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Variants search result for Homo sapiens
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54 records found for search term Prkcq
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597779398CV3591532single nucleotide variantNM_006257.5(PRKCQ):c.8C>T (p.Pro3Leu)not specified [RCV004853251]uncertain significance1065151286515128Humanname
597749562CV3591531single nucleotide variantNM_006257.5(PRKCQ):c.17G>T (p.Arg6Leu)not specified [RCV004846251]uncertain significance1065151196515119Humanname
156190306CV2391063single nucleotide variantNM_006257.5(PRKCQ):c.65G>A (p.Gly22Asp)not specified [RCV004235055]uncertain significance1065150716515071Humanname
405671083CV3378250single nucleotide variantNM_006257.5(PRKCQ):c.47C>T (p.Ser16Phe)not specified [RCV004515175]uncertain significance1065150896515089Humanname
598246655CV3904497single nucleotide variantNM_006257.5(PRKCQ):c.97G>A (p.Val33Ile)not specified [RCV005258521]uncertain significance1065150396515039Humanname
156173927CV2326837single nucleotide variantNM_006257.5(PRKCQ):c.251A>C (p.Glu84Ala)not specified [RCV004176668]uncertain significance1065110626511062Humanname
156048587CV2391019single nucleotide variantNM_006257.5(PRKCQ):c.200G>A (p.Gly67Glu)not specified [RCV004235017]uncertain significance1065111136511113Humanname
401874692CV2759322single nucleotide variantNM_006257.5(PRKCQ):c.188A>G (p.His63Arg)not specified [RCV004335906]uncertain significance1065111256511125Humanname
401886620CV2776661single nucleotide variantNM_006257.5(PRKCQ):c.163C>T (p.Pro55Ser)not specified [RCV004357831]uncertain significance1065111506511150Humanname
597749532CV3591525single nucleotide variantNM_006257.5(PRKCQ):c.130A>G (p.Met44Val)not specified [RCV004846245]uncertain significance1065111836511183Humanname
15141898CV712429single nucleotide variantNM_006257.5(PRKCQ):c.1326G>A (p.Thr442=)not provided [RCV000966382]benign1064790196479019Humanname
8633692CV88906single nucleotide variantNM_006257.5(PRKCQ):c.125G>A (p.Gly42Glu)not specified [RCV004349690]uncertain significance|not provided1065111886511188Humanname
155925277CV2277271single nucleotide variantNM_006257.5(PRKCQ):c.943C>G (p.Pro315Ala)not specified [RCV004142886]uncertain significance1064852276485227Humanname
155970396CV2335578single nucleotide variantNM_006257.5(PRKCQ):c.407C>T (p.Thr136Met)not specified [RCV004193786]uncertain significance1064985316498531Humanname
155936115CV2379769single nucleotide variantNM_006257.5(PRKCQ):c.961C>A (p.Pro321Thr)not specified [RCV004219885]uncertain significance1064852096485209Humanname
329402749CV2451318single nucleotide variantNM_006257.5(PRKCQ):c.397G>A (p.Glu133Lys)not specified [RCV004272012]uncertain significance1064985416498541Humanname
401761165CV2706241single nucleotide variantNM_006257.5(PRKCQ):c.352A>C (p.Asn118His)not specified [RCV004314910]uncertain significance1065074636507463Humanname
405671071CV3378247single nucleotide variantNM_006257.5(PRKCQ):c.378T>A (p.Ser126Arg)not specified [RCV004515172]uncertain significance1065074376507437Humanname
405671077CV3378249single nucleotide variantNM_006257.5(PRKCQ):c.411A>T (p.Glu137Asp)not specified [RCV004515174]uncertain significance1064985276498527Humanname
405671087CV3378251single nucleotide variantNM_006257.5(PRKCQ):c.919A>G (p.Thr307Ala)not specified [RCV004515176]uncertain significance1064852516485251Humanname
597749537CV3591526single nucleotide variantNM_006257.5(PRKCQ):c.469G>A (p.Val157Ile)not specified [RCV004846246]uncertain significance1064984696498469Humanname
597749547CV3591528single nucleotide variantNM_006257.5(PRKCQ):c.399A>C (p.Glu133Asp)not specified [RCV004846248]uncertain significance1064985396498539Humanname
597749557CV3591530single nucleotide variantNM_006257.5(PRKCQ):c.674G>A (p.Arg225Lys)not specified [RCV004846250]uncertain significance1064917996491799Humanname
14399424CV578028single nucleotide variantNM_006257.5(PRKCQ):c.989C>T (p.Pro330Leu)Inflammatory bowel disease 1 [RCV001784354]|not provided [RCV001672927]pathogenic|benign1064851816485181Human2name
15152876CV737551single nucleotide variantNM_006257.5(PRKCQ):c.640A>G (p.Ile214Val)not provided [RCV000901655]benign1064970556497055Humanname
156230011CV2199539single nucleotide variantNM_006257.5(PRKCQ):c.1073A>G (p.His358Arg)not specified [RCV004071091]uncertain significance1064835466483546Humanname
156388623CV2231924single nucleotide variantNM_006257.5(PRKCQ):c.1222A>G (p.Ile408Val)not specified [RCV004092996]uncertain significance1064791236479123Humanname
156134665CV2284679single nucleotide variantNM_006257.5(PRKCQ):c.1774C>G (p.Arg592Gly)not specified [RCV004140832]uncertain significance1064419556441955Humanname
156191684CV2289366single nucleotide variantNM_006257.5(PRKCQ):c.1651T>G (p.Leu551Val)not specified [RCV004152333]uncertain significance1064420786442078Humanname
156198545CV2293701single nucleotide variantNM_006257.5(PRKCQ):c.1045C>T (p.Pro349Ser)not specified [RCV004154991]uncertain significance1064835746483574Humanname
156001231CV2391873single nucleotide variantNM_006257.5(PRKCQ):c.1904G>A (p.Arg635Gln)not specified [RCV004235746]uncertain significance1064308716430871Humanname
156159831CV2398145single nucleotide variantNM_006257.5(PRKCQ):c.1599T>G (p.Asp533Glu)not specified [RCV004241722]uncertain significance1064567226456722Humanname
329368763CV2450408single nucleotide variantNM_006257.5(PRKCQ):c.2103G>A (p.Met701Ile)not specified [RCV004265338]uncertain significance1064282256428225Humanname
401737313CV2699724single nucleotide variantNM_006257.5(PRKCQ):c.1357A>C (p.Asn453His)not specified [RCV004308065]uncertain significance1064644016464401Humanname
401730701CV2711454single nucleotide variantNM_006257.5(PRKCQ):c.1219G>A (p.Ala407Thr)not specified [RCV004306779]uncertain significance1064791266479126Humanname
401878352CV2774248single nucleotide variantNM_006257.5(PRKCQ):c.1870G>A (p.Val624Met)not specified [RCV004347616]uncertain significance1064309056430905Humanname
401897085CV2789805single nucleotide variantNM_006257.5(PRKCQ):c.1135G>A (p.Asp379Asn)not specified [RCV004362200]uncertain significance1064834846483484Humanname
405671038CV3378240single nucleotide variantNM_006257.5(PRKCQ):c.1030A>G (p.Ile344Val)not specified [RCV004515165]uncertain significance1064835896483589Humanname
405671043CV3378241single nucleotide variantNM_006257.5(PRKCQ):c.1063A>G (p.Lys355Glu)not specified [RCV004515166]uncertain significance1064835566483556Humanname
405671052CV3378243single nucleotide variantNM_006257.5(PRKCQ):c.1228G>T (p.Ala410Ser)not specified [RCV004515168]uncertain significance1064791176479117Humanname
405671057CV3378244single nucleotide variantNM_006257.5(PRKCQ):c.1705C>T (p.Leu569Phe)not specified [RCV004515169]uncertain significance1064420246442024Humanname
405671067CV3378246single nucleotide variantNM_006257.5(PRKCQ):c.2020C>T (p.Arg674Trp)not specified [RCV004515171]uncertain significance1064283086428308Humanname
407513107CV3464361single nucleotide variantNM_006257.5(PRKCQ):c.1328A>G (p.His443Arg)not specified [RCV004648664]uncertain significance1064790176479017Humanname
407465315CV3464362single nucleotide variantNM_006257.5(PRKCQ):c.1001C>G (p.Pro334Arg)not specified [RCV004660202]uncertain significance1064851696485169Humanname
407513109CV3464363single nucleotide variantNM_006257.5(PRKCQ):c.1831G>T (p.Val611Leu)not specified [RCV004648665]uncertain significance1064418986441898Humanname
597749528CV3591524single nucleotide variantNM_006257.5(PRKCQ):c.1007C>T (p.Pro336Leu)not specified [RCV004846244]uncertain significance1064851636485163Humanname
597749542CV3591527single nucleotide variantNM_006257.5(PRKCQ):c.1074T>A (p.His358Gln)not specified [RCV004846247]uncertain significance1064835456483545Humanname
597749552CV3591529single nucleotide variantNM_006257.5(PRKCQ):c.1163A>G (p.Lys388Arg)not specified [RCV004846249]uncertain significance1064834566483456Humanname
597779402CV3591533single nucleotide variantNM_006257.5(PRKCQ):c.1922A>C (p.Glu641Ala)not specified [RCV004853252]uncertain significance1064308536430853Humanname
597779405CV3591534single nucleotide variantNM_006257.5(PRKCQ):c.1327C>T (p.His443Tyr)not specified [RCV004853253]uncertain significance1064790186479018Humanname
598246663CV3904498single nucleotide variantNM_006257.5(PRKCQ):c.1958C>T (p.Pro653Leu)not specified [RCV005258522]uncertain significance1064308176430817Humanname
598246668CV3904499single nucleotide variantNM_006257.5(PRKCQ):c.1945C>T (p.Pro649Ser)not specified [RCV005258523]uncertain significance1064308306430830Humanname
598246676CV3904500single nucleotide variantNM_006257.5(PRKCQ):c.1025A>C (p.Gln342Pro)not specified [RCV005258524]uncertain significance1064835946483594Humanname
15198594CV701403single nucleotide variantNM_006257.5(PRKCQ):c.1436C>G (p.Ser479Cys)not provided [RCV000956804]benign1064643226464322Humanname