Plscr5 Variant Search Result - Rat Genome Database

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23 records found for search term Plscr5

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156385492	CV2227940	single nucleotide variant	NM_001085420.2(PLSCR5):c.16G>T (p.Ala6Ser)	not specified [RCV004096195]	uncertain significance	3	146600461	146600461	Human		name
407471369	CV3467483	single nucleotide variant	NM_001085420.2(PLSCR5):c.14A>T (p.Asp5Val)	not specified [RCV004662262]	uncertain significance	3	146600463	146600463	Human		name
405793749	CV3365931	single nucleotide variant	NM_001085420.2(PLSCR5):c.53C>T (p.Pro18Leu)	not specified [RCV004506808]	uncertain significance	3	146600424	146600424	Human		name
598176042	CV4007064	single nucleotide variant	NM_001085420.2(PLSCR5):c.65A>G (p.Asp22Gly)	not specified [RCV005393578]	uncertain significance	3	146600412	146600412	Human		name
155984195	CV2273159	single nucleotide variant	NM_001085420.2(PLSCR5):c.271A>C (p.Lys91Gln)	not specified [RCV004137793]	uncertain significance	3	146594102	146594102	Human		name
156240212	CV2236021	single nucleotide variant	NM_001085420.2(PLSCR5):c.560T>G (p.Leu187Trp)	not specified [RCV004113887]	uncertain significance	3	146591775	146591775	Human		name
156162945	CV2246575	single nucleotide variant	NM_001085420.2(PLSCR5):c.551A>G (p.Glu184Gly)	not specified [RCV004110322]	uncertain significance	3	146591784	146591784	Human		name
156070570	CV2267172	single nucleotide variant	NM_001085420.2(PLSCR5):c.316A>T (p.Ile106Phe)	not specified [RCV004133860]	uncertain significance	3	146594057	146594057	Human		name
155905136	CV2298930	single nucleotide variant	NM_001085420.2(PLSCR5):c.733G>A (p.Asp245Asn)	not specified [RCV004156461]	uncertain significance	3	146589697	146589697	Human		name
155941614	CV2300885	single nucleotide variant	NM_001085420.2(PLSCR5):c.737T>A (p.Val246Glu)	not specified [RCV004158087]	uncertain significance	3	146589693	146589693	Human		name
156327142	CV2332063	single nucleotide variant	NM_001085420.2(PLSCR5):c.757A>G (p.Ile253Val)	not specified [RCV004189113]	uncertain significance	3	146589673	146589673	Human		name
329353595	CV2469337	single nucleotide variant	NM_001085420.2(PLSCR5):c.328C>T (p.Arg110Cys)	not specified [RCV004280668]	uncertain significance	3	146594045	146594045	Human		name
401730646	CV2689773	single nucleotide variant	NM_001085420.2(PLSCR5):c.631G>C (p.Glu211Gln)	not specified [RCV004297683]	uncertain significance	3	146589799	146589799	Human		name
401769631	CV2731481	single nucleotide variant	NM_001085420.2(PLSCR5):c.329G>T (p.Arg110Leu)	not specified [RCV004330835]	uncertain significance	3	146594044	146594044	Human		name
401857892	CV2774034	single nucleotide variant	NM_001085420.2(PLSCR5):c.583A>C (p.Thr195Pro)	not specified [RCV004345643]	uncertain significance	3	146591752	146591752	Human		name
405793747	CV3365930	single nucleotide variant	NM_001085420.2(PLSCR5):c.329G>A (p.Arg110His)	not specified [RCV004506807]	uncertain significance	3	146594044	146594044	Human		name
405793752	CV3365932	single nucleotide variant	NM_001085420.2(PLSCR5):c.698C>T (p.Ala233Val)	not specified [RCV004506809]	uncertain significance	3	146589732	146589732	Human		name
407471365	CV3467482	single nucleotide variant	NM_001085420.2(PLSCR5):c.761G>A (p.Gly254Asp)	not specified [RCV004662261]	uncertain significance	3	146589669	146589669	Human		name
407471373	CV3467484	single nucleotide variant	NM_001085420.2(PLSCR5):c.728A>G (p.Asp243Gly)	not specified [RCV004662263]	uncertain significance	3	146589702	146589702	Human		name
597768482	CV3573190	single nucleotide variant	NM_001085420.2(PLSCR5):c.716A>G (p.His239Arg)	not specified [RCV004850697]	uncertain significance	3	146589714	146589714	Human		name
597684169	CV3573191	single nucleotide variant	NM_001085420.2(PLSCR5):c.623C>A (p.Thr208Asn)	not specified [RCV004837709]	uncertain significance	3	146589807	146589807	Human		name
598176049	CV4007065	single nucleotide variant	NM_001085420.2(PLSCR5):c.397A>G (p.Thr133Ala)	not specified [RCV005393579]	uncertain significance	3	146593976	146593976	Human		name
598176056	CV4007066	single nucleotide variant	NM_001085420.2(PLSCR5):c.605T>C (p.Val202Ala)	not specified [RCV005393580]	uncertain significance	3	146591730	146591730	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
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