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60 records found for search term Hs3st6
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401930216CV2810831single nucleotide variantNM_001009606.4(HS3ST6):c.768G>A (p.Pro256=)not provided [RCV003390616]likely benign1619118511911851Humanname
401904757CV2810832single nucleotide variantNM_001009606.4(HS3ST6):c.516G>A (p.Pro172=)not provided [RCV003395215]likely benign1619121031912103Humanname
156329857CV2213917single nucleotide variantNM_001009606.4(HS3ST6):c.263G>A (p.Arg88Gln)not specified [RCV004083646]uncertain significance1619180611918061Humanname
156144522CV2292264single nucleotide variantNM_001009606.4(HS3ST6):c.181G>A (p.Ala61Thr)not specified [RCV004148300]uncertain significance1619181431918143Humanname
329385802CV2462332single nucleotide variantNM_001009606.4(HS3ST6):c.209C>G (p.Ser70Cys)not specified [RCV004266319]uncertain significance1619181151918115Humanname
401738942CV2708233single nucleotide variantNM_001009606.4(HS3ST6):c.115C>T (p.Leu39Phe)not specified [RCV004311583]uncertain significance1619182091918209Humanname
401864530CV2777873single nucleotide variantNM_001009606.4(HS3ST6):c.254C>A (p.Pro85His)not specified [RCV004347844]uncertain significance1619180701918070Humanname
405799003CV3274070single nucleotide variantNM_001009606.4(HS3ST6):c.230C>G (p.Pro77Arg)not specified [RCV004402395]uncertain significance1619180941918094Humanname
407458120CV3433969single nucleotide variantNM_001009606.4(HS3ST6):c.194C>G (p.Ser65Cys)not specified [RCV004633149]uncertain significance1619181301918130Humanname
597773598CV3689585single nucleotide variantNM_001009606.4(HS3ST6):c.143C>T (p.Pro48Leu)not specified [RCV004928934]uncertain significance1619181811918181Humanname
597773621CV3689590single nucleotide variantNM_001009606.4(HS3ST6):c.296A>G (p.Lys99Arg)not specified [RCV004928939]uncertain significance1619180281918028Humanname
597773634CV3689593single nucleotide variantNM_001009606.4(HS3ST6):c.286G>T (p.Val96Phe)not specified [RCV004928942]uncertain significance1619180381918038Humanname
597773654CV3689598single nucleotide variantNM_001009606.4(HS3ST6):c.239C>A (p.Pro80His)not specified [RCV004928946]uncertain significance1619180851918085Humanname
597773658CV3689599single nucleotide variantNM_001009606.4(HS3ST6):c.148C>A (p.Arg50Ser)not specified [RCV004928947]uncertain significance1619181761918176Humanname
127286740CV1151313single nucleotide variantNM_001009606.4(HS3ST6):c.430A>T (p.Thr144Ser)Angioedema, hereditary, 8 [RCV001507298]pathogenic1619121891912189Human1name
156381962CV2212508single nucleotide variantNM_001009606.4(HS3ST6):c.616G>A (p.Ala206Thr)not specified [RCV004091392]uncertain significance1619120031912003Humanname
156384250CV2231030single nucleotide variantNM_001009606.4(HS3ST6):c.932G>A (p.Arg311His)not specified [RCV004094265]uncertain significance1619116871911687Humanname
155971960CV2238703single nucleotide variantNM_001009606.4(HS3ST6):c.568G>A (p.Asp190Asn)not specified [RCV004107595]uncertain significance1619120511912051Humanname
156264402CV2282656single nucleotide variantNM_001009606.4(HS3ST6):c.869A>G (p.Lys290Arg)not specified [RCV004135209]uncertain significance1619117501911750Humanname
155997950CV2288683single nucleotide variantNM_001009606.4(HS3ST6):c.486G>T (p.Glu162Asp)not specified [RCV004153976]uncertain significance1619121331912133Humanname
155946068CV2301467single nucleotide variantNM_001009606.4(HS3ST6):c.617C>A (p.Ala206Asp)not specified [RCV004162395]uncertain significance1619120021912002Humanname
156175182CV2331076single nucleotide variantNM_001009606.4(HS3ST6):c.616G>T (p.Ala206Ser)not specified [RCV004181690]uncertain significance1619120031912003Humanname
155903053CV2353507single nucleotide variantNM_001009606.4(HS3ST6):c.752G>A (p.Arg251His)not specified [RCV004199492]uncertain significance1619118671911867Humanname
156070461CV2354181single nucleotide variantNM_001009606.4(HS3ST6):c.667G>A (p.Val223Ile)not specified [RCV004206613]uncertain significance1619119521911952Humanname
156208698CV2382538single nucleotide variantNM_001009606.4(HS3ST6):c.613C>T (p.Arg205Cys)not specified [RCV004232870]uncertain significance1619120061912006Humanname
156200630CV2392417single nucleotide variantNM_001009606.4(HS3ST6):c.698A>C (p.Asp233Ala)not specified [RCV004243998]uncertain significance1619119211911921Humanname
156220203CV2393694single nucleotide variantNM_001009606.4(HS3ST6):c.407G>T (p.Trp136Leu)not specified [RCV004231498]uncertain significance1619179171917917Humanname
156144516CV2393695single nucleotide variantNM_001009606.4(HS3ST6):c.410A>T (p.Tyr137Phe)not specified [RCV004231499]uncertain significance1619179141917914Humanname
329387851CV2440166single nucleotide variantNM_001009606.4(HS3ST6):c.757G>A (p.Val253Ile)not specified [RCV004260619]uncertain significance1619118621911862Humanname
329369508CV2461138single nucleotide variantNM_001009606.4(HS3ST6):c.896G>A (p.Arg299His)not specified [RCV004265556]uncertain significance1619117231911723Humanname
401743145CV2694065single nucleotide variantNM_001009606.4(HS3ST6):c.497G>A (p.Arg166His)not specified [RCV004302500]uncertain significance1619121221912122Humanname
401725446CV2697415single nucleotide variantNM_001009606.4(HS3ST6):c.509T>C (p.Met170Thr)not specified [RCV004304164]uncertain significance1619121101912110Humanname
401758291CV2704271single nucleotide variantNM_001009606.4(HS3ST6):c.496C>T (p.Arg166Cys)not specified [RCV004311264]uncertain significance1619121231912123Humanname
401865855CV2755663single nucleotide variantNM_001009606.4(HS3ST6):c.844G>A (p.Ala282Thr)not specified [RCV004342048]uncertain significance1619117751911775Humanname
401873341CV2761431single nucleotide variantNM_001009606.4(HS3ST6):c.494G>A (p.Arg165His)not specified [RCV004334610]uncertain significance1619121251912125Humanname
401878577CV2770681single nucleotide variantNM_001009606.4(HS3ST6):c.751C>T (p.Arg251Cys)not specified [RCV004349729]uncertain significance1619118681911868Humanname
401905557CV2831521single nucleotide variantNM_001009606.4(HS3ST6):c.946C>G (p.Leu316Val)Angioedema, hereditary, 8 [RCV003444514]uncertain significance1619116731911673Human2name
401905557CV2831521single nucleotide variantNM_001009606.4(HS3ST6):c.946C>G (p.Leu316Val)Angioedema, hereditary, 8 [RCV003444514]uncertain significance1619116731911674Human2name
405799011CV3274072single nucleotide variantNM_001009606.4(HS3ST6):c.584T>C (p.Leu195Pro)not specified [RCV004402397]uncertain significance1619120351912035Humanname
405799018CV3274074single nucleotide variantNM_001009606.4(HS3ST6):c.750G>T (p.Glu250Asp)not specified [RCV004402399]uncertain significance1619118691911869Humanname
405799021CV3274075single nucleotide variantNM_001009606.4(HS3ST6):c.752G>C (p.Arg251Pro)not specified [RCV004402400]uncertain significance1619118671911867Humanname
405799024CV3274076single nucleotide variantNM_001009606.4(HS3ST6):c.862T>C (p.Cys288Arg)not specified [RCV004402401]uncertain significance1619117571911757Humanname
405799027CV3274077single nucleotide variantNM_001009606.4(HS3ST6):c.943G>T (p.Ala315Ser)not specified [RCV004402402]uncertain significance1619116761911676Humanname
407458118CV3433968single nucleotide variantNM_001009606.4(HS3ST6):c.541C>T (p.Arg181Trp)not specified [RCV004633148]uncertain significance1619120781912078Humanname
407458123CV3433970single nucleotide variantNM_001009606.4(HS3ST6):c.986G>T (p.Arg329Leu)not specified [RCV004633150]uncertain significance1619116331911633Humanname
407458125CV3433971single nucleotide variantNM_001009606.4(HS3ST6):c.349C>T (p.Arg117Cys)not specified [RCV004633151]uncertain significance1619179751917975Humanname
407458128CV3433972single nucleotide variantNM_001009606.4(HS3ST6):c.908A>G (p.Lys303Arg)not specified [RCV004633152]uncertain significance1619117111911711Humanname
597773593CV3689584single nucleotide variantNM_001009606.4(HS3ST6):c.670C>T (p.Arg224Cys)not specified [RCV004928933]uncertain significance1619119491911949Humanname
597773602CV3689586single nucleotide variantNM_001009606.4(HS3ST6):c.817G>A (p.Val273Ile)not specified [RCV004928935]uncertain significance1619118021911802Humanname
597773608CV3689587single nucleotide variantNM_001009606.4(HS3ST6):c.583C>G (p.Leu195Val)not specified [RCV004928936]uncertain significance1619120361912036Humanname
597773612CV3689588single nucleotide variantNM_001009606.4(HS3ST6):c.763G>A (p.Asp255Asn)not specified [RCV004928937]uncertain significance1619118561911856Humanname
597773617CV3689589single nucleotide variantNM_001009606.4(HS3ST6):c.785G>A (p.Arg262His)not specified [RCV004928938]uncertain significance1619118341911834Humanname
597773625CV3689591single nucleotide variantNM_001009606.4(HS3ST6):c.452T>C (p.Met151Thr)not specified [RCV004928940]uncertain significance1619121671912167Humanname
597773629CV3689592single nucleotide variantNM_001009606.4(HS3ST6):c.685G>T (p.Ala229Ser)not specified [RCV004928941]uncertain significance1619119341911934Humanname
597773638CV3689594single nucleotide variantNM_001009606.4(HS3ST6):c.308C>G (p.Thr103Arg)not specified [RCV004928943]uncertain significance1619180161918016Humanname
597773646CV3689595single nucleotide variantNM_001009606.4(HS3ST6):c.608G>C (p.Ser203Thr)not specified [RCV004928944]uncertain significance1619120111912011Humanname
597773650CV3689597single nucleotide variantNM_001009606.4(HS3ST6):c.575C>T (p.Ala192Val)not specified [RCV004928945]uncertain significance1619120441912044Humanname
598193038CV3972031single nucleotide variantNM_001009606.4(HS3ST6):c.973C>T (p.Arg325Trp)not specified [RCV005354575]uncertain significance1619116461911646Humanname
598255495CV3972032single nucleotide variantNM_001009606.4(HS3ST6):c.931C>T (p.Arg311Cys)not specified [RCV005346569]uncertain significance1619116881911688Humanname
598205484CV3972033single nucleotide variantNM_001009606.4(HS3ST6):c.436G>A (p.Asp146Asn)not specified [RCV005337617]uncertain significance1619121831912183Humanname