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)

27 records found for search term Bhlha15
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156157403CV2359953single nucleotide variantNM_177455.4(BHLHA15):c.16C>T (p.Arg6Trp)not specified [RCV004212796]uncertain significance79821232598212325Humanname
405728861CV3298262single nucleotide variantNM_177455.4(BHLHA15):c.25C>T (p.Arg9Trp)not specified [RCV004429083]uncertain significance79821233498212334Humanname
407472802CV3427559single nucleotide variantNM_177455.4(BHLHA15):c.17G>A (p.Arg6Gln)not specified [RCV004600209]uncertain significance79821232698212326Humanname
405728866CV3298263single nucleotide variantNM_177455.4(BHLHA15):c.58A>T (p.Thr20Ser)not specified [RCV004429084]uncertain significance79821236798212367Humanname
407472806CV3427560single nucleotide variantNM_177455.4(BHLHA15):c.32G>A (p.Arg11Gln)not specified [RCV004600210]uncertain significance79821234198212341Humanname
597738004CV3636579single nucleotide variantNM_177455.4(BHLHA15):c.43C>G (p.Gln15Glu)not specified [RCV004890047]uncertain significance79821235298212352Humanname
598276749CV3949404single nucleotide variantNM_177455.4(BHLHA15):c.74C>T (p.Thr25Met)not specified [RCV005305883]uncertain significance79821238398212383Humanname
598161225CV3949407single nucleotide variantNM_177455.4(BHLHA15):c.82G>C (p.Gly28Arg)not specified [RCV005306967]likely benign79821239198212391Humanname
156336106CV2228493single nucleotide variantNM_177455.4(BHLHA15):c.134C>T (p.Pro45Leu)not specified [RCV004092740]uncertain significance79821244398212443Humanname
156291157CV2236383single nucleotide variantNM_177455.4(BHLHA15):c.259C>T (p.Arg87Trp)not specified [RCV004108062]uncertain significance79821256898212568Humanname
156142850CV2268752single nucleotide variantNM_177455.4(BHLHA15):c.187C>A (p.Pro63Thr)not specified [RCV004124143]uncertain significance79821249698212496Humanname
156252873CV2283998single nucleotide variantNM_177455.4(BHLHA15):c.131G>A (p.Arg44Gln)not specified [RCV004144615]uncertain significance79821244098212440Humanname
155906192CV2303269single nucleotide variantNM_177455.4(BHLHA15):c.215G>C (p.Ser72Thr)not specified [RCV004159020]uncertain significance79821252498212524Humanname
156162941CV2368327single nucleotide variantNM_177455.4(BHLHA15):c.117G>T (p.Lys39Asn)not specified [RCV004219105]uncertain significance79821242698212426Humanname
401738196CV2676162single nucleotide variantNM_177455.4(BHLHA15):c.191C>T (p.Ser64Phe)not specified [RCV004284383]uncertain significance79821250098212500Humanname
405728831CV3298259single nucleotide variantNM_177455.4(BHLHA15):c.110C>T (p.Pro37Leu)not specified [RCV004429080]likely benign79821241998212419Humanname
405728840CV3298260single nucleotide variantNM_177455.4(BHLHA15):c.145G>T (p.Ala49Ser)not specified [RCV004429081]uncertain significance79821245498212454Humanname
405728846CV3298261single nucleotide variantNM_177455.4(BHLHA15):c.172C>T (p.Arg58Cys)not specified [RCV004429082]uncertain significance79821248198212481Humanname
407472809CV3427561single nucleotide variantNM_177455.4(BHLHA15):c.296G>A (p.Arg99His)not specified [RCV004600211]uncertain significance79821260598212605Humanname
597737992CV3636575single nucleotide variantNM_177455.4(BHLHA15):c.178C>T (p.Arg60Trp)not specified [RCV004890044]uncertain significance79821248798212487Humanname
597737994CV3636576single nucleotide variantNM_177455.4(BHLHA15):c.200G>A (p.Gly67Asp)not specified [RCV004890045]uncertain significance79821250998212509Humanname
598276750CV3949405single nucleotide variantNM_177455.4(BHLHA15):c.217A>G (p.Ser73Gly)not specified [RCV005305884]uncertain significance79821252698212526Humanname
156275359CV2255662single nucleotide variantNM_177455.4(BHLHA15):c.547C>T (p.His183Tyr)not specified [RCV004120065]uncertain significance79821285698212856Humanname
156344937CV2372842single nucleotide variantNM_177455.4(BHLHA15):c.524T>C (p.Leu175Pro)not specified [RCV004222024]uncertain significance79821283398212833Humanname
156210877CV2378220single nucleotide variantNM_177455.4(BHLHA15):c.541C>A (p.Gln181Lys)not specified [RCV004226259]uncertain significance79821285098212850Humanname
597737999CV3636577single nucleotide variantNM_177455.4(BHLHA15):c.511C>T (p.Pro171Ser)not specified [RCV004890046]uncertain significance79821282098212820Humanname
598276751CV3949406single nucleotide variantNM_177455.4(BHLHA15):c.488C>T (p.Ala163Val)not specified [RCV005305885]uncertain significance79821279798212797Humanname