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 All species
(View Results for all Objects and Ontologies)

33 records found for search term Mtnr1a
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
150331552CV1171245deletionNM_005958.4(MTNR1A):c.185-154delnot provided [RCV001538678]benign4186534711186534711Humanname
156291305CV2236428single nucleotide variantNM_005958.4(MTNR1A):c.6G>C (p.Gln2His)not specified [RCV004108103]uncertain significance4186555360186555360Humanname
401862757CV2758900single nucleotide variantNM_005958.4(MTNR1A):c.13G>C (p.Gly5Arg)not specified [RCV004339982]uncertain significance4186555353186555353Humanname
150480680CV1239629single nucleotide variantNM_005958.4(MTNR1A):c.924A>G (p.Arg308=)not provided [RCV001652792]benign4186533818186533818Humanname
150506212CV1242158single nucleotide variantNM_005958.4(MTNR1A):c.945A>G (p.Thr315=)not provided [RCV001658511]benign4186533797186533797Humanname
405669039CV3369929single nucleotide variantNM_005958.4(MTNR1A):c.474C>T (p.Ala158=)not specified [RCV004514765]likely benign4186534268186534268Humanname
15123375CV764417single nucleotide variantNM_005958.4(MTNR1A):c.588C>T (p.Phe196=)not provided [RCV000940843]likely benign4186534154186534154Humanname
8625757CV80881single nucleotide variantNM_005958.3(MTNR1A):c.441C>T (p.Tyr147=)Malignant melanoma [RCV000060958]not provided4186534301186534301Humanname
8631128CV86284single nucleotide variantNM_005958.3(MTNR1A):c.594C>T (p.Val198=)Malignant melanoma [RCV000066375]not provided4186534148186534148Humanname
156123875CV2227292single nucleotide variantNM_005958.4(MTNR1A):c.274G>A (p.Gly92Arg)not specified [RCV004091849]uncertain significance4186534468186534468Humanname
156088407CV2359231single nucleotide variantNM_005958.4(MTNR1A):c.155T>C (p.Val52Ala)not specified [RCV004212524]uncertain significance4186555211186555211Humanname
401730852CV2674176single nucleotide variantNM_005958.4(MTNR1A):c.271A>T (p.Asn91Tyr)not specified [RCV004289073]uncertain significance4186534471186534471Humanname
597651391CV3561272single nucleotide variantNM_005958.4(MTNR1A):c.239C>T (p.Pro80Leu)not specified [RCV004833627]uncertain significance4186534503186534503Humanname
597651400CV3561273single nucleotide variantNM_005958.4(MTNR1A):c.158A>G (p.Tyr53Cys)not specified [RCV004833628]uncertain significance4186555208186555208Humanname
597651410CV3561274single nucleotide variantNM_005958.4(MTNR1A):c.260C>T (p.Ser87Leu)not specified [RCV004833629]uncertain significance4186534482186534482Humanname
598263493CV3986479single nucleotide variantNM_005958.4(MTNR1A):c.142G>A (p.Val48Ile)not specified [RCV005387466]uncertain significance4186555224186555224Humanname
156172372CV2286857single nucleotide variantNM_005958.4(MTNR1A):c.602T>A (p.Ile201Asn)not specified [RCV004142657]uncertain significance4186534140186534140Humanname
401780403CV2674009single nucleotide variantNM_005958.4(MTNR1A):c.337G>A (p.Gly113Ser)not specified [RCV004293375]uncertain significance4186534405186534405Humanname
405669011CV3369923single nucleotide variantNM_005958.4(MTNR1A):c.442G>A (p.Val148Met)not specified [RCV004514759]uncertain significance4186534300186534300Humanname
405669074CV3369936single nucleotide variantNM_005958.4(MTNR1A):c.698A>T (p.Asp233Val)not specified [RCV004514772]uncertain significance4186534044186534044Humanname
405669123CV3369946single nucleotide variantNM_005958.4(MTNR1A):c.839G>C (p.Ser280Thr)not specified [RCV004514782]uncertain significance4186533903186533903Humanname
405669146CV3369950single nucleotide variantNM_005958.4(MTNR1A):c.930A>G (p.Ile310Met)not specified [RCV004514786]uncertain significance4186533812186533812Humanname
405669159CV3369952single nucleotide variantNM_005958.4(MTNR1A):c.976G>A (p.Asp326Asn)not specified [RCV004514788]uncertain significance4186533766186533766Humanname
407507409CV3457663single nucleotide variantNM_005958.4(MTNR1A):c.506A>T (p.Gln169Leu)not specified [RCV004646804]uncertain significance4186534236186534236Humanname
597651379CV3561271single nucleotide variantNM_005958.4(MTNR1A):c.475G>A (p.Val159Ile)not specified [RCV004833626]likely benign4186534267186534267Humanname
598227665CV3986478single nucleotide variantNM_005958.4(MTNR1A):c.926T>C (p.Ile309Thr)not specified [RCV005380758]uncertain significance4186533816186533816Humanname
598227673CV3986480single nucleotide variantNM_005958.4(MTNR1A):c.392A>G (p.His131Arg)not specified [RCV005380759]uncertain significance4186534350186534350Humanname
598227683CV3986481single nucleotide variantNM_005958.4(MTNR1A):c.418A>T (p.Ser140Cys)not specified [RCV005380760]uncertain significance4186534324186534324Humanname
598263498CV3986482single nucleotide variantNM_005958.4(MTNR1A):c.361A>G (p.Ile121Val)not specified [RCV005387467]uncertain significance4186534381186534381Humanname
15181920CV709278single nucleotide variantNM_005958.4(MTNR1A):c.635T>C (p.Ile212Thr)not provided [RCV000974508]benign4186534107186534107Humanname
15194394CV720884single nucleotide variantNM_005958.4(MTNR1A):c.470C>T (p.Ala157Val)not provided [RCV000889212]benign4186534272186534272Humanname
8631127CV86283single nucleotide variantNM_005958.3(MTNR1A):c.595C>T (p.Pro199Ser)Malignant melanoma [RCV000066374]not provided4186534147186534147Humanname
155923800CV2351873single nucleotide variantNM_005958.4(MTNR1A):c.1033G>A (p.Val345Ile)not specified [RCV004198016]likely benign4186533709186533709Humanname