Commd7 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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27 records found for search term Commd7

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15202767	CV778580	single nucleotide variant	NM_053041.3(COMMD7):c.526+3G>A	not provided [RCV000958026]	benign	20	32704020	32704020	Human		name
405656999	CV3305470	single nucleotide variant	NM_053041.3(COMMD7):c.71A>G (p.Gln24Arg)	not specified [RCV004437751]	uncertain significance	20	32743321	32743321	Human		name
405657002	CV3305471	single nucleotide variant	NM_053041.3(COMMD7):c.95C>A (p.Ala32Asp)	not specified [RCV004437752]	uncertain significance	20	32728132	32728132	Human		name
597648345	CV3654090	single nucleotide variant	NM_053041.3(COMMD7):c.40G>T (p.Ala14Ser)	not specified [RCV004910236]	uncertain significance	20	32743352	32743352	Human		name
597648353	CV3654091	single nucleotide variant	NM_053041.3(COMMD7):c.52G>A (p.Asp18Asn)	not specified [RCV004910237]	uncertain significance	20	32743340	32743340	Human		name
597648360	CV3654092	single nucleotide variant	NM_053041.3(COMMD7):c.62A>C (p.Gln21Pro)	not specified [RCV004910238]	uncertain significance	20	32743330	32743330	Human		name
156263254	CV2282559	single nucleotide variant	NM_053041.3(COMMD7):c.121C>G (p.Leu41Val)	not specified [RCV004135130]	uncertain significance	20	32728106	32728106	Human		name
156134508	CV2362061	single nucleotide variant	NM_053041.3(COMMD7):c.281C>T (p.Ala94Val)	not specified [RCV004209872]	uncertain significance	20	32706721	32706721	Human		name
329363584	CV2442323	single nucleotide variant	NM_053041.3(COMMD7):c.176C>T (p.Thr59Ile)	not specified [RCV004264796]	uncertain significance	20	32727958	32727958	Human		name
401735053	CV2699148	single nucleotide variant	NM_053041.3(COMMD7):c.196G>T (p.Gly66Cys)	not specified [RCV004303649]	uncertain significance	20	32727938	32727938	Human		name
401762096	CV2722638	single nucleotide variant	NM_053041.3(COMMD7):c.128A>G (p.Glu43Gly)	not specified [RCV004325092]	uncertain significance	20	32728099	32728099	Human		name
597648957	CV3654093	single nucleotide variant	NM_053041.3(COMMD7):c.139G>A (p.Val47Met)	not specified [RCV004910239]	uncertain significance	20	32727995	32727995	Human		name
156232116	CV2199714	single nucleotide variant	NM_053041.3(COMMD7):c.511G>A (p.Glu171Lys)	not specified [RCV004072444]	uncertain significance	20	32704038	32704038	Human		name
156337183	CV2267211	single nucleotide variant	NM_053041.3(COMMD7):c.319A>G (p.Thr107Ala)	not specified [RCV004133894]	uncertain significance	20	32706600	32706600	Human		name
156269195	CV2326357	single nucleotide variant	NM_053041.3(COMMD7):c.538C>T (p.Pro180Ser)	not specified [RCV004182939]	uncertain significance	20	32703447	32703447	Human		name
156156490	CV2359853	single nucleotide variant	NM_053041.3(COMMD7):c.500G>T (p.Gly167Val)	not specified [RCV004212706]	uncertain significance	20	32704049	32704049	Human		name
329395965	CV2463117	single nucleotide variant	NM_053041.3(COMMD7):c.503A>G (p.Asn168Ser)	not specified [RCV004274916]	uncertain significance	20	32704046	32704046	Human		name
401727143	CV2684487	single nucleotide variant	NM_053041.3(COMMD7):c.472T>G (p.Leu158Val)	not specified [RCV004291559]	uncertain significance	20	32704445	32704445	Human		name
401877855	CV2786826	single nucleotide variant	NM_053041.3(COMMD7):c.362C>T (p.Ala121Val)	not specified [RCV004365987]	uncertain significance	20	32704879	32704879	Human		name
405656996	CV3305469	single nucleotide variant	NM_053041.3(COMMD7):c.343C>A (p.Gln115Lys)	not specified [RCV004437750]	uncertain significance	20	32704898	32704898	Human		name
407452155	CV3423294	single nucleotide variant	NM_053041.3(COMMD7):c.365G>A (p.Arg122Gln)	not specified [RCV004608325]	likely benign	20	32704876	32704876	Human		name
407452158	CV3423295	single nucleotide variant	NM_053041.3(COMMD7):c.434C>T (p.Ser145Phe)	not specified [RCV004608326]	uncertain significance	20	32704483	32704483	Human		name
597648336	CV3654089	single nucleotide variant	NM_053041.3(COMMD7):c.566T>C (p.Met189Thr)	not specified [RCV004910235]	uncertain significance	20	32703419	32703419	Human		name
597648964	CV3654094	single nucleotide variant	NM_053041.3(COMMD7):c.350C>T (p.Ala117Val)	not specified [RCV004910240]	uncertain significance	20	32704891	32704891	Human		name
598233622	CV3948820	single nucleotide variant	NM_053041.3(COMMD7):c.490G>A (p.Val164Ile)	not specified [RCV005319958]	uncertain significance	20	32704059	32704059	Human		name
598233630	CV3948821	single nucleotide variant	NM_053041.3(COMMD7):c.445G>A (p.Glu149Lys)	not specified [RCV005319959]	uncertain significance	20	32704472	32704472	Human		name
598233639	CV3948822	single nucleotide variant	NM_053041.3(COMMD7):c.565A>G (p.Met189Val)	not specified [RCV005319960]	uncertain significance	20	32703420	32703420	Human		name

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