Nup62cl Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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18 records found for search term Nup62cl

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156040374	CV2387594	single nucleotide variant	NM_017681.3(NUP62CL):c.19T>C (p.Ser7Pro)	not specified [RCV004234145]	uncertain significance	X	107175128	107175128	Human		name
401889058	CV2761714	single nucleotide variant	NM_017681.3(NUP62CL):c.26C>A (p.Ser9Tyr)	not specified [RCV004337328]	uncertain significance	X	107175121	107175121	Human		name
401921286	CV2826734	single nucleotide variant	NM_017681.3(NUP62CL):c.219A>G (p.Thr73=)	not provided [RCV003432321]	likely benign	X	107154222	107154222	Human		name
156165210	CV2270329	single nucleotide variant	NM_017681.3(NUP62CL):c.70A>G (p.Thr24Ala)	not specified [RCV004135534]	uncertain significance	X	107167773	107167773	Human		name
156173494	CV2194358	single nucleotide variant	NM_017681.3(NUP62CL):c.250T>C (p.Trp84Arg)	not specified [RCV004079465]	uncertain significance	X	107154191	107154191	Human		name
405680641	CV3352479	single nucleotide variant	NM_017681.3(NUP62CL):c.103A>G (p.Thr35Ala)	not specified [RCV004488612]	uncertain significance	X	107167740	107167740	Human		name
405680649	CV3352480	single nucleotide variant	NM_017681.3(NUP62CL):c.158G>A (p.Gly53Glu)	not specified [RCV004488613]	uncertain significance	X	107167685	107167685	Human		name
407522415	CV3458997	single nucleotide variant	NM_017681.3(NUP62CL):c.104C>T (p.Thr35Ile)	not specified [RCV004652757]	uncertain significance	X	107167739	107167739	Human		name
407522297	CV3458998	single nucleotide variant	NM_017681.3(NUP62CL):c.232G>A (p.Glu78Lys)	not specified [RCV004652758]	uncertain significance	X	107154209	107154209	Human		name
597664675	CV3570085	single nucleotide variant	NM_017681.3(NUP62CL):c.221A>G (p.Tyr74Cys)	not specified [RCV004835486]	uncertain significance	X	107154220	107154220	Human		name
597664683	CV3570086	single nucleotide variant	NM_017681.3(NUP62CL):c.226C>T (p.His76Tyr)	not specified [RCV004835487]	uncertain significance	X	107154215	107154215	Human		name
598235451	CV4004845	single nucleotide variant	NM_017681.3(NUP62CL):c.211G>A (p.Val71Met)	not specified [RCV005382010]	uncertain significance	X	107154230	107154230	Human		name
156386203	CV2228143	single nucleotide variant	NM_017681.3(NUP62CL):c.317A>G (p.Asp106Gly)	not specified [RCV004096359]	uncertain significance	X	107154124	107154124	Human		name
156107803	CV2254340	single nucleotide variant	NM_017681.3(NUP62CL):c.485G>C (p.Ser162Thr)	not specified [RCV004123738]	uncertain significance	X	107153217	107153217	Human		name
156148777	CV2292807	single nucleotide variant	NM_017681.3(NUP62CL):c.475C>T (p.Arg159Cys)	not specified [RCV004154463]	uncertain significance	X	107153227	107153227	Human		name
156231229	CV2348747	single nucleotide variant	NM_017681.3(NUP62CL):c.473C>T (p.Thr158Met)	not specified [RCV004201154]	likely benign	X	107153229	107153229	Human		name
405680654	CV3352481	single nucleotide variant	NM_017681.3(NUP62CL):c.350G>A (p.Arg117His)	not specified [RCV004488614]	uncertain significance	X	107153499	107153499	Human		name
597664690	CV3570088	single nucleotide variant	NM_017681.3(NUP62CL):c.521A>G (p.His174Arg)	not specified [RCV004835488]	likely benign	X	107153181	107153181	Human		name