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Variants search result for Homo sapiens
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52 records found for search term Chst12
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407455947CV3422900single nucleotide variantNM_018641.5(CHST12):c.5C>T (p.Thr2Ile)not specified [RCV004610529]uncertain significance724326442432644Humanname
15122471CV750570single nucleotide variantNM_018641.5(CHST12):c.93C>T (p.Ala31=)not provided [RCV000918652]likely benign724327322432732Humanname
597770804CV3653441single nucleotide variantNM_018641.5(CHST12):c.13C>T (p.Arg5Trp)not specified [RCV004896995]uncertain significance724326522432652Humanname
155920811CV2350569single nucleotide variantNM_018641.5(CHST12):c.37C>G (p.Leu13Val)not specified [RCV004204922]uncertain significance724326762432676Humanname
405867242CV2842768single nucleotide variantNM_018641.5(CHST12):c.936G>A (p.Thr312=)EBV-positive nodal T- and NK-cell lymphoma [RCV004558125]likely benign724335752433575Humanname
156156774CV2266240single nucleotide variantNM_018641.5(CHST12):c.197T>A (p.Val66Asp)not specified [RCV004128804]uncertain significance724328362432836Humanname
156068006CV2317961single nucleotide variantNM_018641.5(CHST12):c.216G>C (p.Lys72Asn)not specified [RCV004177082]uncertain significance724328552432855Humanname
401753760CV2685050single nucleotide variantNM_018641.5(CHST12):c.195T>G (p.Asp65Glu)not specified [RCV004289630]uncertain significance724328342432834Humanname
401771492CV2686198single nucleotide variantNM_018641.5(CHST12):c.263C>T (p.Thr88Met)not specified [RCV004297294]uncertain significance724329022432902Humanname
401893452CV2763432single nucleotide variantNM_018641.5(CHST12):c.161C>T (p.Pro54Leu)not specified [RCV004349321]uncertain significance724328002432800Humanname
401891773CV2780747single nucleotide variantNM_018641.5(CHST12):c.169G>T (p.Asp57Tyr)not specified [RCV004352075]uncertain significance724328082432808Humanname
405672490CV3297387single nucleotide variantNM_018641.5(CHST12):c.182C>G (p.Thr61Arg)not specified [RCV004441568]uncertain significance724328212432821Humanname
405672494CV3297388single nucleotide variantNM_018641.5(CHST12):c.244G>A (p.Asp82Asn)not specified [RCV004441569]uncertain significance724328832432883Humanname
407455945CV3422899single nucleotide variantNM_018641.5(CHST12):c.140C>T (p.Pro47Leu)not specified [RCV004610528]uncertain significance724327792432779Humanname
407455950CV3422901single nucleotide variantNM_018641.5(CHST12):c.289A>G (p.Met97Val)not specified [RCV004610530]uncertain significance724329282432928Humanname
407455955CV3422903single nucleotide variantNM_018641.5(CHST12):c.215A>G (p.Lys72Arg)not specified [RCV004610532]uncertain significance724328542432854Humanname
598215590CV3951809single nucleotide variantNM_018641.5(CHST12):c.261G>C (p.Glu87Asp)not specified [RCV005316786]uncertain significance724329002432900Humanname
156132411CV2206591single nucleotide variantNM_018641.5(CHST12):c.419C>T (p.Pro140Leu)not specified [RCV004080936]uncertain significance724330582433058Humanname
156072673CV2240537single nucleotide variantNM_018641.5(CHST12):c.584C>G (p.Pro195Arg)not specified [RCV004119193]uncertain significance724332232433223Humanname
156079215CV2248548single nucleotide variantNM_018641.5(CHST12):c.299G>C (p.Ser100Thr)not specified [RCV004121460]uncertain significance724329382432938Humanname
156237030CV2268343single nucleotide variantNM_018641.5(CHST12):c.608C>T (p.Pro203Leu)not specified [RCV004138624]uncertain significance724332472433247Humanname
156033164CV2275088single nucleotide variantNM_018641.5(CHST12):c.601C>T (p.Arg201Cys)not specified [RCV004136899]uncertain significance724332402433240Humanname
156107036CV2303874single nucleotide variantNM_018641.5(CHST12):c.938A>G (p.Glu313Gly)not specified [RCV004168162]uncertain significance724335772433577Humanname
155971103CV2335652single nucleotide variantNM_018641.5(CHST12):c.611G>A (p.Arg204His)not specified [RCV004193854]uncertain significance724332502433250Humanname
156090643CV2384509single nucleotide variantNM_018641.5(CHST12):c.902C>A (p.Ala301Asp)not specified [RCV004230301]uncertain significance724335412433541Humanname
156215973CV2386027single nucleotide variantNM_018641.5(CHST12):c.999G>T (p.Gln333His)not specified [RCV004229093]uncertain significance724336382433638Humanname
329394565CV2461414single nucleotide variantNM_018641.5(CHST12):c.992C>T (p.Pro331Leu)not specified [RCV004267564]uncertain significance724336312433631Humanname
401768533CV2675414single nucleotide variantNM_018641.5(CHST12):c.613G>A (p.Glu205Lys)not specified [RCV004292215]uncertain significance724332522433252Humanname
401745944CV2678737single nucleotide variantNM_018641.5(CHST12):c.877C>T (p.Arg293Cys)not specified [RCV004292733]uncertain significance724335162433516Humanname
401733829CV2687359single nucleotide variantNM_018641.5(CHST12):c.661C>T (p.Arg221Cys)not specified [RCV004298288]uncertain significance724333002433300Humanname
401732826CV2705046single nucleotide variantNM_018641.5(CHST12):c.542T>A (p.Val181Glu)not specified [RCV004309964]uncertain significance724331812433181Humanname
401861697CV2756424single nucleotide variantNM_018641.5(CHST12):c.863C>T (p.Ala288Val)not specified [RCV004342961]likely benign724335022433502Humanname
401888081CV2791226single nucleotide variantNM_018641.5(CHST12):c.789C>G (p.Asn263Lys)not specified [RCV004356866]uncertain significance724334282433428Humanname
405672498CV3297389single nucleotide variantNM_018641.5(CHST12):c.323C>T (p.Pro108Leu)not specified [RCV004441570]uncertain significance724329622432962Humanname
405672502CV3297390single nucleotide variantNM_018641.5(CHST12):c.589C>T (p.Arg197Cys)not specified [RCV004441571]uncertain significance724332282433228Humanname
405672509CV3297392single nucleotide variantNM_018641.5(CHST12):c.973G>A (p.Val325Met)not specified [RCV004441573]uncertain significance724336122433612Humanname
407455953CV3422902single nucleotide variantNM_018641.5(CHST12):c.334C>T (p.Arg112Trp)not specified [RCV004610531]uncertain significance724329732432973Humanname
407455958CV3422904single nucleotide variantNM_018641.5(CHST12):c.777C>G (p.Phe259Leu)not specified [RCV004610533]uncertain significance724334162433416Humanname
598215579CV3951807single nucleotide variantNM_018641.5(CHST12):c.388G>T (p.Gly130Cys)not specified [RCV005316784]uncertain significance724330272433027Humanname
598215584CV3951808single nucleotide variantNM_018641.5(CHST12):c.682C>G (p.Arg228Gly)not specified [RCV005316785]uncertain significance724333212433321Humanname
598215597CV3951810single nucleotide variantNM_018641.5(CHST12):c.977A>G (p.Tyr326Cys)not specified [RCV005316787]uncertain significance724336162433616Humanname
15133883CV710939single nucleotide variantNM_018641.5(CHST12):c.629C>G (p.Ala210Gly)not provided [RCV000965029]benign724332682433268Humanname
156090292CV2256497single nucleotide variantNM_018641.5(CHST12):c.1105C>T (p.Arg369Trp)not specified [RCV004118701]uncertain significance724337442433744Humanname
329355443CV2445435single nucleotide variantNM_018641.5(CHST12):c.1097C>G (p.Pro366Arg)not specified [RCV004257497]uncertain significance724337362433736Humanname
329402365CV2454184single nucleotide variantNM_018641.5(CHST12):c.1078C>T (p.Arg360Trp)not specified [RCV004265672]uncertain significance724337172433717Humanname
401742788CV2677680single nucleotide variantNM_018641.5(CHST12):c.1038C>G (p.Asp346Glu)not specified [RCV004291766]uncertain significance724336772433677Humanname
401893768CV2760207single nucleotide variantNM_018641.5(CHST12):c.1238G>A (p.Arg413Gln)not specified [RCV004347384]uncertain significance724338772433877Humanname
401880401CV2783197single nucleotide variantNM_018641.5(CHST12):c.1228A>G (p.Asn410Asp)not specified [RCV004363537]uncertain significance724338672433867Humanname
405672483CV3297385single nucleotide variantNM_018641.5(CHST12):c.1051C>G (p.Gln351Glu)not specified [RCV004441566]uncertain significance724336902433690Humanname
405672487CV3297386single nucleotide variantNM_018641.5(CHST12):c.1062G>C (p.Gln354His)not specified [RCV004441567]uncertain significance724337012433701Humanname
597770809CV3653442single nucleotide variantNM_018641.5(CHST12):c.1205T>C (p.Leu402Pro)not specified [RCV004896996]uncertain significance724338442433844Humanname
597770813CV3653443single nucleotide variantNM_018641.5(CHST12):c.1009G>C (p.Asp337His)not specified [RCV004896997]uncertain significance724336482433648Humanname