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Variants search result for Homo sapiens
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80 records found for search term Stim2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597747317CV3618609single nucleotide variantNM_020860.4(STIM2):c.23T>C (p.Val8Ala)not specified [RCV004866042]uncertain significance42686124126861241Humanname
156198952CV2237493single nucleotide variantNM_020860.4(STIM2):c.43T>C (p.Cys15Arg)not specified [RCV004106449]uncertain significance42686126126861261Humanname
156198458CV2255902single nucleotide variantNM_020860.4(STIM2):c.61C>A (p.His21Asn)not specified [RCV004122362]uncertain significance42686127926861279Humanname
156202976CV2300687single nucleotide variantNM_020860.4(STIM2):c.95C>T (p.Ala32Val)not specified [RCV004155628]uncertain significance42686131326861313Humanname
156350371CV2316194single nucleotide variantNM_020860.4(STIM2):c.64C>T (p.Leu22Phe)not specified [RCV004174236]uncertain significance42686128226861282Humanname
156017094CV2370039single nucleotide variantNM_020860.4(STIM2):c.68G>A (p.Arg23His)not specified [RCV004210936]uncertain significance42686128626861286Humanname
401783746CV2723906single nucleotide variantNM_020860.4(STIM2):c.56C>G (p.Pro19Arg)not specified [RCV004326035]uncertain significance42686127426861274Humanname
405740254CV3334387single nucleotide variantNM_020860.4(STIM2):c.56C>T (p.Pro19Leu)not specified [RCV004465600]uncertain significance42686127426861274Humanname
155994214CV2253669single nucleotide variantNM_020860.4(STIM2):c.211G>A (p.Ala71Thr)not specified [RCV004125342]uncertain significance42691956326919563Humanname
155958479CV2282204single nucleotide variantNM_020860.4(STIM2):c.142C>T (p.Leu48Phe)not specified [RCV004132786]uncertain significance42686136026861360Humanname
156166855CV2315264single nucleotide variantNM_020860.4(STIM2):c.145A>G (p.Met49Val)not specified [RCV004167253]uncertain significance42686136326861363Humanname
401769842CV2718912single nucleotide variantNM_020860.4(STIM2):c.146T>A (p.Met49Lys)not specified [RCV004322512]uncertain significance42686136426861364Humanname
401894791CV2785284single nucleotide variantNM_020860.4(STIM2):c.233A>G (p.Gln78Arg)not specified [RCV004357046]uncertain significance42691958526919585Humanname
401923264CV2822469single nucleotide variantNM_020860.4(STIM2):c.1362G>T (p.Leu454=)not provided [RCV003434994]uncertain significance42700887527008875Humanname
407496186CV3485447single nucleotide variantNM_020860.4(STIM2):c.107C>T (p.Ser36Phe)not specified [RCV004668067]uncertain significance42686132526861325Humanname
597747323CV3618610single nucleotide variantNM_020860.4(STIM2):c.115G>A (p.Ala39Thr)not specified [RCV004866043]uncertain significance42686133326861333Humanname
597703776CV3618625single nucleotide variantNM_020860.4(STIM2):c.149C>G (p.Thr50Arg)not specified [RCV004860228]uncertain significance42686136726861367Humanname
598251372CV3919601single nucleotide variantNM_020860.4(STIM2):c.118G>T (p.Ala40Ser)not specified [RCV005277875]uncertain significance42686133626861336Humanname
598251377CV3919602single nucleotide variantNM_020860.4(STIM2):c.119C>T (p.Ala40Val)not specified [RCV005277876]uncertain significance42686133726861337Humanname
156191768CV2223131single nucleotide variantNM_020860.4(STIM2):c.640T>A (p.Trp214Arg)not specified [RCV004103978]uncertain significance42700223127002231Humanname
156342114CV2226010single nucleotide variantNM_020860.4(STIM2):c.346G>A (p.Asp116Asn)not specified [RCV004105169]uncertain significance42695767526957675Humanname
156048212CV2245049single nucleotide variantNM_020860.4(STIM2):c.905G>A (p.Cys302Tyr)not specified [RCV004104769]uncertain significance42700302827003028Humanname
156088447CV2295512single nucleotide variantNM_020860.4(STIM2):c.497C>T (p.Thr166Met)not specified [RCV004160618]uncertain significance42699547826995478Humanname
156174007CV2326901single nucleotide variantNM_020860.4(STIM2):c.863G>A (p.Arg288His)not specified [RCV004176720]uncertain significance42700298627002986Humanname
156086487CV2341027single nucleotide variantNM_020860.4(STIM2):c.542C>A (p.Ser181Tyr)not specified [RCV004181516]uncertain significance42699926426999264Humanname
156133021CV2350237single nucleotide variantNM_020860.4(STIM2):c.707C>T (p.Thr236Met)not specified [RCV004202194]uncertain significance42700229827002298Humanname
155998217CV2373264single nucleotide variantNM_020860.4(STIM2):c.884A>G (p.Asn295Ser)not specified [RCV004217932]uncertain significance42700300727003007Humanname
329357013CV2431221single nucleotide variantNM_020860.4(STIM2):c.892A>G (p.Lys298Glu)not specified [RCV004250563]uncertain significance42700301527003015Humanname
401781200CV2732326single nucleotide variantNM_020860.4(STIM2):c.454C>G (p.Pro152Ala)not specified [RCV004331492]uncertain significance42699543526995435Humanname
401863139CV2776715single nucleotide variantNM_020860.4(STIM2):c.485A>G (p.Asn162Ser)not specified [RCV004357874]uncertain significance42699546626995466Humanname
405740268CV3334389single nucleotide variantNM_020860.4(STIM2):c.907C>T (p.Arg303Trp)not specified [RCV004465602]uncertain significance42700303027003030Humanname
407496193CV3485450single nucleotide variantNM_020860.4(STIM2):c.353A>G (p.His118Arg)not specified [RCV004668069]uncertain significance42695768226957682Humanname
597747332CV3618613single nucleotide variantNM_020860.4(STIM2):c.355A>G (p.Ile119Val)not specified [RCV004866045]uncertain significance42695768426957684Humanname
597703738CV3618620single nucleotide variantNM_020860.4(STIM2):c.346G>T (p.Asp116Tyr)not specified [RCV004860224]uncertain significance42695767526957675Humanname
597703769CV3618623single nucleotide variantNM_020860.4(STIM2):c.655A>T (p.Ile219Phe)not specified [RCV004860227]uncertain significance42700224627002246Humanname
597703786CV3618627single nucleotide variantNM_020860.4(STIM2):c.814G>A (p.Ala272Thr)not specified [RCV004860229]uncertain significance42700293727002937Humanname
597747376CV3618628single nucleotide variantNM_020860.4(STIM2):c.628C>A (p.Pro210Thr)not specified [RCV004866053]uncertain significance42700221927002219Humanname
156135011CV2213279single nucleotide variantNM_020860.4(STIM2):c.1540C>T (p.Arg514Cys)not specified [RCV004085496]uncertain significance42701776127017761Humanname
156400996CV2213709single nucleotide variantNM_020860.4(STIM2):c.1628A>C (p.His543Pro)not specified [RCV004089782]uncertain significance42701784927017849Humanname
156280285CV2224120single nucleotide variantNM_020860.4(STIM2):c.1625G>A (p.Arg542Gln)not specified [RCV004095980]uncertain significance42701784627017846Humanname
156070897CV2232537single nucleotide variantNM_020860.4(STIM2):c.1031G>A (p.Ser344Asn)not specified [RCV004099135]uncertain significance42700758227007582Humanname
156168583CV2237321single nucleotide variantNM_020860.4(STIM2):c.2234C>G (p.Ser745Cys)not specified [RCV004115037]uncertain significance42702298927022989Humanname
156087809CV2241354single nucleotide variantNM_020860.4(STIM2):c.1603G>T (p.Ala535Ser)not specified [RCV004102488]uncertain significance42701782427017824Humanname
156363110CV2330543single nucleotide variantNM_020860.4(STIM2):c.1547G>A (p.Arg516His)not specified [RCV004181107]uncertain significance42701776827017768Humanname
156219298CV2344878single nucleotide variantNM_020860.4(STIM2):c.1796C>T (p.Ser599Phe)not specified [RCV004191017]uncertain significance42702255127022551Humanname
156142672CV2358514single nucleotide variantNM_020860.4(STIM2):c.1970C>T (p.Thr657Ile)not specified [RCV004207398]uncertain significance42702272527022725Humanname
156402139CV2368048single nucleotide variantNM_020860.4(STIM2):c.1613C>T (p.Pro538Leu)not specified [RCV004223130]uncertain significance42701783427017834Humanname
156384363CV2371402single nucleotide variantNM_020860.4(STIM2):c.1667C>T (p.Ser556Phe)not specified [RCV004216669]uncertain significance42701788827017888Humanname
156204736CV2385109single nucleotide variantNM_020860.4(STIM2):c.2080C>T (p.Arg694Cys)not specified [RCV004228371]uncertain significance42702283527022835Humanname
329402634CV2451140single nucleotide variantNM_020860.4(STIM2):c.1561C>T (p.Pro521Ser)not specified [RCV004270073]uncertain significance42701778227017782Humanname
329357011CV2460652single nucleotide variantNM_020860.4(STIM2):c.2081G>T (p.Arg694Leu)not specified [RCV004270702]uncertain significance42702283627022836Humanname
401740772CV2681529single nucleotide variantNM_020860.4(STIM2):c.2209A>G (p.Ile737Val)not specified [RCV004292061]uncertain significance42702296427022964Humanname
401734921CV2690715single nucleotide variantNM_020860.4(STIM2):c.1481A>G (p.Gln494Arg)not specified [RCV004298440]uncertain significance42700899427008994Humanname
401773448CV2698217single nucleotide variantNM_020860.4(STIM2):c.2147G>A (p.Arg716Lys)not specified [RCV004304782]uncertain significance42702290227022902Humanname
401767599CV2727216single nucleotide variantNM_020860.4(STIM2):c.1298G>A (p.Arg433His)not specified [RCV004327346]uncertain significance42700881127008811Humanname
401884661CV2761875single nucleotide variantNM_020860.4(STIM2):c.1100A>G (p.Asn367Ser)not specified [RCV004339514]uncertain significance42700765127007651Humanname
405740234CV3334384single nucleotide variantNM_020860.4(STIM2):c.1712A>T (p.Tyr571Phe)not specified [RCV004465597]uncertain significance42701793327017933Humanname
405740241CV3334385single nucleotide variantNM_020860.4(STIM2):c.1813G>A (p.Gly605Arg)not specified [RCV004465598]uncertain significance42702256827022568Humanname
405740248CV3334386single nucleotide variantNM_020860.4(STIM2):c.1919C>T (p.Ser640Leu)not specified [RCV004465599]uncertain significance42702267427022674Humanname
407496183CV3485445single nucleotide variantNM_020860.4(STIM2):c.1736C>A (p.Ala579Asp)not specified [RCV004668066]uncertain significance42701795727017957Humanname
407530112CV3485446single nucleotide variantNM_020860.4(STIM2):c.1333A>G (p.Ile445Val)not specified [RCV004681653]uncertain significance42700884627008846Humanname
407496190CV3485448single nucleotide variantNM_020860.4(STIM2):c.1367C>T (p.Ser456Phe)not specified [RCV004668068]uncertain significance42700888027008880Humanname
407530113CV3485449single nucleotide variantNM_020860.4(STIM2):c.1251G>C (p.Lys417Asn)not specified [RCV004681654]uncertain significance42700876427008764Humanname
597747312CV3618608single nucleotide variantNM_020860.4(STIM2):c.2015A>G (p.Asn672Ser)not specified [RCV004866041]uncertain significance42702277027022770Humanname
597747328CV3618612single nucleotide variantNM_020860.4(STIM2):c.1954G>A (p.Asp652Asn)not specified [RCV004866044]uncertain significance42702270927022709Humanname
597747338CV3618614single nucleotide variantNM_020860.4(STIM2):c.2189A>G (p.Lys730Arg)not specified [RCV004866046]uncertain significance42702294427022944Humanname
597747344CV3618615single nucleotide variantNM_020860.4(STIM2):c.1231C>T (p.His411Tyr)not specified [RCV004866047]uncertain significance42700850927008509Humanname
597747349CV3618616single nucleotide variantNM_020860.4(STIM2):c.1390T>C (p.Trp464Arg)not specified [RCV004866048]uncertain significance42700890327008903Humanname
597703730CV3618617single nucleotide variantNM_020860.4(STIM2):c.1800A>T (p.Leu600Phe)not specified [RCV004860223]uncertain significance42702255527022555Humanname
597747354CV3618618single nucleotide variantNM_020860.4(STIM2):c.1254A>T (p.Lys418Asn)not specified [RCV004866049]uncertain significance42700876727008767Humanname
597747360CV3618619single nucleotide variantNM_020860.4(STIM2):c.1112A>G (p.Gln371Arg)not specified [RCV004866050]uncertain significance42700766327007663Humanname
597703749CV3618621single nucleotide variantNM_020860.4(STIM2):c.1474G>A (p.Val492Met)not specified [RCV004860225]uncertain significance42700898727008987Humanname
597703759CV3618622single nucleotide variantNM_020860.4(STIM2):c.1082T>C (p.Val361Ala)not specified [RCV004860226]uncertain significance42700763327007633Humanname
597747365CV3618624single nucleotide variantNM_020860.4(STIM2):c.1861T>C (p.Ser621Pro)not specified [RCV004866051]uncertain significance42702261627022616Humanname
597747370CV3618626single nucleotide variantNM_020860.4(STIM2):c.2072C>G (p.Pro691Arg)not specified [RCV004866052]uncertain significance42702282727022827Humanname
597747381CV3618629single nucleotide variantNM_020860.4(STIM2):c.1706C>T (p.Ala569Val)not specified [RCV004866054]uncertain significance42701792727017927Humanname
597747388CV3618630single nucleotide variantNM_020860.4(STIM2):c.1933G>C (p.Asp645His)not specified [RCV004866055]uncertain significance42702268827022688Humanname
598251362CV3919599single nucleotide variantNM_020860.4(STIM2):c.1471A>G (p.Ile491Val)not specified [RCV005277873]uncertain significance42700898427008984Humanname
598251367CV3919600single nucleotide variantNM_020860.4(STIM2):c.1637A>G (p.His546Arg)not specified [RCV005277874]uncertain significance42701785827017858Humanname
8625776CV80900single nucleotide variantNM_001169117.1(STIM2):c.537G>A (p.Met179Ile)Malignant melanoma [RCV000060977]not provided42699925926999259Humanname