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58 records found for search term Tmem62
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407526845CV3482791single nucleotide variantNM_024956.4(TMEM62):c.4G>C (p.Ala2Pro)not specified [RCV004679784]uncertain significance154313380643133806Humanname
405771710CV3346633single nucleotide variantNM_024956.4(TMEM62):c.23G>A (p.Arg8Lys)not specified [RCV004470404]uncertain significance154313382543133825Humanname
405771719CV3346635single nucleotide variantNM_024956.4(TMEM62):c.69G>C (p.Leu23Phe)not specified [RCV004470406]uncertain significance154313387143133871Humanname
597800576CV3610600single nucleotide variantNM_024956.4(TMEM62):c.98C>G (p.Ser33Trp)not specified [RCV004880282]uncertain significance154313390043133900Humanname
597800589CV3610606single nucleotide variantNM_024956.4(TMEM62):c.63G>A (p.Met21Ile)not specified [RCV004880288]uncertain significance154313386543133865Humanname
156045650CV2234511single nucleotide variantNM_024956.4(TMEM62):c.104T>C (p.Leu35Pro)not specified [RCV004100708]uncertain significance154313390643133906Humanname
156105737CV2361320single nucleotide variantNM_024956.4(TMEM62):c.148C>T (p.Pro50Ser)not specified [RCV004218528]uncertain significance154313395043133950Humanname
156251532CV2394314single nucleotide variantNM_024956.4(TMEM62):c.275C>T (p.Ala92Val)not specified [RCV004238537]uncertain significance154313435143134351Humanname
405771702CV3346632single nucleotide variantNM_024956.4(TMEM62):c.211G>C (p.Asp71His)not specified [RCV004470403]uncertain significance154313428743134287Humanname
597800591CV3610607single nucleotide variantNM_024956.4(TMEM62):c.218G>A (p.Gly73Asp)not specified [RCV004880289]uncertain significance154313429443134294Humanname
598227248CV3913978single nucleotide variantNM_024956.4(TMEM62):c.197T>G (p.Leu66Arg)not specified [RCV005294556]uncertain significance154313427343134273Humanname
598227258CV3913981single nucleotide variantNM_024956.4(TMEM62):c.269A>C (p.Gln90Pro)not specified [RCV005294558]uncertain significance154313434543134345Humanname
598227271CV3913983single nucleotide variantNM_024956.4(TMEM62):c.155A>G (p.Asp52Gly)not specified [RCV005294560]uncertain significance154313395743133957Humanname
598227278CV3913984single nucleotide variantNM_024956.4(TMEM62):c.110G>T (p.Arg37Leu)not specified [RCV005294561]uncertain significance154313391243133912Humanname
156082373CV2333551single nucleotide variantNM_024956.4(TMEM62):c.566C>T (p.Thr189Ile)not specified [RCV004190237]uncertain significance154314658243146582Humanname
156088126CV2337867single nucleotide variantNM_024956.4(TMEM62):c.464A>G (p.Lys155Arg)not specified [RCV004183877]uncertain significance154313860743138607Humanname
156205194CV2385174single nucleotide variantNM_024956.4(TMEM62):c.682T>C (p.Phe228Leu)not specified [RCV004228427]uncertain significance154314881843148818Humanname
329399921CV2444381single nucleotide variantNM_024956.4(TMEM62):c.784G>A (p.Gly262Ser)not specified [RCV004263126]uncertain significance154314906943149069Humanname
401763791CV2717123single nucleotide variantNM_024956.4(TMEM62):c.771T>A (p.His257Gln)not specified [RCV004324006]uncertain significance154314905643149056Humanname
401897791CV2772919single nucleotide variantNM_024956.4(TMEM62):c.688C>G (p.His230Asp)not specified [RCV004357690]uncertain significance154314882443148824Humanname
405771716CV3346634single nucleotide variantNM_024956.4(TMEM62):c.367G>A (p.Gly123Ser)not specified [RCV004470405]likely benign154313558643135586Humanname
407526842CV3482789single nucleotide variantNM_024956.4(TMEM62):c.937G>C (p.Val313Leu)not specified [RCV004679783]uncertain significance154315186043151860Humanname
597800580CV3610602single nucleotide variantNM_024956.4(TMEM62):c.332C>T (p.Ser111Phe)not specified [RCV004880284]uncertain significance154313555143135551Humanname
597800585CV3610604single nucleotide variantNM_024956.4(TMEM62):c.623A>C (p.Lys208Thr)not specified [RCV004880286]uncertain significance154314875943148759Humanname
597800587CV3610605single nucleotide variantNM_024956.4(TMEM62):c.401C>A (p.Thr134Asn)not specified [RCV004880287]uncertain significance154313562043135620Humanname
597800593CV3610608single nucleotide variantNM_024956.4(TMEM62):c.765T>G (p.Cys255Trp)not specified [RCV004880290]uncertain significance154314905043149050Humanname
598227253CV3913980single nucleotide variantNM_024956.4(TMEM62):c.545C>T (p.Ser182Leu)not specified [RCV005294557]uncertain significance154314656143146561Humanname
598227265CV3913982single nucleotide variantNM_024956.4(TMEM62):c.314C>T (p.Thr105Ile)not specified [RCV005294559]uncertain significance154313553343135533Humanname
155913968CV2242558single nucleotide variantNM_024956.4(TMEM62):c.1306C>T (p.Leu436Phe)not specified [RCV004113626]uncertain significance154316960243169602Humanname
156092690CV2302531single nucleotide variantNM_024956.4(TMEM62):c.1864G>A (p.Val622Met)not specified [RCV004161251]uncertain significance154318451843184518Humanname
156285499CV2334849single nucleotide variantNM_024956.4(TMEM62):c.1208T>C (p.Val403Ala)not specified [RCV004181958]likely benign154316070643160706Humanname
156141125CV2358379single nucleotide variantNM_024956.4(TMEM62):c.1001T>C (p.Leu334Pro)not specified [RCV004207274]uncertain significance154315192443151924Humanname
156104182CV2363540single nucleotide variantNM_024956.4(TMEM62):c.1361G>A (p.Arg454Gln)not specified [RCV004216109]uncertain significance154316965743169657Humanname
156245751CV2396721single nucleotide variantNM_024956.4(TMEM62):c.1375C>T (p.Leu459Phe)not specified [RCV004233875]uncertain significance154316967143169671Humanname
156195298CV2400479single nucleotide variantNM_024956.4(TMEM62):c.1337C>T (p.Thr446Ile)not specified [RCV004246680]uncertain significance154316963343169633Humanname
329393510CV2467048single nucleotide variantNM_024956.4(TMEM62):c.1579A>T (p.Ile527Leu)not specified [RCV004282788]likely benign154318127343181273Humanname
401725263CV2697337single nucleotide variantNM_024956.4(TMEM62):c.1289A>G (p.Tyr430Cys)not specified [RCV004304092]likely benign154316078743160787Humanname
401732151CV2708690single nucleotide variantNM_024956.4(TMEM62):c.1183G>A (p.Asp395Asn)not specified [RCV004307666]uncertain significance154316068143160681Humanname
401721499CV2709990single nucleotide variantNM_024956.4(TMEM62):c.1888T>A (p.Phe630Ile)not specified [RCV004315056]uncertain significance154318454243184542Humanname
405771660CV3346625single nucleotide variantNM_024956.4(TMEM62):c.1202A>T (p.Lys401Met)not specified [RCV004470396]uncertain significance154316070043160700Humanname
405771666CV3346626single nucleotide variantNM_024956.4(TMEM62):c.1236T>G (p.Asn412Lys)not specified [RCV004470397]uncertain significance154316073443160734Humanname
405771673CV3346627single nucleotide variantNM_024956.4(TMEM62):c.1487G>T (p.Gly496Val)not specified [RCV004470398]uncertain significance154318118143181181Humanname
405771679CV3346628single nucleotide variantNM_024956.4(TMEM62):c.1588A>G (p.Ile530Val)not specified [RCV004470399]likely benign154318128243181282Humanname
405771684CV3346629single nucleotide variantNM_024956.4(TMEM62):c.1663T>A (p.Cys555Ser)not specified [RCV004470400]uncertain significance154318431743184317Humanname
405771690CV3346630single nucleotide variantNM_024956.4(TMEM62):c.1792G>T (p.Gly598Cys)not specified [RCV004470401]uncertain significance154318444643184446Humanname
405771696CV3346631single nucleotide variantNM_024956.4(TMEM62):c.1832T>C (p.Leu611Ser)not specified [RCV004470402]uncertain significance154318448643184486Humanname
407458814CV3482787single nucleotide variantNM_024956.4(TMEM62):c.1817C>G (p.Pro606Arg)not specified [RCV004686948]uncertain significance154318447143184471Humanname
407526838CV3482788single nucleotide variantNM_024956.4(TMEM62):c.1889T>C (p.Phe630Ser)not specified [RCV004679782]uncertain significance154318454343184543Humanname
407458819CV3482790single nucleotide variantNM_024956.4(TMEM62):c.1136C>G (p.Pro379Arg)not specified [RCV004686949]uncertain significance154315478543154785Humanname
597800578CV3610601single nucleotide variantNM_024956.4(TMEM62):c.1042T>A (p.Ser348Thr)not specified [RCV004880283]uncertain significance154315469143154691Humanname
597800583CV3610603single nucleotide variantNM_024956.4(TMEM62):c.1700G>T (p.Arg567Ile)not specified [RCV004880285]uncertain significance154318435443184354Humanname
598227226CV3913975single nucleotide variantNM_024956.4(TMEM62):c.1835C>T (p.Thr612Ile)not specified [RCV005294553]uncertain significance154318448943184489Humanname
598227233CV3913976single nucleotide variantNM_024956.4(TMEM62):c.1126A>C (p.Lys376Gln)not specified [RCV005294554]uncertain significance154315477543154775Humanname
598227239CV3913977single nucleotide variantNM_024956.4(TMEM62):c.1277G>A (p.Arg426His)not specified [RCV005294555]uncertain significance154316077543160775Humanname
598252613CV3913979single nucleotide variantNM_024956.4(TMEM62):c.1723G>A (p.Val575Ile)not specified [RCV005278114]uncertain significance154318437743184377Humanname
598227284CV3913985single nucleotide variantNM_024956.4(TMEM62):c.1361G>C (p.Arg454Pro)not specified [RCV005294562]uncertain significance154316965743169657Humanname
598227291CV3913986single nucleotide variantNM_024956.4(TMEM62):c.1280C>T (p.Thr427Ile)not specified [RCV005294563]uncertain significance154316077843160778Humanname
598227301CV3913990single nucleotide variantNM_024956.4(TMEM62):c.1384C>T (p.Pro462Ser)not specified [RCV005294565]uncertain significance154317860943178609Humanname