3012788	NM_005327.7(HADH):c.498C>T (p.Phe166=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 3012445	NM_005327.7(HADH):c.827-20C>T	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 3008943	NM_005327.7(HADH):c.249A>G (p.Ala83=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 3007880	NM_005327.7(HADH):c.567C>T (p.Thr189=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 3006363	NM_005327.7(HADH):c.327T>C (p.Val109=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 3004690	NM_005327.7(HADH):c.921A>T (p.Gly307=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 3002807	NM_005327.7(HADH):c.306C>G (p.Thr102=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2999976	NM_005327.7(HADH):c.774A>G (p.Pro258=)	HADH	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2997131	NM_005327.7(HADH):c.156A>G (p.Thr52=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2994373	NM_005327.7(HADH):c.262-5A>C	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2977206	NM_005327.7(HADH):c.162G>A (p.Val54=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2975726	NM_005327.7(HADH):c.261+10T>C	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2964859	NM_005327.7(HADH):c.261+16C>A	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2960014	NM_005327.7(HADH):c.827-18C>T	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2916167	NM_005327.7(HADH):c.312G>A (p.Thr104=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2915473	NM_005327.7(HADH):c.828G>A (p.Gly276=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2909979	NM_005327.7(HADH):c.262-8T>C	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2908014	NM_005327.7(HADH):c.636+7G>C	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2904210	NM_005327.7(HADH):c.262-6C>T	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2891714	NM_005327.7(HADH):c.132+19A>G	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2890622	NM_005327.7(HADH):c.261+18A>T	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2886955	NM_005327.7(HADH):c.419+14G>A	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2883026	NM_005327.7(HADH):c.600T>C (p.Phe200=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2882402	NM_005327.7(HADH):c.615A>G (p.Gly205=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2882063	NM_005327.7(HADH):c.525G>A (p.Val175=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2877074	NM_005327.7(HADH):c.826+13del	HADH	Deletion (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2875489	NM_005327.7(HADH):c.709+17G>A	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2874401	NM_005327.7(HADH):c.426A>G (p.Thr142=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2874131	NM_005327.7(HADH):c.261+2T>A	HADH	Single nucleotide variant (splice donor variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely pathogenic
Select item 2869871	NM_005327.7(HADH):c.637-18T>C	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2869097	NM_005327.7(HADH):c.637-7A>C	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2868716	NM_005327.7(HADH):c.93G>A (p.Thr31=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2866201	NM_005327.7(HADH):c.261+15T>A	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2862884	NM_005327.7(HADH):c.663C>T (p.Arg221=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2862079	NM_005327.7(HADH):c.48C>T (p.Ser16=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2853170	NM_005327.7(HADH):c.420-19C>T	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2846842	NM_005327.7(HADH):c.381A>G (p.Lys127=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2844359	NM_005327.7(HADH):c.547-19C>A	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2841833	NM_005327.7(HADH):c.54C>A (p.Ala18=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2841632	NM_005327.7(HADH):c.710-14_710-11dup	HADH	Duplication (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2841592	NM_005327.7(HADH):c.489A>G (p.Gln163=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2841482	NM_005327.7(HADH):c.612A>G (p.Leu204=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2836479	NM_005327.7(HADH):c.64del (p.Ala22fs)	HADH (A22fs)	Deletion (frameshift variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GPathogenic
Select item 2836291	NM_005327.7(HADH):c.771C>T (p.Gly257=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2832318	NM_005327.7(HADH):c.909C>T (p.Gly303=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2828916	NM_005327.7(HADH):c.450C>T (p.Ser150=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2826330	NM_005327.7(HADH):c.369del (p.Asn123_Leu124insTer)	HADH	Deletion (frameshift variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GPathogenic
Select item 2820792	NM_005327.7(HADH):c.420-10C>T	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2809363	NM_005327.7(HADH):c.664_668del (p.Leu222fs)	HADH (L222fs +1 more)	Deletion (frameshift variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GPathogenic
Select item 2806151	NM_005327.7(HADH):c.546+13C>T	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2805111	NM_005327.7(HADH):c.117C>G (p.Gly39=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2802479	NM_005327.7(HADH):c.873A>G (p.Pro291=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2799758	NM_005327.7(HADH):c.87C>T (p.His29=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2799307	NM_005327.7(HADH):c.180G>A (p.Glu60=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2797432	NM_005327.7(HADH):c.366G>A (p.Glu122=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2796951	NM_005327.7(HADH):c.493C>T (p.Arg165Ter)	HADH (R165* +1 more)	Single nucleotide variant (nonsense)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GPathogenic
Select item 2794776	NM_005327.7(HADH):c.141A>G (p.Ala47=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2793908	NM_005327.7(HADH):c.261+8C>G	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2785744	NM_005327.7(HADH):c.765C>G (p.Pro255=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2781679	NM_005327.7(HADH):c.261+7T>A	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2780531	NM_005327.7(HADH):c.261+19T>A	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2778619	NM_005327.7(HADH):c.710-11T>A	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2777116	NM_005327.7(HADH):c.637-10C>T	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2770114	NM_005327.7(HADH):c.419+18A>G	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2770111	NM_005327.7(HADH):c.419+16A>T	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2769989	NM_005327.7(HADH):c.126T>C (p.Ile42=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2768349	NM_005327.7(HADH):c.132+16T>A	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2767809	NM_005327.7(HADH):c.546+15G>T	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2767734	NM_005327.7(HADH):c.261+20G>A	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2764177	NM_005327.7(HADH):c.636+18T>C	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2763835	NM_005327.7(HADH):c.315T>C (p.Asp105=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2761586	NM_005327.7(HADH):c.756C>G (p.Ala252=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2758232	NM_005327.7(HADH):c.304_307dup (p.Ser103fs)	HADH (S107fs +1 more)	Duplication (frameshift variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GPathogenic
Select item 2754624	NM_005327.7(HADH):c.636+16G>T	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2749753	NM_005327.7(HADH):c.261+16C>G	HADH	Single nucleotide variant (intron variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign
Select item 2746550	NM_005327.7(HADH):c.897G>A (p.Glu299=)	HADH	Single nucleotide variant (synonymous variant)	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	GLikely benign

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