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51 records found for search term Elmo1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15187077CV744341single nucleotide variantNM_014800.11(ELMO1):c.780+8G>Cnot provided [RCV000908990]benign73722260737222607Humanname
8590784CV125493single nucleotide variantNM_001039459.2(ELMO1):c.-4+6726C>ALung cancer [RCV000106012]uncertain significance73697818936978189Humanname
8590786CV125495single nucleotide variantNM_001206480.2(ELMO1):c.192+6197T>CLung cancer [RCV000106014]uncertain significance73730865337308653Humanname
8590787CV125496single nucleotide variantNM_001206480.2(ELMO1):c.-73-41533G>TLung cancer [RCV000106015]uncertain significance73738429637384296Humanname
8590788CV125497single nucleotide variantNM_001206480.2(ELMO1):c.-73-50934A>TLung cancer [RCV000106016]uncertain significance73739369737393697Humanname
8590789CV125498single nucleotide variantNM_001206480.2(ELMO1):c.-74+42054T>CLung cancer [RCV000106017]uncertain significance73740680637406806Humanname
8590790CV125499single nucleotide variantNM_001206480.2(ELMO1):c.-74+31823C>GLung cancer [RCV000106018]uncertain significance73741703737417037Humanname
329402244CV2454086single nucleotide variantNM_014800.11(ELMO1):c.65T>C (p.Met22Thr)not specified [RCV004265592]uncertain significance73734262637342626Humanname
329378794CV2459955single nucleotide variantNM_014800.11(ELMO1):c.275T>C (p.Ile92Thr)not specified [RCV004279438]uncertain significance73725931937259319Humanname
597746970CV3670959single nucleotide variantNM_014800.11(ELMO1):c.172A>T (p.Asn58Tyr)not specified [RCV004922807]uncertain significance73731487037314870Humanname
598191014CV3957758single nucleotide variantNM_014800.11(ELMO1):c.296C>T (p.Ala99Val)not specified [RCV005334777]uncertain significance73725929837259298Humanname
8626417CV81561single nucleotide variantNM_014800.10(ELMO1):c.295G>A (p.Ala99Thr)Malignant melanoma [RCV000061639]not provided73725929937259299Humanname
156024587CV2242145single nucleotide variantNM_014800.11(ELMO1):c.983G>T (p.Arg328Leu)not specified [RCV004109359]uncertain significance73721148937211489Humanname
156035590CV2282991single nucleotide variantNM_014800.11(ELMO1):c.926T>C (p.Met309Thr)not specified [RCV004143620]uncertain significance73721336337213363Humanname
156181034CV2288138single nucleotide variantNM_014800.11(ELMO1):c.406G>A (p.Gly136Ser)not specified [RCV004149666]uncertain significance73725918837259188Humanname
156192820CV2289465single nucleotide variantNM_014800.11(ELMO1):c.712G>A (p.Glu238Lys)not specified [RCV004152408]uncertain significance73722268337222683Humanname
156350695CV2316253single nucleotide variantNM_014800.11(ELMO1):c.536C>T (p.Ala179Val)not specified [RCV004174284]uncertain significance73723310837233108Humanname
329368584CV2428070single nucleotide variantNM_014800.11(ELMO1):c.532G>A (p.Val178Met)not specified [RCV004254445]uncertain significance73723311237233112Humanname
329376083CV2437964single nucleotide variantNM_014800.11(ELMO1):c.479C>T (p.Thr160Met)not specified [RCV004263681]uncertain significance73723316537233165Humanname
329355970CV2442419single nucleotide variantNM_014800.11(ELMO1):c.815G>T (p.Arg272Leu)not specified [RCV004266667]uncertain significance73721666137216661Humanname
329401662CV2457286single nucleotide variantNM_014800.11(ELMO1):c.503A>G (p.His168Arg)not specified [RCV004267134]uncertain significance73723314137233141Humanname
401891587CV2780556single nucleotide variantNM_014800.11(ELMO1):c.587C>T (p.Ser196Leu)not specified [RCV004351932]uncertain significance73722499337224993Humanname
405051211CV3081665single nucleotide variantNM_014800.11(ELMO1):c.376A>G (p.Ile126Val)not provided [RCV003740622]uncertain significance73725921837259218Humanname
597666415CV3670954single nucleotide variantNM_014800.11(ELMO1):c.523A>T (p.Thr175Ser)not specified [RCV004912549]uncertain significance73723312137233121Humanname
597666421CV3670955single nucleotide variantNM_014800.11(ELMO1):c.731T>C (p.Ile244Thr)not specified [RCV004912550]uncertain significance73722266437222664Humanname
598191038CV3957761single nucleotide variantNM_014800.11(ELMO1):c.389C>T (p.Thr130Met)not specified [RCV005334780]uncertain significance73725920537259205Humanname
598191044CV3957762single nucleotide variantNM_014800.11(ELMO1):c.829A>T (p.Thr277Ser)not specified [RCV005334781]uncertain significance73721664737216647Humanname
598191059CV3957764single nucleotide variantNM_014800.11(ELMO1):c.788C>T (p.Ala263Val)not specified [RCV005334783]uncertain significance73721668837216688Humanname
8632568CV87776single nucleotide variantNM_001206482.1(ELMO1):c.28G>A (p.Val10Met)Malignant melanoma [RCV000067868]not provided73734266337342663Humanname
156272725CV2277567single nucleotide variantNM_014800.11(ELMO1):c.1579G>A (p.Asp527Asn)not specified [RCV004145253]uncertain significance73689487636894876Humanname
156290200CV2309797single nucleotide variantNM_014800.11(ELMO1):c.1825C>T (p.Pro609Ser)not specified [RCV004160916]uncertain significance73687047336870473Humanname
156169543CV2315464single nucleotide variantNM_014800.11(ELMO1):c.1043G>A (p.Arg348His)not specified [RCV004167415]uncertain significance73721142937211429Humanname
155974074CV2317820single nucleotide variantNM_014800.11(ELMO1):c.1105A>G (p.Met369Val)not specified [RCV004175063]uncertain significance73713321637133216Humanname
156202030CV2334633single nucleotide variantNM_014800.11(ELMO1):c.1973A>G (p.Asp658Gly)not specified [RCV004188619]uncertain significance73686166936861669Humanname
155904253CV2353805single nucleotide variantNM_014800.11(ELMO1):c.2116A>G (p.Ile706Val)not specified [RCV004201810]uncertain significance73685561936855619Humanname
155926908CV2365841single nucleotide variantNM_014800.11(ELMO1):c.2048G>A (p.Arg683Gln)not specified [RCV004214375]uncertain significance73685568736855687Humanname
329362350CV2444626single nucleotide variantNM_014800.11(ELMO1):c.1997C>T (p.Thr666Met)not specified [RCV004258895]uncertain significance73685573836855738Humanname
329355549CV2445538single nucleotide variantNM_014800.11(ELMO1):c.1244G>A (p.Arg415His)not specified [RCV004257589]uncertain significance73709667537096675Humanname
405738796CV3248532single nucleotide variantNM_014800.11(ELMO1):c.1442T>C (p.Met481Thr)not specified [RCV004380235]uncertain significance73689501336895013Humanname
405738810CV3248534single nucleotide variantNM_014800.11(ELMO1):c.1597A>G (p.Ile533Val)not specified [RCV004380237]uncertain significance73689485836894858Humanname
407506649CV3438295single nucleotide variantNM_014800.11(ELMO1):c.1324C>T (p.His442Tyr)not specified [RCV004624765]uncertain significance73701341237013412Humanname
407506651CV3438296single nucleotide variantNM_014800.11(ELMO1):c.1478C>A (p.Thr493Lys)not specified [RCV004624766]uncertain significance73689497736894977Humanname
407506653CV3438297single nucleotide variantNM_014800.11(ELMO1):c.1135T>G (p.Leu379Val)not specified [RCV004624767]uncertain significance73713318637133186Humanname
407506656CV3438298single nucleotide variantNM_014800.11(ELMO1):c.1592G>A (p.Arg531His)not specified [RCV004624768]uncertain significance73689486336894863Humanname
597746956CV3670956single nucleotide variantNM_014800.11(ELMO1):c.1318G>A (p.Asp440Asn)not specified [RCV004922804]uncertain significance73701341837013418Humanname
597746961CV3670957single nucleotide variantNM_014800.11(ELMO1):c.2047C>T (p.Arg683Trp)not specified [RCV004922805]uncertain significance73685568836855688Humanname
597746966CV3670958single nucleotide variantNM_014800.11(ELMO1):c.1199T>C (p.Leu400Pro)not specified [RCV004922806]uncertain significance73709672037096720Humanname
598191030CV3957760single nucleotide variantNM_014800.11(ELMO1):c.1697A>G (p.Asn566Ser)not specified [RCV005334779]uncertain significance73688757736887577Humanname
598191051CV3957763single nucleotide variantNM_014800.11(ELMO1):c.1798C>T (p.Pro600Ser)not specified [RCV005334782]uncertain significance73687803436878034Humanname
8626416CV81560single nucleotide variantNM_014800.10(ELMO1):c.1081T>C (p.Phe361Leu)Malignant melanoma [RCV000061638]not provided73721139137211391Humanname
8632567CV87775single nucleotide variantNM_001206482.1(ELMO1):c.939G>A (p.Met313Ile)Malignant melanoma [RCV000067867]not provided73721335037213350Humanname