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)

26 records found for search term Chmp6
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15194025CV778559deletionNM_024591.5(CHMP6):c.495+14delnot provided [RCV000955533]benign178099734980997349Humanname
156088873CV2359300single nucleotide variantNM_024591.5(CHMP6):c.92G>A (p.Arg31Lys)not specified [RCV004212585]likely benign178099460980994609Humanname
401782113CV2719181single nucleotide variantNM_024591.5(CHMP6):c.35G>C (p.Arg12Pro)not specified [RCV004324844]uncertain significance178099195380991953Humanname
15201680CV704454single nucleotide variantNM_024591.5(CHMP6):c.555C>T (p.Asn185=)not provided [RCV000957693]benign178099910280999102Humanname
156399538CV2205180single nucleotide variantNM_024591.5(CHMP6):c.175C>T (p.Arg59Trp)not specified [RCV004077774]uncertain significance178099502080995020Humanname
155943441CV2298577single nucleotide variantNM_024591.5(CHMP6):c.133C>T (p.Arg45Cys)not specified [RCV004162227]uncertain significance178099465080994650Humanname
156268094CV2329731single nucleotide variantNM_024591.5(CHMP6):c.236A>C (p.Asn79Thr)not specified [RCV004180831]uncertain significance178099508180995081Humanname
155928567CV2388900single nucleotide variantNM_024591.5(CHMP6):c.145C>T (p.Arg49Trp)not specified [RCV004241905]uncertain significance178099466280994662Humanname
329393030CV2469189single nucleotide variantNM_024591.5(CHMP6):c.124G>C (p.Glu42Gln)not specified [RCV004280542]uncertain significance178099464180994641Humanname
405661933CV3297141single nucleotide variantNM_024591.5(CHMP6):c.134G>A (p.Arg45His)not specified [RCV004439338]uncertain significance178099465180994651Humanname
405661936CV3297142single nucleotide variantNM_024591.5(CHMP6):c.136G>A (p.Ala46Thr)not specified [RCV004439339]uncertain significance178099465380994653Humanname
407455727CV3422762single nucleotide variantNM_024591.5(CHMP6):c.262G>A (p.Val88Ile)not specified [RCV004610390]uncertain significance178099567280995672Humanname
597769837CV3653203single nucleotide variantNM_024591.5(CHMP6):c.158G>A (p.Arg53Gln)not specified [RCV004896811]uncertain significance178099467580994675Humanname
597769843CV3653204single nucleotide variantNM_024591.5(CHMP6):c.181A>G (p.Lys61Glu)not specified [RCV004896812]uncertain significance178099502680995026Humanname
15201752CV704453single nucleotide variantNM_024591.5(CHMP6):c.163G>A (p.Gly55Ser)not provided [RCV000957714]benign178099468080994680Humanname
156004073CV2254251single nucleotide variantNM_024591.5(CHMP6):c.413G>A (p.Arg138Gln)not specified [RCV004129927]uncertain significance178099707180997071Humanname
156046975CV2304310single nucleotide variantNM_024591.5(CHMP6):c.352A>G (p.Met118Val)not specified [RCV004164430]uncertain significance178099701080997010Humanname
156101309CV2347793single nucleotide variantNM_024591.5(CHMP6):c.569C>A (p.Ala190Asp)not specified [RCV004195451]uncertain significance178099911680999116Humanname
405661938CV3297143single nucleotide variantNM_024591.5(CHMP6):c.317T>C (p.Phe106Ser)not specified [RCV004439340]uncertain significance178099572780995727Humanname
405661941CV3297144single nucleotide variantNM_024591.5(CHMP6):c.389C>T (p.Thr130Met)not specified [RCV004439341]uncertain significance178099704780997047Humanname
405661943CV3297145single nucleotide variantNM_024591.5(CHMP6):c.418A>G (p.Ile140Val)not specified [RCV004439342]uncertain significance178099726480997264Humanname
407455723CV3422763single nucleotide variantNM_024591.5(CHMP6):c.301A>T (p.Met101Leu)not specified [RCV004610391]uncertain significance178099571180995711Humanname
597769827CV3653201single nucleotide variantNM_024591.5(CHMP6):c.400G>A (p.Val134Met)not specified [RCV004896809]uncertain significance178099705880997058Humanname
597769832CV3653202single nucleotide variantNM_024591.5(CHMP6):c.452A>T (p.Glu151Val)not specified [RCV004896810]uncertain significance178099729880997298Humanname
597769849CV3653205single nucleotide variantNM_024591.5(CHMP6):c.347A>G (p.Gln116Arg)not specified [RCV004896813]uncertain significance178099575780995757Humanname
598214824CV3951652single nucleotide variantNM_024591.5(CHMP6):c.358A>T (p.Ile120Phe)not specified [RCV005316639]uncertain significance178099701680997016Humanname