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91 records found for search term Itih3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15098952CV698239single nucleotide variantNM_002217.4(ITIH3):c.165C>T (p.Thr55=)not provided [RCV000958671]benign35279653152796531Humanname
156369301CV2193941single nucleotide variantNM_002217.4(ITIH3):c.82C>T (p.Arg28Trp)not specified [RCV004074671]uncertain significance35279488552794885Humanname
401768226CV2675174single nucleotide variantNM_002217.4(ITIH3):c.97C>T (p.Arg33Trp)not specified [RCV004289948]uncertain significance35279560652795606Humanname
598171423CV3972877single nucleotide variantNM_002217.4(ITIH3):c.71G>A (p.Arg24Lys)not specified [RCV005370582]uncertain significance35279487452794874Humanname
598171452CV3972884single nucleotide variantNM_002217.4(ITIH3):c.83G>A (p.Arg28Gln)not specified [RCV005370587]uncertain significance35279488652794886Humanname
15111180CV748439single nucleotide variantNM_002217.4(ITIH3):c.456C>T (p.Phe152=)not provided [RCV000916679]benign35279717452797174Humanname
8630906CV86062single nucleotide variantNM_002217.3(ITIH3):c.396G>A (p.Gly132=)Malignant melanoma [RCV000066146]not provided35279711452797114Humanname
156185646CV2251699single nucleotide variantNM_002217.4(ITIH3):c.251C>A (p.Pro84His)not specified [RCV004119710]uncertain significance35279661752796617Humanname
156369048CV2263254single nucleotide variantNM_002217.4(ITIH3):c.220G>A (p.Ala74Thr)not specified [RCV004131753]uncertain significance35279658652796586Humanname
155989753CV2282866single nucleotide variantNM_002217.4(ITIH3):c.292G>A (p.Gly98Ser)not specified [RCV004143517]uncertain significance35279674952796749Humanname
156177506CV2327188single nucleotide variantNM_002217.4(ITIH3):c.170G>A (p.Arg57His)not specified [RCV004174654]uncertain significance35279653652796536Humanname
156292508CV2340167single nucleotide variantNM_002217.4(ITIH3):c.181A>G (p.Asn61Asp)not specified [RCV004192404]uncertain significance35279654752796547Humanname
329364834CV2443946single nucleotide variantNM_002217.4(ITIH3):c.130G>A (p.Glu44Lys)not specified [RCV004258275]uncertain significance35279649652796496Humanname
405785835CV3268263single nucleotide variantNM_002217.4(ITIH3):c.202G>A (p.Val68Ile)not specified [RCV004398448]uncertain significance35279656852796568Humanname
405785853CV3268266single nucleotide variantNM_002217.4(ITIH3):c.218C>T (p.Thr73Met)not specified [RCV004398451]uncertain significance35279658452796584Humanname
407459180CV3451779single nucleotide variantNM_002217.4(ITIH3):c.146A>C (p.Lys49Thr)not specified [RCV004633527]uncertain significance35279651252796512Humanname
597794007CV3687133single nucleotide variantNM_002217.4(ITIH3):c.208C>T (p.Arg70Cys)not specified [RCV004934391]uncertain significance35279657452796574Humanname
15183907CV708983single nucleotide variantNM_002217.4(ITIH3):c.1023C>T (p.Pro341=)not provided [RCV000974985]benign35279986952799869Humanname
15106064CV748440single nucleotide variantNM_002217.4(ITIH3):c.2145C>T (p.Ile715=)not provided [RCV000915671]likely benign35280698952806989Humanname
150445440CV1269435single nucleotide variantNM_002217.4(ITIH3):c.943C>A (p.Gln315Lys)not provided [RCV001691123]benign35279978952799789Human11name
150445440CV1269435single nucleotide variantNM_002217.4(ITIH3):c.943C>A (p.Gln315Lys)not provided [RCV001691123]benign35279978952799790Human11name
156286021CV2334897single nucleotide variantNM_002217.4(ITIH3):c.422C>T (p.Ser141Leu)not specified [RCV004182003]uncertain significance35279714052797140Humanname
155974986CV2342616single nucleotide variantNM_002217.4(ITIH3):c.701G>A (p.Arg234His)not specified [RCV004196705]uncertain significance35279900352799003Humanname
156215361CV2347852single nucleotide variantNM_002217.4(ITIH3):c.760G>A (p.Val254Met)not specified [RCV004195503]uncertain significance35279906252799062Humanname
156150295CV2359598single nucleotide variantNM_002217.4(ITIH3):c.634G>A (p.Ala212Thr)not specified [RCV004214898]uncertain significance35279790152797901Humanname
329367386CV2427318single nucleotide variantNM_002217.4(ITIH3):c.871A>T (p.Ile291Phe)not specified [RCV004248178]uncertain significance35279945352799453Humanname
329381126CV2440660single nucleotide variantNM_002217.4(ITIH3):c.892C>T (p.Arg298Trp)not specified [RCV004256568]uncertain significance35279947452799474Humanname
329392164CV2470436single nucleotide variantNM_002217.4(ITIH3):c.775C>T (p.Pro259Ser)not specified [RCV004273464]uncertain significance35279907752799077Humanname
401723183CV2674737single nucleotide variantNM_002217.4(ITIH3):c.508T>C (p.Tyr170His)not specified [RCV004294022]uncertain significance35279722652797226Humanname
401867059CV2780066single nucleotide variantNM_002217.4(ITIH3):c.797A>G (p.Asn266Ser)not specified [RCV004355730]uncertain significance35279937952799379Humanname
401882919CV2788674single nucleotide variantNM_002217.4(ITIH3):c.656G>C (p.Gly219Ala)not specified [RCV004361154]uncertain significance35279792352797923Humanname
405785864CV3268269single nucleotide variantNM_002217.4(ITIH3):c.317A>C (p.Lys106Thr)not specified [RCV004398454]uncertain significance35279677452796774Humanname
405785869CV3268270single nucleotide variantNM_002217.4(ITIH3):c.893G>A (p.Arg298Gln)not specified [RCV004398455]uncertain significance35279947552799475Humanname
597793996CV3687129single nucleotide variantNM_002217.4(ITIH3):c.877G>A (p.Gly293Ser)not specified [RCV004934387]uncertain significance35279945952799459Humanname
597793998CV3687130single nucleotide variantNM_002217.4(ITIH3):c.944A>G (p.Gln315Arg)not specified [RCV004934388]uncertain significance35279979052799790Humanname
597794004CV3687132single nucleotide variantNM_002217.4(ITIH3):c.978T>G (p.Ser326Arg)not specified [RCV004934390]uncertain significance35279982452799824Humanname
598171417CV3972876single nucleotide variantNM_002217.4(ITIH3):c.365G>A (p.Gly122Asp)not specified [RCV005370581]uncertain significance35279682252796822Humanname
156234744CV2193331single nucleotide variantNM_002217.4(ITIH3):c.1748C>A (p.Ala583Asp)not specified [RCV004072835]uncertain significance35280389352803893Humanname
156261501CV2204907single nucleotide variantNM_002217.4(ITIH3):c.1091A>T (p.Asp364Val)not specified [RCV004075148]uncertain significance35280055352800553Humanname
156322527CV2205111single nucleotide variantNM_002217.4(ITIH3):c.2048C>T (p.Ala683Val)not specified [RCV004077711]uncertain significance35280639852806398Humanname
156189065CV2205891single nucleotide variantNM_002217.4(ITIH3):c.1343G>A (p.Arg448Gln)not specified [RCV004078327]uncertain significance35280110652801106Humanname
156276255CV2209757single nucleotide variantNM_002217.4(ITIH3):c.2266T>A (p.Ser756Thr)not specified [RCV004083073]uncertain significance35280775152807751Humanname
156007100CV2289025single nucleotide variantNM_002217.4(ITIH3):c.1948G>C (p.Gly650Arg)not specified [RCV004149974]uncertain significance35280629852806298Humanname
155987087CV2354856single nucleotide variantNM_002217.4(ITIH3):c.1148C>G (p.Pro383Arg)not specified [RCV004191354]uncertain significance35280061052800610Humanname
156402240CV2363621single nucleotide variantNM_002217.4(ITIH3):c.1189G>A (p.Asp397Asn)not provided [RCV004695719]|not specified [RCV004216574]uncertain significance35280065152800651Humanname
156385741CV2364552single nucleotide variantNM_002217.4(ITIH3):c.1883T>C (p.Val628Ala)not specified [RCV004217409]uncertain significance35280581752805817Humanname
156046525CV2385351single nucleotide variantNM_002217.4(ITIH3):c.2033G>A (p.Arg678His)not specified [RCV004230624]uncertain significance35280638352806383Humanname
156216628CV2386082single nucleotide variantNM_002217.4(ITIH3):c.1726G>A (p.Glu576Lys)not specified [RCV004229139]uncertain significance35280387152803871Humanname
155957497CV2387502single nucleotide variantNM_002217.4(ITIH3):c.1418C>T (p.Thr473Met)not specified [RCV004240358]uncertain significance35280236852802368Humanname
156082627CV2394778single nucleotide variantNM_002217.4(ITIH3):c.2356C>G (p.Pro786Ala)not specified [RCV004234447]uncertain significance35280784152807841Humanname
329399122CV2439461single nucleotide variantNM_002217.4(ITIH3):c.1675G>T (p.Ala559Ser)not specified [RCV004249749]uncertain significance35280277252802772Humanname
329391699CV2444945single nucleotide variantNM_002217.4(ITIH3):c.1216G>A (p.Glu406Lys)not specified [RCV004261572]uncertain significance35280097952800979Humanname
329378134CV2459155single nucleotide variantNM_002217.4(ITIH3):c.2239A>G (p.Thr747Ala)not specified [RCV004272606]uncertain significance35280708352807083Humanname
401736125CV2672829single nucleotide variantNM_002217.4(ITIH3):c.2473C>T (p.Arg825Trp)not specified [RCV004281605]uncertain significance35280815152808151Humanname
401738272CV2676187single nucleotide variantNM_002217.4(ITIH3):c.1318G>T (p.Ala440Ser)not specified [RCV004284404]uncertain significance35280108152801081Humanname
401722313CV2676935single nucleotide variantNM_002217.4(ITIH3):c.1939T>C (p.Tyr647His)not specified [RCV004293539]uncertain significance35280613552806135Humanname
401752503CV2682842single nucleotide variantNM_002217.4(ITIH3):c.1536G>C (p.Met512Ile)not specified [RCV004283645]uncertain significance35280248652802486Humanname
401770385CV2711131single nucleotide variantNM_002217.4(ITIH3):c.1519C>A (p.Leu507Met)not specified [RCV004310812]uncertain significance35280246952802469Humanname
401737984CV2714278single nucleotide variantNM_002217.4(ITIH3):c.2323G>A (p.Val775Met)not specified [RCV004315963]uncertain significance35280780852807808Humanname
401783352CV2727878single nucleotide variantNM_002217.4(ITIH3):c.2489C>T (p.Pro830Leu)not specified [RCV004323892]uncertain significance35280816752808167Humanname
401870605CV2769304single nucleotide variantNM_002217.4(ITIH3):c.1676C>A (p.Ala559Asp)not specified [RCV004357305]uncertain significance35280277352802773Humanname
405785811CV3268258single nucleotide variantNM_002217.4(ITIH3):c.1528G>C (p.Glu510Gln)not specified [RCV004398443]uncertain significance35280247852802478Humanname
405785816CV3268259single nucleotide variantNM_002217.4(ITIH3):c.1556T>G (p.Val519Gly)not specified [RCV004398444]uncertain significance35280250652802506Humanname
405785821CV3268260single nucleotide variantNM_002217.4(ITIH3):c.1642T>C (p.Tyr548His)not specified [RCV004398445]uncertain significance35280273952802739Humanname
405785825CV3268261single nucleotide variantNM_002217.4(ITIH3):c.1687A>G (p.Ile563Val)not specified [RCV004398446]uncertain significance35280278452802784Humanname
405785830CV3268262single nucleotide variantNM_002217.4(ITIH3):c.1930C>G (p.Pro644Ala)not specified [RCV004398447]uncertain significance35280612652806126Humanname
405785840CV3268264single nucleotide variantNM_002217.4(ITIH3):c.2071G>T (p.Gly691Trp)not specified [RCV004398449]uncertain significance35280691552806915Humanname
405785845CV3268265single nucleotide variantNM_002217.4(ITIH3):c.2183C>T (p.Thr728Met)not specified [RCV004398450]uncertain significance35280702752807027Humanname
405785856CV3268267single nucleotide variantNM_002217.4(ITIH3):c.2402G>A (p.Arg801Gln)not specified [RCV004398452]uncertain significance35280788752807887Humanname
405785860CV3268268single nucleotide variantNM_002217.4(ITIH3):c.2471T>A (p.Ile824Asn)not specified [RCV004398453]uncertain significance35280814952808149Humanname
407459162CV3451773single nucleotide variantNM_002217.4(ITIH3):c.1345C>T (p.Arg449Cys)not specified [RCV004633521]uncertain significance35280110852801108Humanname
407459168CV3451775single nucleotide variantNM_002217.4(ITIH3):c.2062A>G (p.Thr688Ala)not specified [RCV004633523]uncertain significance35280690652806906Humanname
407459171CV3451776single nucleotide variantNM_002217.4(ITIH3):c.1093G>A (p.Gly365Arg)not specified [RCV004633524]uncertain significance35280055552800555Humanname
407459174CV3451777single nucleotide variantNM_002217.4(ITIH3):c.2441T>C (p.Phe814Ser)not specified [RCV004633525]uncertain significance35280811952808119Humanname
407459177CV3451778single nucleotide variantNM_002217.4(ITIH3):c.1931C>A (p.Pro644His)not specified [RCV004633526]uncertain significance35280612752806127Humanname
597793976CV3687122single nucleotide variantNM_002217.4(ITIH3):c.2072G>C (p.Gly691Ala)not specified [RCV004934380]uncertain significance35280691652806916Humanname
597793979CV3687123single nucleotide variantNM_002217.4(ITIH3):c.1196A>G (p.Asn399Ser)not specified [RCV004934381]uncertain significance35280065852800658Humanname
597793982CV3687124single nucleotide variantNM_002217.4(ITIH3):c.1637G>A (p.Arg546Gln)not specified [RCV004934382]likely benign35280273452802734Humanname
597793987CV3687126single nucleotide variantNM_002217.4(ITIH3):c.2008G>A (p.Asp670Asn)not specified [RCV004934384]likely benign35280635852806358Humanname
597793990CV3687127single nucleotide variantNM_002217.4(ITIH3):c.2401C>T (p.Arg801Trp)not specified [RCV004934385]uncertain significance35280788652807886Humanname
597793993CV3687128single nucleotide variantNM_002217.4(ITIH3):c.2224T>A (p.Phe742Ile)not specified [RCV004934386]uncertain significance35280706852807068Humanname
597794001CV3687131single nucleotide variantNM_002217.4(ITIH3):c.1667G>A (p.Arg556Gln)not specified [RCV004934389]uncertain significance35280276452802764Humanname
597794010CV3687134single nucleotide variantNM_002217.4(ITIH3):c.1504G>A (p.Val502Met)not specified [RCV004934392]uncertain significance35280245452802454Humanname
598171434CV3972879single nucleotide variantNM_002217.4(ITIH3):c.1896G>A (p.Met632Ile)not specified [RCV005370584]uncertain significance35280583052805830Humanname
598171441CV3972880single nucleotide variantNM_002217.4(ITIH3):c.2105A>G (p.Asp702Gly)not specified [RCV005370585]uncertain significance35280694952806949Humanname
598258037CV3972881single nucleotide variantNM_002217.4(ITIH3):c.2459A>T (p.Lys820Ile)not specified [RCV005347113]uncertain significance35280813752808137Humanname
598211495CV3972882single nucleotide variantNM_002217.4(ITIH3):c.1981A>G (p.Lys661Glu)not specified [RCV005358691]uncertain significance35280633152806331Humanname
598171447CV3972883single nucleotide variantNM_002217.4(ITIH3):c.1441G>A (p.Glu481Lys)not specified [RCV005370586]uncertain significance35280239152802391Humanname
15193254CV698240single nucleotide variantNM_002217.4(ITIH3):c.1567G>A (p.Gly523Arg)not provided [RCV000955317]benign35280251752802517Human2name
15193254CV698240single nucleotide variantNM_002217.4(ITIH3):c.1567G>A (p.Gly523Arg)not provided [RCV000955317]benign35280251752802518Human2name
15156666CV698241single nucleotide variantNM_002217.4(ITIH3):c.2251A>G (p.Thr751Ala)not provided [RCV000946742]benign35280709552807095Humanname