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Variants search result for Homo sapiens
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47 records found for search term Htr1d
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15174351CV732269single nucleotide variantNM_000864.5(HTR1D):c.126C>T (p.Ala42=)not provided [RCV000905947]benign12319409423194094Humanname
597783012CV3686131single nucleotide variantNM_000864.5(HTR1D):c.29G>A (p.Gly10Asp)not specified [RCV004931308]uncertain significance12319419123194191Humanname
15185932CV696575single nucleotide variantNM_000864.5(HTR1D):c.558G>A (p.Ser186=)not provided [RCV000953131]benign12319366223193662Humanname
156140637CV2212207single nucleotide variantNM_000864.5(HTR1D):c.214C>G (p.Pro72Ala)not specified [RCV004089096]uncertain significance12319400623194006Humanname
405804176CV3270589single nucleotide variantNM_000864.5(HTR1D):c.167A>T (p.Asn56Ile)not specified [RCV004404838]uncertain significance12319405323194053Humanname
8629359CV84504single nucleotide variantNM_000864.4(HTR1D):c.271G>A (p.Val91Ile)Malignant melanoma [RCV000064586]not provided12319394923193949Humanname
155922206CV2218768single nucleotide variantNM_000864.5(HTR1D):c.722C>T (p.Thr241Met)not specified [RCV004085020]uncertain significance12319349823193498Humanname
156381982CV2227142single nucleotide variantNM_000864.5(HTR1D):c.595A>G (p.Ile199Val)not specified [RCV004091759]uncertain significance12319362523193625Humanname
156334084CV2230863single nucleotide variantNM_000864.5(HTR1D):c.454G>T (p.Ala152Ser)not specified [RCV004092343]uncertain significance12319376623193766Humanname
156083834CV2244502single nucleotide variantNM_000864.5(HTR1D):c.503G>T (p.Cys168Phe)not specified [RCV004100458]uncertain significance12319371723193717Humanname
156081965CV2249097single nucleotide variantNM_000864.5(HTR1D):c.887A>C (p.Glu296Ala)not specified [RCV004118157]uncertain significance12319333323193333Humanname
155992214CV2255792single nucleotide variantNM_000864.5(HTR1D):c.700C>G (p.Leu234Val)not specified [RCV004120166]uncertain significance12319352023193520Humanname
156283454CV2291821single nucleotide variantNM_000864.5(HTR1D):c.853G>A (p.Ala285Thr)not specified [RCV004158354]uncertain significance12319336723193367Humanname
156274985CV2351778single nucleotide variantNM_000864.5(HTR1D):c.359C>T (p.Thr120Met)not specified [RCV004197935]uncertain significance12319386123193861Humanname
156003573CV2357472single nucleotide variantNM_000864.5(HTR1D):c.952T>G (p.Phe318Val)not specified [RCV004202760]uncertain significance12319326823193268Humanname
156088771CV2359283single nucleotide variantNM_000864.5(HTR1D):c.622A>G (p.Ile208Val)not specified [RCV004212571]uncertain significance12319359823193598Humanname
156085185CV2366142single nucleotide variantNM_000864.5(HTR1D):c.783T>G (p.His261Gln)not specified [RCV004210174]uncertain significance12319343723193437Humanname
155998929CV2373353single nucleotide variantNM_000864.5(HTR1D):c.452C>T (p.Thr151Met)not specified [RCV004220061]uncertain significance12319376823193768Humanname
155906429CV2379023single nucleotide variantNM_000864.5(HTR1D):c.764C>T (p.Ser255Leu)not specified [RCV004233784]uncertain significance12319345623193456Humanname
156227796CV2388309single nucleotide variantNM_000864.5(HTR1D):c.470C>A (p.Thr157Asn)not specified [RCV004234761]uncertain significance12319375023193750Humanname
156088981CV2392016single nucleotide variantNM_000864.5(HTR1D):c.982C>T (p.Arg328Trp)not specified [RCV004235872]uncertain significance12319323823193238Humanname
329396821CV2468241single nucleotide variantNM_000864.5(HTR1D):c.494T>G (p.Ile165Ser)not specified [RCV004275809]uncertain significance12319372623193726Humanname
401739495CV2684090single nucleotide variantNM_000864.5(HTR1D):c.857T>C (p.Leu286Pro)not specified [RCV004295682]uncertain significance12319336323193363Humanname
401770656CV2685824single nucleotide variantNM_000864.5(HTR1D):c.891G>C (p.Arg297Ser)not specified [RCV004294810]uncertain significance12319332923193329Humanname
401772022CV2689715single nucleotide variantNM_000864.5(HTR1D):c.665G>A (p.Arg222Gln)not specified [RCV004297632]uncertain significance12319355523193555Humanname
401783396CV2723527single nucleotide variantNM_000864.5(HTR1D):c.664C>T (p.Arg222Trp)not specified [RCV004323932]uncertain significance12319355623193556Humanname
401856905CV2755175single nucleotide variantNM_000864.5(HTR1D):c.712C>T (p.Arg238Cys)not specified [RCV004337368]uncertain significance12319350823193508Humanname
405804177CV3270590single nucleotide variantNM_000864.5(HTR1D):c.314A>G (p.Asn105Ser)not specified [RCV004404839]likely benign12319390623193906Humanname
405804179CV3270591single nucleotide variantNM_000864.5(HTR1D):c.679C>T (p.Arg227Cys)not specified [RCV004404840]uncertain significance12319354123193541Humanname
405804181CV3270592single nucleotide variantNM_000864.5(HTR1D):c.736A>C (p.Thr246Pro)not specified [RCV004404841]uncertain significance12319348423193484Humanname
405804419CV3270593single nucleotide variantNM_000864.5(HTR1D):c.799T>C (p.Ser267Pro)not specified [RCV004404842]uncertain significance12319342123193421Humanname
405804417CV3270594single nucleotide variantNM_000864.5(HTR1D):c.833A>C (p.Lys278Thr)not specified [RCV004404843]uncertain significance12319338723193387Humanname
405804415CV3270595single nucleotide variantNM_000864.5(HTR1D):c.867G>T (p.Lys289Asn)not specified [RCV004404844]uncertain significance12319335323193353Humanname
407510931CV3444203single nucleotide variantNM_000864.5(HTR1D):c.478G>A (p.Ala160Thr)not specified [RCV004626296]uncertain significance12319374223193742Humanname
407465212CV3444204single nucleotide variantNM_000864.5(HTR1D):c.682A>T (p.Ile228Phe)not specified [RCV004635306]uncertain significance12319353823193538Humanname
597783002CV3686128single nucleotide variantNM_000864.5(HTR1D):c.557C>T (p.Ser186Leu)not specified [RCV004931305]uncertain significance12319366323193663Humanname
597783004CV3686129single nucleotide variantNM_000864.5(HTR1D):c.518C>T (p.Pro173Leu)not specified [RCV004931306]uncertain significance12319370223193702Humanname
597783008CV3686130single nucleotide variantNM_000864.5(HTR1D):c.470C>T (p.Thr157Ile)not specified [RCV004931307]uncertain significance12319375023193750Humanname
598256429CV3968384single nucleotide variantNM_000864.5(HTR1D):c.650A>G (p.Tyr217Cys)not specified [RCV005346791]uncertain significance12319357023193570Humanname
598205932CV3968385single nucleotide variantNM_000864.5(HTR1D):c.983G>A (p.Arg328Gln)not specified [RCV005337689]uncertain significance12319323723193237Humanname
598256433CV3968386single nucleotide variantNM_000864.5(HTR1D):c.463G>A (p.Ala155Thr)not specified [RCV005346792]uncertain significance12319375723193757Humanname
598256435CV3968387single nucleotide variantNM_000864.5(HTR1D):c.614C>T (p.Ala205Val)not specified [RCV005346793]uncertain significance12319360623193606Humanname
15173593CV707207single nucleotide variantNM_000864.5(HTR1D):c.794C>T (p.Ser265Leu)not provided [RCV000972621]benign12319342623193426Humanname
401741691CV2677416single nucleotide variantNM_000864.5(HTR1D):c.1126G>C (p.Ala376Pro)not specified [RCV004289491]uncertain significance12319309423193094Humanname
405804174CV3270588single nucleotide variantNM_000864.5(HTR1D):c.1091G>A (p.Arg364Gln)not specified [RCV004404837]uncertain significance12319312923193129Humanname
597782994CV3686126single nucleotide variantNM_000864.5(HTR1D):c.1127C>T (p.Ala376Val)not specified [RCV004931303]uncertain significance12319309323193093Humanname
597782998CV3686127single nucleotide variantNM_000864.5(HTR1D):c.1094A>G (p.Gln365Arg)not specified [RCV004931304]uncertain significance12319312623193126Humanname