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)

18 records found for search term Bcl6b
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
598201551CV3938604single nucleotide variantNM_181844.4(BCL6B):c.24G>C (p.Glu8Asp)not specified [RCV005314251]uncertain significance1770236957023695Humanname
8636326CV91549single nucleotide variantNM_181844.3(BCL6B):c.285C>T (p.Phe95=)Malignant melanoma [RCV000071647]not provided1770241887024188Humanname
156250033CV2394163single nucleotide variantNM_181844.4(BCL6B):c.38A>G (p.Tyr13Cys)not specified [RCV004236360]uncertain significance1770237097023709Humanname
405707753CV3297904single nucleotide variantNM_181844.4(BCL6B):c.37T>C (p.Tyr13His)not specified [RCV004426332]uncertain significance1770237087023708Humanname
405707738CV3297902single nucleotide variantNM_181844.4(BCL6B):c.100C>T (p.Arg34Cys)not specified [RCV004426330]uncertain significance1770237717023771Humanname
407499903CV3417695single nucleotide variantNM_181844.4(BCL6B):c.193T>C (p.Ser65Pro)not specified [RCV004607013]uncertain significance1770240967024096Humanname
598276596CV3938602single nucleotide variantNM_181844.4(BCL6B):c.122C>T (p.Thr41Met)not specified [RCV005305730]uncertain significance1770237937023793Humanname
8636327CV91550single nucleotide variantNM_181844.3(BCL6B):c.1350C>T (p.Phe450=)Malignant melanoma [RCV000071648]not provided1770275267027526Humanname
156189916CV2255095single nucleotide variantNM_181844.4(BCL6B):c.625G>C (p.Ala209Pro)not specified [RCV004115727]uncertain significance1770246247024624Humanname
156362262CV2265500single nucleotide variantNM_181844.4(BCL6B):c.693C>G (p.Asp231Glu)not specified [RCV004124253]uncertain significance1770246927024692Humanname
156058903CV2322969single nucleotide variantNM_181844.4(BCL6B):c.311C>G (p.Ser104Cys)not specified [RCV004185410]uncertain significance1770242147024214Humanname
329390658CV2440303single nucleotide variantNM_181844.4(BCL6B):c.428G>A (p.Arg143His)not specified [RCV004262784]uncertain significance1770244277024427Humanname
401863469CV2765829single nucleotide variantNM_181844.4(BCL6B):c.476G>A (p.Gly159Asp)not specified [RCV004335822]uncertain significance1770244757024475Humanname
401892413CV2781906single nucleotide variantNM_181844.4(BCL6B):c.367G>T (p.Val123Leu)not specified [RCV004357149]uncertain significance1770242707024270Humanname
405707745CV3297903single nucleotide variantNM_181844.4(BCL6B):c.325C>T (p.Pro109Ser)not specified [RCV004426331]uncertain significance1770242287024228Humanname
597737215CV3639703single nucleotide variantNM_181844.4(BCL6B):c.326C>G (p.Pro109Arg)not specified [RCV004889754]uncertain significance1770242297024229Humanname
598276595CV3938601single nucleotide variantNM_181844.4(BCL6B):c.544C>T (p.Pro182Ser)not specified [RCV005305729]uncertain significance1770245437024543Humanname
598201548CV3938603single nucleotide variantNM_181844.4(BCL6B):c.536A>G (p.Gln179Arg)not specified [RCV005314250]uncertain significance1770245357024535Humanname