ClinVar for Gene (Select 374291) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3188411	NM_024407.5(NDUFS7):c.59G>T (p.Ser20Ile)	NDUFS7 (S20I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3188409	NM_024407.5(NDUFS7):c.562G>A (p.Glu188Lys)	NDUFS7 (E188K)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3188401	NM_024407.5(NDUFS7):c.499G>C (p.Val167Leu)	NDUFS7 (V167L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3188380	NM_024407.5(NDUFS7):c.167C>T (p.Pro56Leu)	NDUFS7 (P56L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3062388	GRCh37/hg19 19p13.3(chr19:1365449-1390191)x1	NDUFS7, PWWP3A	Copy number loss	not specified	GUncertain significance
Select item 3052094	NM_024407.5(NDUFS7):c.*5G>A	NDUFS7	Single nucleotide variant (3 prime UTR variant)	NDUFS7-related condition	GLikely benign
Select item 3051826	NM_024407.5(NDUFS7):c.468A>C (p.Gly156=)	NDUFS7	Single nucleotide variant (synonymous variant)	NDUFS7-related condition	GLikely benign
Select item 3051720	NM_024407.5(NDUFS7):c.498G>C (p.Val166=)	NDUFS7	Single nucleotide variant (synonymous variant)	NDUFS7-related condition	GLikely benign
Select item 3051133	NM_024407.5(NDUFS7):c.513C>T (p.Asp171=)	NDUFS7	Single nucleotide variant (synonymous variant)	NDUFS7-related condition	GLikely benign
Select item 3050981	NM_024407.5(NDUFS7):c.502A>C (p.Arg168=)	NDUFS7	Single nucleotide variant (synonymous variant)	NDUFS7-related condition	GLikely benign
Select item 3023718	NM_024407.5(NDUFS7):c.53+14T>C	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3022568	NM_024407.5(NDUFS7):c.343_352dup (p.Asp118fs)	NDUFS7 (D118fs)	Duplication (frameshift variant)	not provided	GPathogenic
Select item 3022444	NM_024407.5(NDUFS7):c.455+20del	NDUFS7	Deletion (intron variant)	not provided	GLikely benign
Select item 3022249	NM_024407.5(NDUFS7):c.229-12C>T	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3021728	NM_024407.5(NDUFS7):c.544+19C>T	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3021265	NM_024407.5(NDUFS7):c.229-4G>A	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3015079	NM_024407.5(NDUFS7):c.495G>A (p.Ser165=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3010728	NM_024407.5(NDUFS7):c.351C>T (p.Ser117=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3010068	NM_024407.5(NDUFS7):c.39G>T (p.Arg13=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3008661	NM_024407.5(NDUFS7):c.229-17G>C	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3008583	NM_024407.5(NDUFS7):c.471A>C (p.Gly157=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3006783	NM_024407.5(NDUFS7):c.456-19C>G	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3005491	NM_024407.5(NDUFS7):c.229-17G>A	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3004510	NM_024407.5(NDUFS7):c.303C>T (p.Tyr101=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3000223	NM_024407.5(NDUFS7):c.409-11C>T	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2999570	NM_024407.5(NDUFS7):c.474C>T (p.Gly158=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2998869	NM_024407.5(NDUFS7):c.408+8T>G	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2998548	NM_024407.5(NDUFS7):c.37C>A (p.Arg13=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2996315	NM_024407.5(NDUFS7):c.447C>T (p.Ser149=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2995544	NM_024407.5(NDUFS7):c.627C>A (p.Ile209=)	NDUFS7	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2989590	NM_024407.5(NDUFS7):c.16+25_16+40dup	NDUFS7	Duplication (intron variant)	not provided	GLikely benign
Select item 2987431	NM_024407.5(NDUFS7):c.229-5C>T	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2985453	NM_024407.5(NDUFS7):c.123-18C>T	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2984045	NM_024407.5(NDUFS7):c.585G>C (p.Leu195=)	NDUFS7	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2981406	NM_024407.5(NDUFS7):c.122+12C>T	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2980990	NM_024407.5(NDUFS7):c.544+14C>T	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2980523	NM_024407.5(NDUFS7):c.189G>A (p.Val63=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2980487	NM_024407.5(NDUFS7):c.198G>A (p.Lys66=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2980130	NM_024407.5(NDUFS7):c.122+11C>A	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2978937	NM_024407.5(NDUFS7):c.409-20G>A	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2977334	NM_024407.5(NDUFS7):c.408+19G>A	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2977251	NM_024407.5(NDUFS7):c.456-10del	NDUFS7	Deletion (intron variant)	not provided	GLikely benign
Select item 2977205	NM_024407.5(NDUFS7):c.408+16G>A	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2975934	NM_024407.5(NDUFS7):c.456-19C>T	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2974700	NM_024407.5(NDUFS7):c.438C>T (p.Tyr146=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2974311	NM_024407.5(NDUFS7):c.16+16G>A	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2973976	NM_024407.5(NDUFS7):c.195C>T (p.Ala65=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2973032	NM_024407.5(NDUFS7):c.180C>G (p.Gly60=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2970772	NM_024407.5(NDUFS7):c.267C>T (p.Cys89=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2970673	NM_024407.5(NDUFS7):c.123-13G>A	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2969460	NM_024407.5(NDUFS7):c.621G>A (p.Leu207=)	NDUFS7	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2969413	NM_024407.5(NDUFS7):c.53+10T>G	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2966500	NM_024407.5(NDUFS7):c.465C>T (p.Asn155=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2966106	NM_024407.5(NDUFS7):c.123-13G>C	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2963740	NM_024407.5(NDUFS7):c.333C>T (p.Arg111=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2962726	NM_024407.5(NDUFS7):c.123-15G>C	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2962665	NM_024407.5(NDUFS7):c.123-20C>A	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2961640	NM_024407.5(NDUFS7):c.16+14C>T	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2961368	NM_024407.5(NDUFS7):c.409-11CT[4]	NDUFS7	Microsatellite (intron variant)	not provided	GLikely benign
Select item 2959198	NM_024407.5(NDUFS7):c.60C>T (p.Ser20=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2957829	NM_024407.5(NDUFS7):c.339_348del (p.Arg115fs)	NDUFS7 (R115fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2957444	NM_024407.5(NDUFS7):c.229-18C>T	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2906099	NM_024407.5(NDUFS7):c.342G>A (p.Pro114=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2904445	NM_024407.5(NDUFS7):c.429G>A (p.Glu143=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2899937	NM_024407.5(NDUFS7):c.99C>T (p.Ser33=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2899853	NM_024407.5(NDUFS7):c.16+7G>A	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2898982	NM_024407.5(NDUFS7):c.30C>T (p.Arg10=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2895348	NM_024407.5(NDUFS7):c.545-8C>T	NDUFS7	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2891176	NM_024407.5(NDUFS7):c.576C>T (p.Tyr192=)	NDUFS7	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2885353	NM_024407.5(NDUFS7):c.408+10G>C	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2881188	NM_024407.5(NDUFS7):c.456-17C>G	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2881161	NM_024407.5(NDUFS7):c.455+19del	NDUFS7	Deletion (intron variant)	not provided	GBenign
Select item 2878243	NM_024407.5(NDUFS7):c.122+17G>C	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2877088	NM_024407.5(NDUFS7):c.53+19A>G	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2876715	NM_024407.5(NDUFS7):c.249C>T (p.Thr83=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2872896	NM_024407.5(NDUFS7):c.409-14C>T	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2872884	NM_024407.5(NDUFS7):c.16+25_16+40del	NDUFS7	Deletion (intron variant)	not provided	GLikely benign
Select item 2872017	NM_024407.5(NDUFS7):c.51G>T (p.Leu17=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2871423	NM_024407.5(NDUFS7):c.6G>A (p.Ala2=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2869167	NM_024407.5(NDUFS7):c.408+18C>A	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2864077	NM_024407.5(NDUFS7):c.408+9C>G	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2861693	NM_024407.5(NDUFS7):c.252C>T (p.Phe84=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2857867	NM_024407.5(NDUFS7):c.123-1G>C	NDUFS7	Single nucleotide variant (splice acceptor variant)	not provided	GLikely pathogenic
Select item 2855941	NM_024407.5(NDUFS7):c.408+12C>T	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2853153	NM_024407.5(NDUFS7):c.456-13G>A	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2850961	NM_024407.5(NDUFS7):c.57C>T (p.Ser19=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2849905	NM_024407.5(NDUFS7):c.516C>A (p.Arg172=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2846960	NM_024407.5(NDUFS7):c.456-16G>T	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2846904	NM_024407.5(NDUFS7):c.420G>A (p.Gln140=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2846256	NM_024407.5(NDUFS7):c.545-4G>T	NDUFS7	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2845160	NM_024407.5(NDUFS7):c.409-13G>T	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2840349	NM_024407.5(NDUFS7):c.17-1G>T	NDUFS7	Single nucleotide variant (splice acceptor variant)	not provided	GLikely pathogenic
Select item 2839474	NM_024407.5(NDUFS7):c.16+12A>G	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2839406	NM_024407.5(NDUFS7):c.525C>G (p.Pro175=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2838236	NM_024407.5(NDUFS7):c.17-12T>C	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2836486	NM_024407.5(NDUFS7):c.399G>T (p.Ala133=)	NDUFS7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2829143	NM_024407.5(NDUFS7):c.267C>A (p.Cys89Ter)	NDUFS7 (C89*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2824352	NM_024407.5(NDUFS7):c.639G>A (p.Arg213=)	NDUFS7	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2819120	NM_024407.5(NDUFS7):c.455+2T>C	NDUFS7	Single nucleotide variant (splice donor variant)	not provided	GLikely pathogenic
Select item 2815280	NM_024407.5(NDUFS7):c.122+17G>A	NDUFS7	Single nucleotide variant (intron variant)	not provided	GLikely benign

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