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51 records found for search term Sntb2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156398059CV2204141single nucleotide variantNM_006750.4(SNTB2):c.20C>T (p.Thr7Ile)not specified [RCV004076947]uncertain significance166918718669187186Humanname
401768128CV2735185single nucleotide variantNM_006750.4(SNTB2):c.16G>C (p.Ala6Pro)not specified [RCV004333880]uncertain significance166918718269187182Humanname
405731900CV3326320single nucleotide variantNM_006750.4(SNTB2):c.23C>T (p.Ala8Val)not specified [RCV004464444]uncertain significance166918718969187189Humanname
597740902CV3607171single nucleotide variantNM_006750.4(SNTB2):c.19A>G (p.Thr7Ala)not specified [RCV004864751]uncertain significance166918718569187185Humanname
401899677CV2758048single nucleotide variantNM_006750.4(SNTB2):c.57G>C (p.Trp19Cys)not specified [RCV004339214]uncertain significance166918722369187223Humanname
405731946CV3326326single nucleotide variantNM_006750.4(SNTB2):c.65C>T (p.Ala22Val)not specified [RCV004464450]uncertain significance166918723169187231Humanname
597745058CV3607174single nucleotide variantNM_006750.4(SNTB2):c.59C>T (p.Thr20Met)not specified [RCV004865594]uncertain significance166918722569187225Humanname
156271898CV2237293single nucleotide variantNM_006750.4(SNTB2):c.283A>C (p.Ser95Arg)not specified [RCV004115013]uncertain significance166918744969187449Humanname
155930041CV2389296single nucleotide variantNM_006750.4(SNTB2):c.272T>G (p.Leu91Arg)not specified [RCV004235610]uncertain significance166918743869187438Humanname
401883707CV2764492single nucleotide variantNM_006750.4(SNTB2):c.229G>T (p.Gly77Cys)not specified [RCV004339053]uncertain significance166918739569187395Humanname
405731892CV3326319single nucleotide variantNM_006750.4(SNTB2):c.221C>T (p.Pro74Leu)not specified [RCV004464443]uncertain significance166918738769187387Humanname
405731908CV3326321single nucleotide variantNM_006750.4(SNTB2):c.286C>T (p.Pro96Ser)not specified [RCV004464445]uncertain significance166918745269187452Humanname
405731915CV3326322single nucleotide variantNM_006750.4(SNTB2):c.296C>T (p.Pro99Leu)not specified [RCV004464446]uncertain significance166918746269187462Humanname
156034389CV2246470single nucleotide variantNM_006750.4(SNTB2):c.708C>A (p.His236Gln)not specified [RCV004110232]uncertain significance166924572969245729Humanname
156000789CV2287427single nucleotide variantNM_006750.4(SNTB2):c.964G>A (p.Gly322Ser)not specified [RCV004147026]uncertain significance166926021969260219Humanname
156194332CV2322098single nucleotide variantNM_006750.4(SNTB2):c.842G>A (p.Arg281His)not specified [RCV004173840]uncertain significance166926009769260097Humanname
329369037CV2424653single nucleotide variantNM_006750.4(SNTB2):c.698C>T (p.Ser233Leu)not specified [RCV004254523]uncertain significance166924571969245719Humanname
401782298CV2686663single nucleotide variantNM_006750.4(SNTB2):c.614A>C (p.Lys205Thr)not specified [RCV004300075]uncertain significance166924563569245635Humanname
401754175CV2717034single nucleotide variantNM_006750.4(SNTB2):c.877G>A (p.Val293Ile)not specified [RCV004330076]uncertain significance166926013269260132Humanname
401877147CV2790065single nucleotide variantNM_006750.4(SNTB2):c.658C>A (p.Pro220Thr)not specified [RCV004364015]uncertain significance166924567969245679Humanname
405731924CV3326323single nucleotide variantNM_006750.4(SNTB2):c.313G>A (p.Gly105Ser)not specified [RCV004464447]uncertain significance166918747969187479Humanname
405731931CV3326324single nucleotide variantNM_006750.4(SNTB2):c.370G>A (p.Gly124Ser)not specified [RCV004464448]uncertain significance166918753669187536Humanname
405731938CV3326325single nucleotide variantNM_006750.4(SNTB2):c.557C>T (p.Ala186Val)not specified [RCV004464449]uncertain significance166918772369187723Humanname
407503727CV3474672single nucleotide variantNM_006750.4(SNTB2):c.889A>G (p.Thr297Ala)not specified [RCV004670351]uncertain significance166926014469260144Humanname
407503732CV3474674single nucleotide variantNM_006750.4(SNTB2):c.617A>G (p.Lys206Arg)not specified [RCV004670352]uncertain significance166924563869245638Humanname
597745052CV3607173single nucleotide variantNM_006750.4(SNTB2):c.302G>A (p.Arg101Gln)not specified [RCV004865593]uncertain significance166918746869187468Humanname
597745067CV3607178single nucleotide variantNM_006750.4(SNTB2):c.416C>T (p.Pro139Leu)not specified [RCV004865596]uncertain significance166918758269187582Humanname
597740916CV3607180single nucleotide variantNM_006750.4(SNTB2):c.421C>G (p.Leu141Val)not specified [RCV004864754]uncertain significance166918758769187587Humanname
597740920CV3607181single nucleotide variantNM_006750.4(SNTB2):c.695G>C (p.Gly232Ala)not specified [RCV004864755]uncertain significance166924571669245716Humanname
597745077CV3607182single nucleotide variantNM_006750.4(SNTB2):c.313G>T (p.Gly105Cys)not specified [RCV004865598]uncertain significance166918747969187479Humanname
598171550CV3911624single nucleotide variantNM_006750.4(SNTB2):c.968G>T (p.Ser323Ile)not specified [RCV005284861]uncertain significance166926022369260223Humanname
598171556CV3911625single nucleotide variantNM_006750.4(SNTB2):c.677G>A (p.Ser226Asn)not specified [RCV005284862]uncertain significance166924569869245698Humanname
598171568CV3911627single nucleotide variantNM_006750.4(SNTB2):c.974A>T (p.Glu325Val)not specified [RCV005284864]uncertain significance166926022969260229Humanname
598171580CV3911629single nucleotide variantNM_006750.4(SNTB2):c.320C>A (p.Ala107Glu)not specified [RCV005284866]uncertain significance166918748669187486Humanname
156376826CV2206862single nucleotide variantNM_006750.4(SNTB2):c.1595A>G (p.Lys532Arg)not specified [RCV004083534]uncertain significance166930089669300896Humanname
156066897CV2317883single nucleotide variantNM_006750.4(SNTB2):c.1193C>G (p.Ser398Cys)not specified [RCV004175113]uncertain significance166928409269284092Humanname
156225401CV2352655single nucleotide variantNM_006750.4(SNTB2):c.1322A>T (p.Glu441Val)not specified [RCV004198686]uncertain significance166928422169284221Humanname
156187641CV2378090single nucleotide variantNM_006750.4(SNTB2):c.1604G>A (p.Arg535His)not specified [RCV004232648]uncertain significance166930090569300905Humanname
401757817CV2685566single nucleotide variantNM_006750.4(SNTB2):c.1267C>T (p.Arg423Trp)not specified [RCV004294577]uncertain significance166928416669284166Humanname
405731876CV3326317single nucleotide variantNM_006750.4(SNTB2):c.1559C>T (p.Pro520Leu)not specified [RCV004464441]uncertain significance166930086069300860Humanname
405731883CV3326318single nucleotide variantNM_006750.4(SNTB2):c.1592C>T (p.Ala531Val)not specified [RCV004464442]uncertain significance166930089369300893Humanname
407525296CV3474673single nucleotide variantNM_006750.4(SNTB2):c.1226G>A (p.Arg409Gln)not specified [RCV004679118]uncertain significance166928412569284125Humanname
597740897CV3607170single nucleotide variantNM_006750.4(SNTB2):c.1445G>A (p.Arg482His)not specified [RCV004864750]uncertain significance166929968969299689Humanname
597745047CV3607172single nucleotide variantNM_006750.4(SNTB2):c.1175G>A (p.Arg392Gln)not specified [RCV004865592]uncertain significance166928407469284074Humanname
597740907CV3607175single nucleotide variantNM_006750.4(SNTB2):c.1003C>G (p.Gln335Glu)not specified [RCV004864752]uncertain significance166926025869260258Humanname
597740912CV3607176single nucleotide variantNM_006750.4(SNTB2):c.1129T>C (p.Tyr377His)not specified [RCV004864753]uncertain significance166927026669270266Humanname
597745061CV3607177single nucleotide variantNM_006750.4(SNTB2):c.1468A>T (p.Met490Leu)not specified [RCV004865595]uncertain significance166929971269299712Humanname
597745072CV3607179single nucleotide variantNM_006750.4(SNTB2):c.1595A>T (p.Lys532Ile)not specified [RCV004865597]uncertain significance166930089669300896Humanname
598171544CV3911623single nucleotide variantNM_006750.4(SNTB2):c.1589C>T (p.Ser530Leu)not specified [RCV005284860]uncertain significance166930089069300890Humanname
598171562CV3911626single nucleotide variantNM_006750.4(SNTB2):c.1519G>A (p.Glu507Lys)not specified [RCV005284863]uncertain significance166929976369299763Humanname
598171575CV3911628single nucleotide variantNM_006750.4(SNTB2):c.1293A>G (p.Ile431Met)not specified [RCV005284865]uncertain significance166928419269284192Humanname