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)

25 records found for search term Akap7
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401884334CV2762873single nucleotide variantNM_016377.4(AKAP7):c.25A>G (p.Ile9Val)not specified [RCV004340417]uncertain significance6131145290131145290Humanname
156289431CV2324804single nucleotide variantNM_016377.4(AKAP7):c.39G>C (p.Glu13Asp)not specified [RCV004173035]uncertain significance6131145304131145304Humanname
405791255CV3266971single nucleotide variantNM_016377.4(AKAP7):c.91A>G (p.Thr31Ala)not specified [RCV004399794]uncertain significance6131145356131145356Humanname
407512586CV3432865single nucleotide variantNM_016377.4(AKAP7):c.94A>G (p.Met32Val)not specified [RCV004626796]likely benign6131145359131145359Humanname
597699085CV3669716single nucleotide variantNM_016377.4(AKAP7):c.35A>G (p.Asn12Ser)not specified [RCV004916203]likely benign6131145300131145300Humanname
156017673CV2262933single nucleotide variantNM_016377.4(AKAP7):c.162A>T (p.Glu54Asp)not specified [RCV004125072]uncertain significance6131160069131160069Humanname
405791188CV3266947single nucleotide variantNM_016377.4(AKAP7):c.107T>G (p.Val36Gly)not specified [RCV004399770]uncertain significance6131145372131145372Humanname
407512406CV3432884single nucleotide variantNM_016377.4(AKAP7):c.209G>A (p.Ser70Asn)not specified [RCV004626813]uncertain significance6131160116131160116Humanname
407512435CV3432896single nucleotide variantNM_016377.4(AKAP7):c.207G>C (p.Lys69Asn)not specified [RCV004626822]uncertain significance6131160114131160114Humanname
597699034CV3669695single nucleotide variantNM_016377.4(AKAP7):c.143A>G (p.Asp48Gly)not specified [RCV004916197]uncertain significance6131145408131145408Humanname
156264720CV2275339single nucleotide variantNM_016377.4(AKAP7):c.572C>T (p.Ser191Leu)not specified [RCV004135229]uncertain significance6131169256131169256Humanname
156327084CV2332050single nucleotide variantNM_016377.4(AKAP7):c.979G>A (p.Glu327Lys)not specified [RCV004189101]uncertain significance6131281658131281658Humanname
329361811CV2468337single nucleotide variantNM_016377.4(AKAP7):c.895C>T (p.Leu299Phe)not specified [RCV004275884]uncertain significance6131281574131281574Humanname
401740000CV2709765single nucleotide variantNM_016377.4(AKAP7):c.394G>A (p.Val132Met)not specified [RCV004320749]uncertain significance6131165183131165183Humanname
401883403CV2761088single nucleotide variantNM_016377.4(AKAP7):c.772T>A (p.Tyr258Asn)not specified [RCV004338747]uncertain significance6131219730131219730Humanname
401894967CV2792632single nucleotide variantNM_016377.4(AKAP7):c.734A>C (p.Glu245Ala)not specified [RCV004363653]uncertain significance6131219692131219692Humanname
405791238CV3266965single nucleotide variantNM_016377.4(AKAP7):c.768A>G (p.Ile256Met)not specified [RCV004399788]likely benign6131219726131219726Humanname
597698926CV3669678single nucleotide variantNM_016377.4(AKAP7):c.778A>G (p.Ile260Val)not specified [RCV004916184]uncertain significance6131219736131219736Humanname
597699067CV3669700single nucleotide variantNM_016377.4(AKAP7):c.302G>T (p.Gly101Val)not specified [RCV004916201]uncertain significance6131165091131165091Humanname
597699076CV3669709single nucleotide variantNM_016377.4(AKAP7):c.667A>C (p.Met223Leu)not specified [RCV004916202]uncertain significance6131199538131199538Humanname
598199649CV3955360single nucleotide variantNM_016377.4(AKAP7):c.748C>T (p.His250Tyr)not specified [RCV005336521]uncertain significance6131219706131219706Humanname
407512376CV3432875single nucleotide variantNM_016377.4(AKAP7):c.1012C>G (p.Gln338Glu)not specified [RCV004626804]uncertain significance6131281691131281691Humanname
597699010CV3669688single nucleotide variantNM_016377.4(AKAP7):c.1003G>A (p.Ala335Thr)not specified [RCV004916194]uncertain significance6131281682131281682Humanname
597699635CV3669724single nucleotide variantNM_016377.4(AKAP7):c.1033A>G (p.Asn345Asp)not specified [RCV004916211]uncertain significance6131281712131281712Humanname
598199671CV3955364single nucleotide variantNM_016377.4(AKAP7):c.1032G>T (p.Glu344Asp)not specified [RCV005336525]likely benign6131281711131281711Humanname