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Variants search result for Homo sapiens
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66 records found for search term Capn11
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15160664CV735688single nucleotide variantNM_007058.4(CAPN11):c.6G>A (p.Leu2=)not provided [RCV000903190]benign64415885444158854Humanname
401856801CV2760880single nucleotide variantNM_007058.4(CAPN11):c.74G>C (p.Arg25Pro)not specified [RCV004336515]uncertain significance64416681544166815Humanname
407480488CV3424616single nucleotide variantNM_007058.4(CAPN11):c.85G>C (p.Ala29Pro)not specified [RCV004600765]uncertain significance64416682644166826Humanname
15098513CV699608single nucleotide variantNM_007058.4(CAPN11):c.453C>T (p.Cys151=)not provided [RCV000958578]benign64417234544172345Humanname
155988500CV2259577single nucleotide variantNM_007058.4(CAPN11):c.136C>T (p.Arg46Trp)not specified [RCV004116624]uncertain significance64416932844169328Humanname
156297027CV2319241single nucleotide variantNM_007058.4(CAPN11):c.283A>G (p.Lys95Glu)not specified [RCV004178286]uncertain significance64416947544169475Humanname
156013202CV2359037single nucleotide variantNM_007058.4(CAPN11):c.166G>A (p.Asp56Asn)not specified [RCV004212360]uncertain significance64416935844169358Humanname
156094042CV2398788single nucleotide variantNM_007058.4(CAPN11):c.107C>T (p.Thr36Met)not specified [RCV004243815]uncertain significance64416929944169299Humanname
401747864CV2731954single nucleotide variantNM_007058.4(CAPN11):c.137G>A (p.Arg46Gln)not specified [RCV004333193]uncertain significance64416932944169329Humanname
407480473CV3424613single nucleotide variantNM_007058.4(CAPN11):c.158G>A (p.Gly53Asp)not specified [RCV004600762]uncertain significance64416935044169350Humanname
597764576CV3647689single nucleotide variantNM_007058.4(CAPN11):c.241G>A (p.Glu81Lys)not specified [RCV004895658]uncertain significance64416943344169433Humanname
598163782CV3943139single nucleotide variantNM_007058.4(CAPN11):c.248C>G (p.Pro83Arg)not specified [RCV005307437]uncertain significance64416944044169440Humanname
156137110CV2357314single nucleotide variantNM_007058.4(CAPN11):c.709G>A (p.Gly237Ser)not specified [RCV004200206]uncertain significance64417326444173264Humanname
155998376CV2393419single nucleotide variantNM_007058.4(CAPN11):c.470G>A (p.Arg157His)not specified [RCV004228916]uncertain significance64417236244172362Humanname
329349466CV2435833single nucleotide variantNM_007058.4(CAPN11):c.733G>A (p.Val245Met)not specified [RCV004255073]uncertain significance64417328844173288Humanname
401748450CV2708608single nucleotide variantNM_007058.4(CAPN11):c.473T>G (p.Val158Gly)not specified [RCV004307596]uncertain significance64417236544172365Humanname
401857649CV2770933single nucleotide variantNM_007058.4(CAPN11):c.370G>A (p.Asp124Asn)not specified [RCV004343601]likely benign64416993644169936Humanname
405711416CV3298871single nucleotide variantNM_007058.4(CAPN11):c.448A>T (p.Thr150Ser)not specified [RCV004426870]uncertain significance64417234044172340Humanname
405711431CV3298873single nucleotide variantNM_007058.4(CAPN11):c.498G>C (p.Lys166Asn)not specified [RCV004426872]uncertain significance64417239044172390Humanname
405711438CV3298874single nucleotide variantNM_007058.4(CAPN11):c.514A>G (p.Ile172Val)not specified [RCV004426873]uncertain significance64417240644172406Humanname
405711445CV3298875single nucleotide variantNM_007058.4(CAPN11):c.718G>A (p.Asp240Asn)not specified [RCV004426874]uncertain significance64417327344173273Humanname
405711451CV3298876single nucleotide variantNM_007058.4(CAPN11):c.818G>C (p.Gly273Ala)not specified [RCV004426875]uncertain significance64417337344173373Humanname
405711461CV3298877single nucleotide variantNM_007058.4(CAPN11):c.968G>A (p.Gly323Asp)not specified [RCV004426876]uncertain significance64417630544176305Humanname
407480461CV3424611single nucleotide variantNM_007058.4(CAPN11):c.392T>C (p.Ile131Thr)not specified [RCV004600760]uncertain significance64416995844169958Humanname
407480480CV3424615single nucleotide variantNM_007058.4(CAPN11):c.472G>A (p.Val158Met)not specified [RCV004600764]uncertain significance64417236444172364Humanname
407480500CV3424618single nucleotide variantNM_007058.4(CAPN11):c.671G>A (p.Gly224Glu)not specified [RCV004600767]uncertain significance64417322644173226Humanname
597764564CV3647685single nucleotide variantNM_007058.4(CAPN11):c.602T>C (p.Phe201Ser)not specified [RCV004895655]uncertain significance64417301344173013Humanname
597764568CV3647687single nucleotide variantNM_007058.4(CAPN11):c.391A>G (p.Ile131Val)not specified [RCV004895656]likely benign64416995744169957Humanname
597764580CV3647690single nucleotide variantNM_007058.4(CAPN11):c.306A>C (p.Lys102Asn)not specified [RCV004895659]uncertain significance64416949844169498Humanname
597764591CV3647694single nucleotide variantNM_007058.4(CAPN11):c.563T>G (p.Val188Gly)not specified [RCV004895662]uncertain significance64417297444172974Humanname
597764595CV3647695single nucleotide variantNM_007058.4(CAPN11):c.817G>T (p.Gly273Cys)not specified [RCV004895663]uncertain significance64417337244173372Humanname
598163769CV3943137single nucleotide variantNM_007058.4(CAPN11):c.955C>T (p.Arg319Trp)not specified [RCV005307435]uncertain significance64417629244176292Humanname
15191512CV735689single nucleotide variantNM_007058.4(CAPN11):c.397C>T (p.Gln133Ter)not provided [RCV000910268]likely benign64416996344169963Humanname
156401258CV2210768single nucleotide variantNM_007058.4(CAPN11):c.1198C>T (p.Arg400Cys)not specified [RCV004085863]uncertain significance64417695944176959Humanname
156379623CV2211476single nucleotide variantNM_007058.4(CAPN11):c.1864A>C (p.Met622Leu)not specified [RCV004084388]uncertain significance64418099244180992Humanname
155927518CV2218401single nucleotide variantNM_007058.4(CAPN11):c.1066G>A (p.Gly356Arg)not specified [RCV004090695]uncertain significance64417664544176645Humanname
155971643CV2238650single nucleotide variantNM_007058.4(CAPN11):c.1853T>C (p.Met618Thr)not specified [RCV004107553]uncertain significance64418098144180981Humanname
155918914CV2254761single nucleotide variantNM_007058.4(CAPN11):c.1469T>C (p.Phe490Ser)not specified [RCV004115231]uncertain significance64417999244179992Humanname
156368298CV2266977single nucleotide variantNM_007058.4(CAPN11):c.1003G>T (p.Ala335Ser)not specified [RCV004131626]likely benign64417658244176582Humanname
156193659CV2302008single nucleotide variantNM_007058.4(CAPN11):c.1245C>G (p.Phe415Leu)not specified [RCV004158778]uncertain significance64417724944177249Humanname
155952528CV2306132single nucleotide variantNM_007058.4(CAPN11):c.1478A>G (p.Tyr493Cys)not specified [RCV004162885]uncertain significance64418000144180001Humanname
156056166CV2320591single nucleotide variantNM_007058.4(CAPN11):c.1321G>A (p.Val441Ile)not specified [RCV004172212]uncertain significance64417732544177325Humanname
156185011CV2324628single nucleotide variantNM_007058.4(CAPN11):c.1235C>G (p.Pro412Arg)not specified [RCV004172880]uncertain significance64417699644176996Humanname
156165780CV2348624single nucleotide variantNM_007058.4(CAPN11):c.1186G>C (p.Glu396Gln)not specified [RCV004195849]uncertain significance64417694744176947Humanname
155990603CV2352503single nucleotide variantNM_007058.4(CAPN11):c.2170C>T (p.His724Tyr)not specified [RCV004203007]likely benign64418374044183740Humanname
156191027CV2356815single nucleotide variantNM_007058.4(CAPN11):c.2089T>G (p.Phe697Val)not specified [RCV004603343]uncertain significance64418319044183190Humanname
156402467CV2361485single nucleotide variantNM_007058.4(CAPN11):c.1133C>T (p.Thr378Met)not specified [RCV004221124]uncertain significance64417689444176894Humanname
329349715CV2424552single nucleotide variantNM_007058.4(CAPN11):c.1084T>C (p.Tyr362His)not specified [RCV004254053]uncertain significance64417684544176845Humanname
329349585CV2424933single nucleotide variantNM_007058.4(CAPN11):c.1058C>T (p.Thr353Met)not specified [RCV004248807]likely benign64417663744176637Humanname
329349735CV2443051single nucleotide variantNM_007058.4(CAPN11):c.1369C>T (p.Arg457Trp)not specified [RCV004253639]uncertain significance64417737344177373Humanname
401746968CV2675434single nucleotide variantNM_007058.4(CAPN11):c.1525A>C (p.Ser509Arg)not specified [RCV004292234]uncertain significance64418004844180048Humanname
401746306CV2708962single nucleotide variantNM_007058.4(CAPN11):c.1372C>A (p.Gln458Lys)not specified [RCV004309926]uncertain significance64417737644177376Humanname
405711393CV3298868single nucleotide variantNM_007058.4(CAPN11):c.1414G>A (p.Ala472Thr)not specified [RCV004426867]uncertain significance64417741844177418Humanname
405711411CV3298870single nucleotide variantNM_007058.4(CAPN11):c.1735G>A (p.Val579Met)not specified [RCV004426869]uncertain significance64418065144180651Humanname
407480448CV3424609single nucleotide variantNM_007058.4(CAPN11):c.1997G>T (p.Arg666Leu)not specified [RCV004600758]uncertain significance64418299944182999Humanname
407480455CV3424610single nucleotide variantNM_007058.4(CAPN11):c.1199G>A (p.Arg400His)not specified [RCV004600759]uncertain significance64417696044176960Humanname
407480467CV3424612single nucleotide variantNM_007058.4(CAPN11):c.1876G>T (p.Gly626Cys)not specified [RCV004600761]uncertain significance64418125844181258Humanname
407480492CV3424617single nucleotide variantNM_007058.4(CAPN11):c.2107T>C (p.Cys703Arg)not specified [RCV004600766]uncertain significance64418320844183208Humanname
597764560CV3647684single nucleotide variantNM_007058.4(CAPN11):c.1759G>A (p.Gly587Arg)not specified [RCV004895654]uncertain significance64418076044180760Humanname
597764572CV3647688single nucleotide variantNM_007058.4(CAPN11):c.1997G>A (p.Arg666His)not specified [RCV004895657]uncertain significance64418299944182999Humanname
597764584CV3647691single nucleotide variantNM_007058.4(CAPN11):c.1999C>A (p.Leu667Met)not specified [RCV004895660]uncertain significance64418300144183001Humanname
597764587CV3647692single nucleotide variantNM_007058.4(CAPN11):c.1726T>C (p.Phe576Leu)not specified [RCV004895661]uncertain significance64418064244180642Humanname
597750915CV3647693single nucleotide variantNM_007058.4(CAPN11):c.1360C>T (p.Arg454Trp)not specified [RCV004892656]uncertain significance64417736444177364Humanname
598212839CV3943136single nucleotide variantNM_007058.4(CAPN11):c.1942A>G (p.Ile648Val)not specified [RCV005316226]uncertain significance64418294444182944Humanname
598163775CV3943138single nucleotide variantNM_007058.4(CAPN11):c.1303G>A (p.Ala435Thr)not specified [RCV005307436]likely benign64417730744177307Humanname
598163789CV3943140single nucleotide variantNM_007058.4(CAPN11):c.1213G>C (p.Ala405Pro)not specified [RCV005307438]uncertain significance64417697444176974Humanname