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)

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

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155971072CV2214058single nucleotide variantNM_007178.4(STRAP):c.7A>G (p.Met3Val)not specified [RCV004084104]uncertain significance121588271415882714Humanname
156175412CV2327142single nucleotide variantNM_007178.4(STRAP):c.32C>G (p.Ser11Cys)not specified [RCV004178707]uncertain significance121588273915882739Humanname
401857609CV2767035single nucleotide variantNM_007178.4(STRAP):c.67A>G (p.Ser23Gly)not specified [RCV004347447]uncertain significance121588277415882774Humanname
597758264CV3615058single nucleotide variantNM_007178.4(STRAP):c.68G>A (p.Ser23Asn)not specified [RCV004868766]uncertain significance121588277515882775Humanname
598208247CV3916002single nucleotide variantNM_007178.4(STRAP):c.70G>C (p.Gly24Arg)not specified [RCV005291430]uncertain significance121588277715882777Humanname
156241653CV2283117single nucleotide variantNM_007178.4(STRAP):c.104C>G (p.Ala35Gly)not specified [RCV004145809]uncertain significance121588281115882811Humanname
405779787CV3330878single nucleotide variantNM_007178.4(STRAP):c.253G>A (p.Val85Met)not specified [RCV004458456]uncertain significance121588993215889932Humanname
155970289CV2262213single nucleotide variantNM_007178.4(STRAP):c.446C>T (p.Ala149Val)not specified [RCV004126640]uncertain significance121589408915894089Humanname
156060441CV2305404single nucleotide variantNM_007178.4(STRAP):c.993A>C (p.Glu331Asp)not specified [RCV004171303]uncertain significance121590291815902918Humanname
156348944CV2309161single nucleotide variantNM_007178.4(STRAP):c.517A>G (p.Thr173Ala)not specified [RCV004171512]uncertain significance121589537515895375Humanname
401774349CV2727812single nucleotide variantNM_007178.4(STRAP):c.518C>G (p.Thr173Ser)not specified [RCV004323837]uncertain significance121589537615895376Humanname
405779793CV3330879single nucleotide variantNM_007178.4(STRAP):c.373C>T (p.Arg125Cys)not specified [RCV004458457]uncertain significance121589063915890639Humanname
407496609CV3485620single nucleotide variantNM_007178.4(STRAP):c.459T>G (p.Ser153Arg)not specified [RCV004668190]uncertain significance121589410215894102Humanname
598251815CV3916003single nucleotide variantNM_007178.4(STRAP):c.489C>A (p.Asp163Glu)not specified [RCV005277966]uncertain significance121589413215894132Humanname
598208251CV3916004single nucleotide variantNM_007178.4(STRAP):c.632C>T (p.Ala211Val)not specified [RCV005291431]uncertain significance121589549015895490Humanname
598208256CV3916005single nucleotide variantNM_007178.4(STRAP):c.574A>G (p.Ile192Val)not specified [RCV005291432]uncertain significance121589543215895432Humanname
8627242CV82386single nucleotide variantNM_007178.3(STRAP):c.345G>T (p.Leu115Phe)Malignant melanoma [RCV000062465]not provided121589061115890611Humanname