Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Behavioral & Substance Use Disorder Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Advanced Search (OLGA)
Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)

35 records found for search term Ppil6
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401877136CV2790061single nucleotide variantNM_173672.5(PPIL6):c.689-2876A>Tnot specified [RCV004364011]uncertain significance6109403046109403046Humanname
405794471CV3366369single nucleotide variantNM_173672.5(PPIL6):c.689-2888G>Cnot specified [RCV004507071]uncertain significance6109403058109403058Humanname
407482819CV3471440single nucleotide variantNM_173672.5(PPIL6):c.689-2915A>Cnot specified [RCV004664838]uncertain significance6109403085109403085Humanname
156307243CV2335410single nucleotide variantNM_173672.5(PPIL6):c.11C>T (p.Pro4Leu)not specified [RCV004186964]uncertain significance6109440580109440580Humanname
329388122CV2468606single nucleotide variantNM_173672.5(PPIL6):c.26C>T (p.Pro9Leu)not specified [RCV004278166]uncertain significance6109440565109440565Humanname
405794462CV3366366single nucleotide variantNM_173672.5(PPIL6):c.14A>G (p.Gln5Arg)not specified [RCV004507068]uncertain significance6109440577109440577Humanname
405794468CV3366368single nucleotide variantNM_173672.5(PPIL6):c.26C>A (p.Pro9His)not specified [RCV004507070]uncertain significance6109440565109440565Humanname
598160319CV3897390single nucleotide variantNM_173672.5(PPIL6):c.23G>A (p.Gly8Glu)not specified [RCV005260957]uncertain significance6109440568109440568Humanname
329376322CV2425072single nucleotide variantNM_173672.5(PPIL6):c.68C>T (p.Pro23Leu)not specified [RCV004248968]uncertain significance6109440523109440523Humanname
329372785CV2428650single nucleotide variantNM_173672.5(PPIL6):c.50C>A (p.Pro17Gln)not specified [RCV004255450]likely benign6109440541109440541Humanname
329373769CV2434581single nucleotide variantNM_173672.5(PPIL6):c.95T>A (p.Phe32Tyr)not specified [RCV004254279]uncertain significance6109440496109440496Humanname
407482812CV3471439single nucleotide variantNM_173672.5(PPIL6):c.64C>T (p.Arg22Trp)not specified [RCV004664837]uncertain significance6109440527109440527Humanname
597757812CV3591250single nucleotide variantNM_173672.5(PPIL6):c.31C>T (p.His11Tyr)not specified [RCV004848399]uncertain significance6109440560109440560Humanname
156102218CV2367747single nucleotide variantNM_173672.5(PPIL6):c.133G>A (p.Glu45Lys)not specified [RCV004213705]uncertain significance6109440458109440458Humanname
401774281CV2727791single nucleotide variantNM_173672.5(PPIL6):c.146A>G (p.Asn49Ser)not specified [RCV004323817]likely benign6109436189109436189Humanname
401862393CV2775281single nucleotide variantNM_173672.5(PPIL6):c.263C>T (p.Ser88Phe)not specified [RCV004348401]uncertain significance6109431314109431314Humanname
405794465CV3366367single nucleotide variantNM_173672.5(PPIL6):c.199G>A (p.Ala67Thr)not specified [RCV004507069]uncertain significance6109436136109436136Humanname
407482824CV3471442single nucleotide variantNM_173672.5(PPIL6):c.184C>T (p.Pro62Ser)not specified [RCV004664839]uncertain significance6109436151109436151Humanname
598160313CV3897389single nucleotide variantNM_173672.5(PPIL6):c.284A>C (p.Asn95Thr)not specified [RCV005260956]uncertain significance6109431293109431293Humanname
156159822CV2236267single nucleotide variantNM_173672.5(PPIL6):c.430G>T (p.Val144Leu)not specified [RCV004107967]uncertain significance6109427147109427147Humanname
156114906CV2273246single nucleotide variantNM_173672.5(PPIL6):c.696C>A (p.Asn232Lys)not specified [RCV004132041]uncertain significance6109400163109400163Humanname
156006214CV2281800single nucleotide variantNM_173672.5(PPIL6):c.740A>G (p.Asn247Ser)not specified [RCV004147933]uncertain significance6109400119109400119Humanname
156271883CV2308666single nucleotide variantNM_173672.5(PPIL6):c.364G>A (p.Ala122Thr)not specified [RCV004167215]uncertain significance6109431213109431213Humanname
156166323CV2315225single nucleotide variantNM_173672.5(PPIL6):c.833T>C (p.Ile278Thr)not specified [RCV004165392]uncertain significance6109392929109392929Humanname
156136436CV2364944single nucleotide variantNM_173672.5(PPIL6):c.899T>C (p.Met300Thr)not specified [RCV004222239]uncertain significance6109392863109392863Humanname
156006098CV2401161single nucleotide variantNM_173672.5(PPIL6):c.463A>G (p.Ile155Val)not specified [RCV004245719]uncertain significance6109427114109427114Humanname
401864778CV2778039single nucleotide variantNM_173672.5(PPIL6):c.760G>A (p.Gly254Arg)not specified [RCV004347993]uncertain significance6109400099109400099Humanname
401899978CV2780140single nucleotide variantNM_173672.5(PPIL6):c.748C>T (p.Arg250Cys)not specified [RCV004355796]uncertain significance6109400111109400111Humanname
405794474CV3366370single nucleotide variantNM_173672.5(PPIL6):c.694A>G (p.Asn232Asp)not specified [RCV004507072]uncertain significance6109400165109400165Humanname
405794476CV3366371single nucleotide variantNM_173672.5(PPIL6):c.835G>A (p.Glu279Lys)not specified [RCV004507073]uncertain significance6109392927109392927Humanname
405854748CV3394863single nucleotide variantNM_173672.5(PPIL6):c.451G>A (p.Asp151Asn)not provided [RCV004555004]uncertain significance6109427126109427126Humanname
407529621CV3471441single nucleotide variantNM_173672.5(PPIL6):c.352A>C (p.Ile118Leu)not specified [RCV004656134]uncertain significance6109431225109431225Humanname
597757808CV3591249single nucleotide variantNM_173672.5(PPIL6):c.725T>C (p.Val242Ala)not specified [RCV004848398]uncertain significance6109400134109400134Humanname
597757817CV3591251single nucleotide variantNM_173672.5(PPIL6):c.673G>T (p.Gly225Cys)not specified [RCV004848400]uncertain significance6109419202109419202Humanname
598160323CV3897391single nucleotide variantNM_173672.5(PPIL6):c.657T>G (p.Asn219Lys)not specified [RCV005260958]uncertain significance6109419218109419218Humanname