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Variants search result for Homo sapiens
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59 records found for search term Actr5
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156270718CV2286179single nucleotide variantNM_024855.4(ACTR5):c.38C>T (p.Ala13Val)not specified [RCV004146147]uncertain significance203874851638748516Humanname
155983030CV2344265single nucleotide variantNM_024855.4(ACTR5):c.68C>T (p.Pro23Leu)not specified [RCV004195033]uncertain significance203874854638748546Humanname
156207810CV2360475single nucleotide variantNM_024855.4(ACTR5):c.76C>T (p.His26Tyr)not specified [RCV004208794]uncertain significance203874855438748554Humanname
405775152CV3296582single nucleotide variantNM_024855.4(ACTR5):c.82C>T (p.Pro28Ser)not specified [RCV004435975]uncertain significance203874856038748560Humanname
405775165CV3296584single nucleotide variantNM_024855.4(ACTR5):c.89C>T (p.Pro30Leu)not specified [RCV004435977]uncertain significance203874856738748567Humanname
405775007CV3300451single nucleotide variantNM_024855.4(ACTR5):c.40G>A (p.Ala14Thr)not specified [RCV004435952]uncertain significance203874851838748518Humanname
407497679CV3424831single nucleotide variantNM_024855.4(ACTR5):c.31G>A (p.Ala11Thr)not specified [RCV004606433]uncertain significance203874850938748509Humanname
597775956CV3644135single nucleotide variantNM_024855.4(ACTR5):c.52G>A (p.Val18Met)not specified [RCV004898362]uncertain significance203874853038748530Humanname
156184972CV2222566single nucleotide variantNM_024855.4(ACTR5):c.242G>A (p.Gly81Glu)not specified [RCV004099398]uncertain significance203874872038748720Humanname
156389654CV2226482single nucleotide variantNM_024855.4(ACTR5):c.146C>G (p.Pro49Arg)not specified [RCV004099684]uncertain significance203874862438748624Humanname
156081385CV2249056single nucleotide variantNM_024855.4(ACTR5):c.166G>A (p.Glu56Lys)not specified [RCV004116334]uncertain significance203874864438748644Humanname
329377483CV2451820single nucleotide variantNM_024855.4(ACTR5):c.257G>A (p.Ser86Asn)not specified [RCV004276502]uncertain significance203874873538748735Humanname
401870878CV2788931single nucleotide variantNM_024855.4(ACTR5):c.269T>A (p.Leu90Gln)not specified [RCV004363253]uncertain significance203874874738748747Humanname
597776066CV3644171single nucleotide variantNM_024855.4(ACTR5):c.163C>T (p.Pro55Ser)not specified [RCV004898389]uncertain significance203874864138748641Humanname
597776074CV3644179single nucleotide variantNM_024855.4(ACTR5):c.229G>A (p.Gly77Ser)not specified [RCV004898391]uncertain significance203874870738748707Humanname
598202550CV3946634single nucleotide variantNM_024855.4(ACTR5):c.145C>T (p.Pro49Ser)not specified [RCV005314482]uncertain significance203874862338748623Humanname
156399882CV2202282single nucleotide variantNM_024855.4(ACTR5):c.791G>A (p.Arg264Gln)not specified [RCV004078215]uncertain significance203875497238754972Humanname
156377870CV2207576single nucleotide variantNM_024855.4(ACTR5):c.910C>T (p.Arg304Trp)not specified [RCV004090365]uncertain significance203875509138755091Humanname
156079927CV2292644single nucleotide variantNM_024855.4(ACTR5):c.901C>G (p.Gln301Glu)not specified [RCV004154332]uncertain significance203875508238755082Humanname
156222321CV2343937single nucleotide variantNM_024855.4(ACTR5):c.467A>G (p.Tyr156Cys)not specified [RCV004195557]uncertain significance203875010138750101Humanname
156185462CV2377850single nucleotide variantNM_024855.4(ACTR5):c.509G>C (p.Ser170Thr)not specified [RCV004230426]uncertain significance203875014338750143Humanname
156262477CV2390873single nucleotide variantNM_024855.4(ACTR5):c.709A>G (p.Ile237Val)not specified [RCV004234893]uncertain significance203875223438752234Humanname
156003994CV2400940single nucleotide variantNM_024855.4(ACTR5):c.935G>A (p.Arg312Gln)not specified [RCV004244229]uncertain significance203875511638755116Humanname
329369036CV2450505single nucleotide variantNM_024855.4(ACTR5):c.822C>G (p.His274Gln)not specified [RCV004265423]uncertain significance203875500338755003Humanname
401726936CV2674608single nucleotide variantNM_024855.4(ACTR5):c.757G>A (p.Ala253Thr)not specified [RCV004291478]uncertain significance203875228238752282Humanname
401750372CV2696035single nucleotide variantNM_024855.4(ACTR5):c.725T>G (p.Met242Arg)not specified [RCV004308289]uncertain significance203875225038752250Humanname
401882231CV2774749single nucleotide variantNM_024855.4(ACTR5):c.883C>G (p.Gln295Glu)not specified [RCV004343849]uncertain significance203875506438755064Humanname
405775177CV3296586single nucleotide variantNM_024855.4(ACTR5):c.967C>T (p.Arg323Cys)not specified [RCV004435979]uncertain significance203875514838755148Humanname
405775050CV3300458single nucleotide variantNM_024855.4(ACTR5):c.505T>C (p.Phe169Leu)not specified [RCV004435959]uncertain significance203875013938750139Humanname
405775066CV3300461single nucleotide variantNM_024855.4(ACTR5):c.508A>G (p.Ser170Gly)not specified [RCV004435962]uncertain significance203875014238750142Humanname
407497713CV3424838single nucleotide variantNM_024855.4(ACTR5):c.890G>A (p.Arg297Lys)not specified [RCV004606440]uncertain significance203875507138755071Humanname
407497830CV3424870single nucleotide variantNM_024855.4(ACTR5):c.502C>T (p.Leu168Phe)not specified [RCV004606465]uncertain significance203875013638750136Humanname
407497932CV3424898single nucleotide variantNM_024855.4(ACTR5):c.703G>A (p.Ala235Thr)not specified [RCV004606491]uncertain significance203875222838752228Humanname
597775816CV3644093single nucleotide variantNM_024855.4(ACTR5):c.926A>G (p.Asn309Ser)not specified [RCV004898330]uncertain significance203875510738755107Humanname
597775886CV3644115single nucleotide variantNM_024855.4(ACTR5):c.932G>A (p.Arg311Gln)not specified [RCV004898346]uncertain significance203875511338755113Humanname
597775925CV3644125single nucleotide variantNM_024855.4(ACTR5):c.365T>A (p.Val122Asp)not specified [RCV004898355]uncertain significance203874884338748843Humanname
597760143CV3644137single nucleotide variantNM_024855.4(ACTR5):c.314A>G (p.Asn105Ser)not specified [RCV004894703]uncertain significance203874879238748792Humanname
598202478CV3946612single nucleotide variantNM_024855.4(ACTR5):c.724A>G (p.Met242Val)not specified [RCV005314466]uncertain significance203875224938752249Humanname
598202508CV3946619single nucleotide variantNM_024855.4(ACTR5):c.544A>G (p.Ser182Gly)not specified [RCV005314471]uncertain significance203875017838750178Humanname
598202592CV3946644single nucleotide variantNM_024855.4(ACTR5):c.425T>A (p.Leu142Gln)not specified [RCV005314490]uncertain significance203875005938750059Humanname
598212308CV3946655single nucleotide variantNM_024855.4(ACTR5):c.466T>C (p.Tyr156His)not specified [RCV005316150]uncertain significance203875010038750100Humanname
155953011CV2264296single nucleotide variantNM_024855.4(ACTR5):c.1784G>A (p.Gly595Asp)not specified [RCV004138219]uncertain significance203877177638771776Humanname
156289424CV2299348single nucleotide variantNM_024855.4(ACTR5):c.1487G>A (p.Gly496Asp)not specified [RCV004152658]uncertain significance203876751738767517Humanname
156043140CV2305782single nucleotide variantNM_024855.4(ACTR5):c.1594G>A (p.Asp532Asn)not specified [RCV004167588]uncertain significance203877158638771586Humanname
156211343CV2306146single nucleotide variantNM_024855.4(ACTR5):c.1642A>G (p.Asn548Asp)not specified [RCV004162897]likely benign203877163438771634Humanname
329374057CV2443623single nucleotide variantNM_024855.4(ACTR5):c.1245G>C (p.Leu415Phe)not specified [RCV004255931]uncertain significance203876547038765470Humanname
401864845CV2791388single nucleotide variantNM_024855.4(ACTR5):c.1276C>T (p.Pro426Ser)not specified [RCV004358789]uncertain significance203876550138765501Humanname
405774719CV3300402single nucleotide variantNM_024855.4(ACTR5):c.1061C>T (p.Pro354Leu)not specified [RCV004435903]uncertain significance203875592438755924Humanname
405774846CV3300424single nucleotide variantNM_024855.4(ACTR5):c.1613G>A (p.Arg538His)not specified [RCV004435925]uncertain significance203877160538771605Humanname
407497765CV3424850single nucleotide variantNM_024855.4(ACTR5):c.1122A>T (p.Lys374Asn)not specified [RCV004606450]uncertain significance203875598538755985Humanname
407497797CV3424860single nucleotide variantNM_024855.4(ACTR5):c.1349G>A (p.Arg450Gln)not specified [RCV004606457]uncertain significance203876629338766293Humanname
407497865CV3424880single nucleotide variantNM_024855.4(ACTR5):c.1412C>T (p.Thr471Ile)not specified [RCV004606474]uncertain significance203876635638766356Humanname
407454662CV3424888single nucleotide variantNM_024855.4(ACTR5):c.1805G>A (p.Gly602Asp)not specified [RCV004609934]uncertain significance203877179738771797Humanname
597775860CV3644104single nucleotide variantNM_024855.4(ACTR5):c.1606G>A (p.Gly536Ser)not specified [RCV004898340]uncertain significance203877159838771598Humanname
597775964CV3644142single nucleotide variantNM_024855.4(ACTR5):c.1142A>G (p.Asn381Ser)not specified [RCV004898364]likely benign203875600538756005Humanname
597776010CV3644153single nucleotide variantNM_024855.4(ACTR5):c.1112C>T (p.Ala371Val)not specified [RCV004898375]uncertain significance203875597538755975Humanname
597776038CV3644163single nucleotide variantNM_024855.4(ACTR5):c.1622C>G (p.Ala541Gly)not specified [RCV004898382]uncertain significance203877161438771614Humanname
598202472CV3946611single nucleotide variantNM_024855.4(ACTR5):c.1732C>T (p.Arg578Cys)not specified [RCV005314465]uncertain significance203877172438771724Humanname
598212273CV3946626single nucleotide variantNM_024855.4(ACTR5):c.1277C>T (p.Pro426Leu)not specified [RCV005316144]uncertain significance203876550238765502Humanname