Sebox Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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17 records found for search term Sebox

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401753384	CV2674874	single nucleotide variant	NM_001080837.4(SEBOX):c.-26C>T	not specified [RCV004294143]	uncertain significance	17	28365177	28365177	Human		name
405703611	CV3310563	single nucleotide variant	NM_001080837.4(SEBOX):c.-11T>C	not specified [RCV004447451]	likely benign	17	28365162	28365162	Human		name
405703598	CV3310561	single nucleotide variant	NM_001080837.2(SEBOX):c.4G>A (p.Gly2Arg)	not specified [RCV004447449]	uncertain significance	17	28365227	28365227	Human		name
405703574	CV3310558	single nucleotide variant	NM_001080837.4(SEBOX):c.34G>A (p.Gly12Ser)	not specified [RCV004447446]	uncertain significance	17	28364953	28364953	Human		name
405703580	CV3310559	single nucleotide variant	NM_001080837.4(SEBOX):c.58C>T (p.Arg20Trp)	not specified [RCV004447447]	uncertain significance	17	28364929	28364929	Human		name
407476783	CV3476599	single nucleotide variant	NM_001080837.4(SEBOX):c.59G>A (p.Arg20Gln)	not specified [RCV004663564]	likely benign	17	28364928	28364928	Human		name
401747559	CV2696732	single nucleotide variant	NM_001080837.4(SEBOX):c.186G>C (p.Lys62Asn)	not specified [RCV004290706]	uncertain significance	17	28364801	28364801	Human		name
401777756	CV2704318	single nucleotide variant	NM_001080837.4(SEBOX):c.153C>G (p.His51Gln)	not specified [RCV004311301]	uncertain significance	17	28364834	28364834	Human		name
405703590	CV3310560	single nucleotide variant	NM_001080837.4(SEBOX):c.292G>A (p.Asp98Asn)	not specified [RCV004447448]	uncertain significance	17	28364549	28364549	Human		name
407491969	CV3476601	single nucleotide variant	NM_001080837.4(SEBOX):c.134A>G (p.Asn45Ser)	not specified [RCV004666991]	uncertain significance	17	28364853	28364853	Human		name
401894168	CV2770377	single nucleotide variant	NM_001080837.4(SEBOX):c.482C>G (p.Ser161Cys)	not specified [RCV004358026]	uncertain significance	17	28364359	28364359	Human		name
405703602	CV3310562	single nucleotide variant	NM_001080837.4(SEBOX):c.448T>C (p.Trp150Arg)	not specified [RCV004447450]	likely benign	17	28364393	28364393	Human		name
407491965	CV3476600	single nucleotide variant	NM_001080837.4(SEBOX):c.413G>A (p.Arg138Gln)	not specified [RCV004666990]	uncertain significance	17	28364428	28364428	Human		name
597714623	CV3605338	single nucleotide variant	NM_001080837.4(SEBOX):c.412C>T (p.Arg138Trp)	not specified [RCV004861383]	uncertain significance	17	28364429	28364429	Human		name
598209979	CV3907050	single nucleotide variant	NM_001080837.4(SEBOX):c.362G>A (p.Arg121His)	not specified [RCV005270601]	uncertain significance	17	28364479	28364479	Human		name
598209986	CV3907051	single nucleotide variant	NM_001080837.4(SEBOX):c.430G>T (p.Ala144Ser)	not specified [RCV005270602]	uncertain significance	17	28364411	28364411	Human		name
598209993	CV3907052	single nucleotide variant	NM_001080837.4(SEBOX):c.554T>A (p.Val185Asp)	not specified [RCV005270603]	uncertain significance	17	28364287	28364287	Human		name