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Variants search result for Homo sapiens
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52 records found for search term Anxa7
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405710559CV3225787single nucleotide variantNM_001156.5(ANXA7):c.1089+1G>Tnot provided [RCV003990845]likely pathogenic107338003073380030Humanname
8652269CV128844single nucleotide variantNM_001156.3(ANXA7):c.634-495G>ALung cancer [RCV000109331]uncertain significance107338418573384185Humanname
156331129CV2218115single nucleotide variantNM_001156.5(ANXA7):c.435+429C>Tnot specified [RCV004086544]uncertain significance107339609073396090Humanname
597652254CV3555361single nucleotide variantNM_001156.5(ANXA7):c.435+459T>Cnot specified [RCV004833804]uncertain significance107339606073396060Humanname
598229608CV3982967single nucleotide variantNM_001156.5(ANXA7):c.435+452G>Anot specified [RCV005381054]uncertain significance107339606773396067Humanname
155919830CV2209733single nucleotide variantNM_001156.5(ANXA7):c.22C>T (p.Pro8Ser)not specified [RCV004083054]uncertain significance107340083573400835Humanname
156074769CV2321718single nucleotide variantNM_001156.5(ANXA7):c.26C>A (p.Thr9Lys)not specified [RCV004179716]uncertain significance107340083173400831Humanname
401761168CV2726665single nucleotide variantNM_001156.5(ANXA7):c.95A>G (p.Tyr32Cys)not specified [RCV004323008]uncertain significance107339834573398345Humanname
407497227CV3451444single nucleotide variantNM_001156.5(ANXA7):c.58G>T (p.Ala20Ser)not specified [RCV004643694]uncertain significance107339838273398382Humanname
598229866CV3983023single nucleotide variantNM_001156.5(ANXA7):c.64C>A (p.Gln22Lys)not specified [RCV005381095]uncertain significance107339837673398376Humanname
598229909CV3983033single nucleotide variantNM_001156.5(ANXA7):c.35C>T (p.Pro12Leu)not specified [RCV005381102]uncertain significance107340082273400822Humanname
156063720CV2240174single nucleotide variantNM_001156.5(ANXA7):c.268G>C (p.Gly90Arg)not specified [RCV004110932]uncertain significance107339726673397266Humanname
401737612CV2718150single nucleotide variantNM_001156.5(ANXA7):c.133G>A (p.Ala45Thr)not specified [RCV004315857]uncertain significance107339830773398307Humanname
401865713CV2755610single nucleotide variantNM_001156.5(ANXA7):c.185C>T (p.Ala62Val)not specified [RCV004341999]uncertain significance107339825573398255Humanname
407497284CV3451476single nucleotide variantNM_001156.5(ANXA7):c.296G>A (p.Gly99Glu)not specified [RCV004643708]uncertain significance107339723873397238Humanname
407508647CV3458514single nucleotide variantNM_001156.5(ANXA7):c.154A>C (p.Ser52Arg)not specified [RCV004647185]uncertain significance107339828673398286Humanname
597652337CV3555370single nucleotide variantNM_001156.5(ANXA7):c.253C>T (p.Pro85Ser)not specified [RCV004833813]uncertain significance107339818773398187Humanname
598229820CV3983015single nucleotide variantNM_001156.5(ANXA7):c.173G>A (p.Gly58Glu)not specified [RCV005381088]uncertain significance107339826773398267Humanname
15135192CV752260single nucleotide variantNM_001156.5(ANXA7):c.1011C>T (p.Thr337=)not provided [RCV000920808]likely benign107338010973380109Humanname
155925382CV2211821single nucleotide variantNM_001156.5(ANXA7):c.765A>T (p.Glu255Asp)not specified [RCV004086648]uncertain significance107338332873383328Humanname
155998717CV2287186single nucleotide variantNM_001156.5(ANXA7):c.672T>G (p.Asn224Lys)not specified [RCV004146837]uncertain significance107338365273383652Humanname
156089278CV2359357single nucleotide variantNM_001156.5(ANXA7):c.767G>A (p.Arg256His)not specified [RCV004212636]uncertain significance107338332673383326Humanname
156155716CV2393325single nucleotide variantNM_001156.5(ANXA7):c.766C>T (p.Arg256Cys)not specified [RCV004228832]uncertain significance107338332773383327Humanname
329388666CV2469460single nucleotide variantNM_001156.5(ANXA7):c.869G>A (p.Arg290Lys)not specified [RCV004282917]uncertain significance107338322473383224Humanname
401745089CV2681187single nucleotide variantNM_001156.5(ANXA7):c.436C>T (p.Pro146Ser)not specified [RCV004289329]uncertain significance107338841473388414Humanname
401766416CV2732303single nucleotide variantNM_001156.5(ANXA7):c.528G>A (p.Met176Ile)not specified [RCV004331488]uncertain significance107338832273388322Humanname
405696759CV3278852single nucleotide variantNM_001156.5(ANXA7):c.490G>A (p.Asp164Asn)not specified [RCV004424673]uncertain significance107338836073388360Humanname
405696768CV3278853single nucleotide variantNM_001156.5(ANXA7):c.728G>A (p.Ser243Asn)not specified [RCV004424674]uncertain significance107338359673383596Humanname
405696775CV3278854single nucleotide variantNM_001156.5(ANXA7):c.814G>A (p.Glu272Lys)not specified [RCV004424675]uncertain significance107338327973383279Humanname
407508590CV3451454single nucleotide variantNM_001156.5(ANXA7):c.911T>C (p.Met304Thr)not specified [RCV004647167]uncertain significance107338318273383182Humanname
407497252CV3451464single nucleotide variantNM_001156.5(ANXA7):c.496A>G (p.Ile166Val)not specified [RCV004643700]uncertain significance107338835473388354Humanname
407497309CV3458524single nucleotide variantNM_001156.5(ANXA7):c.556A>G (p.Ile186Val)not specified [RCV004643715]uncertain significance107338776673387766Humanname
597652047CV3555335single nucleotide variantNM_001156.5(ANXA7):c.841T>A (p.Phe281Ile)not specified [RCV004833781]uncertain significance107338325273383252Humanname
597652120CV3555344single nucleotide variantNM_001156.5(ANXA7):c.478G>A (p.Ala160Thr)not specified [RCV004833789]uncertain significance107338837273388372Humanname
597652408CV3555378single nucleotide variantNM_001156.5(ANXA7):c.731T>C (p.Leu244Ser)not specified [RCV004833821]uncertain significance107338359373383593Humanname
597652587CV3555398single nucleotide variantNM_001156.5(ANXA7):c.896G>A (p.Arg299His)not specified [RCV004833841]uncertain significance107338319773383197Humanname
597652670CV3555408single nucleotide variantNM_001156.5(ANXA7):c.577C>T (p.Arg193Cys)not specified [RCV004833851]uncertain significance107338774573387745Humanname
598229671CV3982984single nucleotide variantNM_001156.5(ANXA7):c.660G>C (p.Glu220Asp)not specified [RCV005381064]uncertain significance107338366473383664Humanname
598229722CV3982994single nucleotide variantNM_001156.5(ANXA7):c.598A>G (p.Lys200Glu)not specified [RCV005381072]uncertain significance107338772473387724Humanname
153001875CV1682720single nucleotide variantNM_001156.5(ANXA7):c.1055C>T (p.Pro352Leu)not provided [RCV002251799]uncertain significance107338006573380065Humanname
156087603CV2205813single nucleotide variantNM_001156.5(ANXA7):c.1184G>A (p.Arg395His)not specified [RCV004075856]uncertain significance107337900573379005Humanname
156225207CV2219544single nucleotide variantNM_001156.5(ANXA7):c.1087A>G (p.Arg363Gly)not specified [RCV004095280]uncertain significance107338003373380033Humanname
156070294CV2337670single nucleotide variantNM_001156.5(ANXA7):c.1339A>G (p.Met447Val)not specified [RCV004183701]uncertain significance107337615773376157Humanname
155921492CV2350675single nucleotide variantNM_001156.5(ANXA7):c.1100G>A (p.Arg367Gln)not specified [RCV004207024]uncertain significance107337994473379944Humanname
329361730CV2437864single nucleotide variantNM_001156.5(ANXA7):c.1123C>T (p.Arg375Cys)not specified [RCV004261153]uncertain significance107337992173379921Humanname
401776483CV2703246single nucleotide variantNM_001156.5(ANXA7):c.1099C>G (p.Arg367Gly)not specified [RCV004315612]uncertain significance107337994573379945Humanname
401750046CV2704921single nucleotide variantNM_001156.5(ANXA7):c.1255C>T (p.Arg419Trp)not specified [RCV004307492]uncertain significance107337893473378934Humanname
401887816CV2768777single nucleotide variantNM_001156.5(ANXA7):c.1148G>A (p.Ser383Asn)not specified [RCV004346914]uncertain significance107337989673379896Humanname
405696746CV3278850single nucleotide variantNM_001156.5(ANXA7):c.1309G>A (p.Ala437Thr)not specified [RCV004424671]likely benign107337618773376187Humanname
405696754CV3278851single nucleotide variantNM_001156.5(ANXA7):c.1336A>T (p.Thr446Ser)not specified [RCV004424672]uncertain significance107337616073376160Humanname
597652486CV3555387single nucleotide variantNM_001156.5(ANXA7):c.1054C>T (p.Pro352Ser)not specified [RCV004833830]uncertain significance107338006673380066Humanname
15193787CV724062single nucleotide variantNM_001156.5(ANXA7):c.1363G>C (p.Asp455His)not provided [RCV000889042]likely benign107337613373376133Humanname