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Variants search result for Homo sapiens
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49 records found for search term Tssc4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156397340CV2200326single nucleotide variantNM_005706.4(TSSC4):c.79G>A (p.Asp27Asn)not specified [RCV004076658]uncertain significance1124027122402712Humanname
156255407CV2359015single nucleotide variantNM_005706.4(TSSC4):c.56C>T (p.Thr19Met)not specified [RCV004212340]uncertain significance1124026892402689Humanname
405799233CV3341022single nucleotide variantNM_005706.4(TSSC4):c.68C>T (p.Thr23Met)not specified [RCV004476767]uncertain significance1124027012402701Humanname
15198867CV701709single nucleotide variantNM_005706.4(TSSC4):c.864C>T (p.Val288=)not provided [RCV000956881]benign1124034972403497Humanname
156048224CV2271707single nucleotide variantNM_005706.4(TSSC4):c.135A>C (p.Glu45Asp)not specified [RCV004130554]uncertain significance1124027682402768Humanname
401782531CV2686908single nucleotide variantNM_005706.4(TSSC4):c.194C>T (p.Pro65Leu)not specified [RCV004302080]uncertain significance1124028272402827Humanname
401747338CV2698845single nucleotide variantNM_005706.4(TSSC4):c.115A>G (p.Ser39Gly)not specified [RCV004301282]uncertain significance1124027482402748Humanname
405799215CV3341016single nucleotide variantNM_005706.4(TSSC4):c.190G>A (p.Glu64Lys)not specified [RCV004476761]uncertain significance1124028232402823Humanname
405799221CV3341018single nucleotide variantNM_005706.4(TSSC4):c.267C>G (p.Phe89Leu)not specified [RCV004476763]uncertain significance1124029002402900Humanname
407528687CV3487104single nucleotide variantNM_005706.4(TSSC4):c.274C>T (p.Arg92Cys)not specified [RCV004680513]uncertain significance1124029072402907Humanname
597788674CV3618174single nucleotide variantNM_005706.4(TSSC4):c.221C>T (p.Pro74Leu)not specified [RCV004875916]uncertain significance1124028542402854Humanname
598216958CV3925005single nucleotide variantNM_005706.4(TSSC4):c.136G>A (p.Val46Met)not specified [RCV005292954]uncertain significance1124027692402769Humanname
598238676CV3925007single nucleotide variantNM_005706.4(TSSC4):c.242A>T (p.His81Leu)not specified [RCV005296454]uncertain significance1124028752402875Humanname
598216980CV3925010single nucleotide variantNM_005706.4(TSSC4):c.268T>A (p.Ser90Thr)not specified [RCV005292957]uncertain significance1124029012402901Humanname
598216988CV3925012single nucleotide variantNM_005706.4(TSSC4):c.112C>G (p.Leu38Val)not specified [RCV005292958]uncertain significance1124027452402745Humanname
156370775CV2204324single nucleotide variantNM_005706.4(TSSC4):c.916G>A (p.Gly306Ser)not specified [RCV004079148]uncertain significance1124035492403549Humanname
155920427CV2210805single nucleotide variantNM_005706.4(TSSC4):c.452C>T (p.Pro151Leu)not specified [RCV004085897]uncertain significance1124030852403085Humanname
155946153CV2238082single nucleotide variantNM_005706.4(TSSC4):c.350G>A (p.Ser117Asn)not specified [RCV004111102]uncertain significance1124029832402983Humanname
156236596CV2239034single nucleotide variantNM_005706.4(TSSC4):c.914A>G (p.His305Arg)not specified [RCV004109912]uncertain significance1124035472403547Humanname
156181783CV2255132single nucleotide variantNM_005706.4(TSSC4):c.392G>A (p.Arg131Gln)not specified [RCV004115758]likely benign1124030252403025Humanname
156203507CV2334953single nucleotide variantNM_005706.4(TSSC4):c.592G>A (p.Val198Met)not specified [RCV004599560]uncertain significance1124032252403225Humanname
156051762CV2336686single nucleotide variantNM_005706.4(TSSC4):c.317G>A (p.Arg106Gln)not specified [RCV004196926]likely benign1124029502402950Humanname
156347628CV2375515single nucleotide variantNM_005706.4(TSSC4):c.946C>G (p.Arg316Gly)not specified [RCV004226024]uncertain significance1124035792403579Humanname
155905444CV2393061single nucleotide variantNM_005706.4(TSSC4):c.613C>T (p.Pro205Ser)not specified [RCV004226550]uncertain significance1124032462403246Humanname
156220652CV2397316single nucleotide variantNM_005706.4(TSSC4):c.724G>A (p.Gly242Ser)not specified [RCV004238843]uncertain significance1124033572403357Humanname
329355075CV2448989single nucleotide variantNM_005706.4(TSSC4):c.659G>A (p.Arg220Gln)not specified [RCV004264071]uncertain significance1124032922403292Humanname
401727944CV2675874single nucleotide variantNM_005706.4(TSSC4):c.868A>G (p.Ser290Gly)not specified [RCV004281878]uncertain significance1124035012403501Humanname
401722837CV2677114single nucleotide variantNM_005706.4(TSSC4):c.514G>A (p.Glu172Lys)not specified [RCV004295751]uncertain significance1124031472403147Humanname
401725831CV2687292single nucleotide variantNM_005706.4(TSSC4):c.481C>T (p.Arg161Cys)not specified [RCV004298226]uncertain significance1124031142403114Humanname
401726336CV2695649single nucleotide variantNM_005706.4(TSSC4):c.517G>C (p.Val173Leu)not specified [RCV004299462]uncertain significance1124031502403150Humanname
401720704CV2702065single nucleotide variantNM_005706.4(TSSC4):c.946C>T (p.Arg316Trp)not specified [RCV004320642]uncertain significance1124035792403579Humanname
401768799CV2735435single nucleotide variantNM_005706.4(TSSC4):c.596C>T (p.Ser199Phe)not specified [RCV004330997]uncertain significance1124032292403229Humanname
405799224CV3341019single nucleotide variantNM_005706.4(TSSC4):c.535C>G (p.Gln179Glu)not specified [RCV004476764]uncertain significance1124031682403168Humanname
405799227CV3341020single nucleotide variantNM_005706.4(TSSC4):c.569G>T (p.Ser190Ile)not specified [RCV004476765]uncertain significance1124032022403202Humanname
405799236CV3341023single nucleotide variantNM_005706.4(TSSC4):c.790G>A (p.Gly264Arg)not specified [RCV004476768]uncertain significance1124034232403423Humanname
405799239CV3341024single nucleotide variantNM_005706.4(TSSC4):c.812G>C (p.Trp271Ser)not specified [RCV004476769]uncertain significance1124034452403445Humanname
405799242CV3341025single nucleotide variantNM_005706.4(TSSC4):c.898G>C (p.Glu300Gln)not specified [RCV004476770]uncertain significance1124035312403531Humanname
405799245CV3341026single nucleotide variantNM_005706.4(TSSC4):c.929G>A (p.Arg310Gln)not specified [RCV004476771]uncertain significance1124035622403562Humanname
405799248CV3341027single nucleotide variantNM_005706.4(TSSC4):c.947G>A (p.Arg316Gln)not specified [RCV004476772]uncertain significance1124035802403580Humanname
597788660CV3618171single nucleotide variantNM_005706.4(TSSC4):c.521G>A (p.Ser174Asn)not specified [RCV004875913]uncertain significance1124031542403154Humanname
597788664CV3618172single nucleotide variantNM_005706.4(TSSC4):c.886C>A (p.Leu296Ile)not specified [RCV004875914]uncertain significance1124035192403519Humanname
597788668CV3618173single nucleotide variantNM_005706.4(TSSC4):c.533A>G (p.Asn178Ser)not specified [RCV004875915]uncertain significance1124031662403166Humanname
597788678CV3618175single nucleotide variantNM_005706.4(TSSC4):c.348G>A (p.Met116Ile)not specified [RCV004875917]uncertain significance1124029812402981Humanname
598238669CV3925004single nucleotide variantNM_005706.4(TSSC4):c.893C>T (p.Pro298Leu)not specified [RCV005296453]uncertain significance1124035262403526Humanname
598216965CV3925006single nucleotide variantNM_005706.4(TSSC4):c.341C>T (p.Thr114Ile)not specified [RCV005292955]uncertain significance1124029742402974Humanname
598238682CV3925008single nucleotide variantNM_005706.4(TSSC4):c.788C>T (p.Pro263Leu)not specified [RCV005296455]uncertain significance1124034212403421Humanname
598216973CV3925009single nucleotide variantNM_005706.4(TSSC4):c.415A>G (p.Arg139Gly)not specified [RCV005292956]likely benign1124030482403048Humanname
598252636CV3925013single nucleotide variantNM_005706.4(TSSC4):c.428G>T (p.Ser143Ile)not specified [RCV005298931]uncertain significance1124030612403061Humanname
15159624CV701708single nucleotide variantNM_005706.4(TSSC4):c.371G>A (p.Arg124Gln)not provided [RCV000947313]benign1124030042403004Humanname