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)

20 records found for search term Arl6ip5
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
598251673CV3902043single nucleotide variantNM_006407.4(ARL6IP5):c.7G>A (p.Val3Ile)not specified [RCV005259282]uncertain significance36908505469085054Humanname
401762604CV2719993single nucleotide variantNM_006407.4(ARL6IP5):c.20C>A (p.Pro7Gln)not specified [RCV004323575]uncertain significance36908506769085067Humanname
156368102CV2266941single nucleotide variantNM_006407.4(ARL6IP5):c.274C>T (p.Arg92Trp)not specified [RCV004131598]uncertain significance36910193669101936Humanname
156036747CV2332475single nucleotide variantNM_006407.4(ARL6IP5):c.236G>C (p.Gly79Ala)not specified [RCV004196200]uncertain significance36910189869101898Humanname
401755726CV2678749single nucleotide variantNM_006407.4(ARL6IP5):c.286C>T (p.Arg96Cys)not specified [RCV004292744]uncertain significance36910194869101948Humanname
405663018CV3290150single nucleotide variantNM_006407.4(ARL6IP5):c.226G>A (p.Val76Met)not specified [RCV004417923]uncertain significance36910188869101888Humanname
597705860CV3592955single nucleotide variantNM_006407.4(ARL6IP5):c.296C>T (p.Thr99Met)not specified [RCV004860443]uncertain significance36910195869101958Humanname
597783720CV3592962single nucleotide variantNM_006407.4(ARL6IP5):c.257A>G (p.Asn86Ser)not specified [RCV004854309]uncertain significance36910191969101919Humanname
597705891CV3592966single nucleotide variantNM_006407.4(ARL6IP5):c.206G>A (p.Gly69Glu)not specified [RCV004860446]uncertain significance36910186869101868Humanname
598251719CV3902052single nucleotide variantNM_006407.4(ARL6IP5):c.265G>A (p.Val89Ile)not specified [RCV005259291]likely benign36910192769101927Humanname
156137078CV2210355single nucleotide variantNM_006407.4(ARL6IP5):c.401T>C (p.Phe134Ser)not specified [RCV004089508]uncertain significance36910447069104470Humanname
156116824CV2283025single nucleotide variantNM_006407.4(ARL6IP5):c.438C>A (p.Asn146Lys)not specified [RCV004143646]uncertain significance36910450769104507Humanname
156054005CV2308628single nucleotide variantNM_006407.4(ARL6IP5):c.360G>A (p.Met120Ile)not specified [RCV004167183]uncertain significance36910202269102022Humanname
155911570CV2313349single nucleotide variantNM_006407.4(ARL6IP5):c.506T>A (p.Leu169Gln)not specified [RCV004163678]uncertain significance36910457569104575Humanname
329400732CV2438715single nucleotide variantNM_006407.4(ARL6IP5):c.545A>G (p.Tyr182Cys)not specified [RCV004261867]uncertain significance36910461469104614Humanname
405663023CV3290151single nucleotide variantNM_006407.4(ARL6IP5):c.434A>C (p.Lys145Thr)not specified [RCV004417924]uncertain significance36910450369104503Humanname
407513767CV3476188single nucleotide variantNM_006407.4(ARL6IP5):c.374G>A (p.Gly125Asp)not specified [RCV004674239]uncertain significance36910203669102036Humanname
407513772CV3476198single nucleotide variantNM_006407.4(ARL6IP5):c.310G>A (p.Val104Met)not specified [RCV004674241]uncertain significance36910197269101972Humanname
597705924CV3592972single nucleotide variantNM_006407.4(ARL6IP5):c.556G>A (p.Val186Met)not specified [RCV004860449]uncertain significance36910462569104625Humanname
597705977CV3592982single nucleotide variantNM_006407.4(ARL6IP5):c.550A>G (p.Ser184Gly)not specified [RCV004860454]uncertain significance36910461969104619Humanname