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Variants search result for Homo sapiens
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56 records found for search term Pcdhb9
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156052151CV2336715single nucleotide variantNM_019119.5(PCDHB9):c.10A>G (p.Arg4Gly)not specified [RCV004196955]likely benign5141187328141187328Humanname
156159606CV2322753single nucleotide variantNM_019119.5(PCDHB9):c.77C>T (p.Ala26Val)not specified [RCV004182863]uncertain significance5141187395141187395Humanname
401915142CV2825317single nucleotide variantNM_019119.5(PCDHB9):c.585G>T (p.Val195=)not provided [RCV003428637]likely benign5141187903141187903Humanname
401915144CV2825318single nucleotide variantNM_019119.5(PCDHB9):c.690T>C (p.Ile230=)not provided [RCV003428638]likely benign5141188008141188008Humanname
401917927CV2825319single nucleotide variantNM_019119.5(PCDHB9):c.858A>G (p.Glu286=)not provided [RCV003429834]likely benign5141188176141188176Humanname
597737952CV3575231single nucleotide variantNM_019119.5(PCDHB9):c.71C>T (p.Ser24Phe)not specified [RCV004843973]uncertain significance5141187389141187389Humanname
597737935CV3575234single nucleotide variantNM_019119.5(PCDHB9):c.80G>A (p.Gly27Asp)not specified [RCV004843976]uncertain significance5141187398141187398Humanname
598270770CV3996226single nucleotide variantNM_019119.5(PCDHB9):c.86G>T (p.Gly29Val)not specified [RCV005388950]uncertain significance5141187404141187404Humanname
598195610CV3996232single nucleotide variantNM_019119.5(PCDHB9):c.61T>G (p.Trp21Gly)not specified [RCV005397561]uncertain significance5141187379141187379Humanname
156296428CV2310413single nucleotide variantNM_019119.5(PCDHB9):c.253C>T (p.Leu85Phe)not specified [RCV004163454]uncertain significance5141187571141187571Humanname
329399418CV2446995single nucleotide variantNM_019119.5(PCDHB9):c.181G>A (p.Ala61Thr)not specified [RCV004257832]uncertain significance5141187499141187499Humanname
401732633CV2708914single nucleotide variantNM_019119.5(PCDHB9):c.168G>T (p.Glu56Asp)not specified [RCV004309883]uncertain significance5141187486141187486Humanname
401917929CV2825320single nucleotide variantNM_019119.5(PCDHB9):c.1200T>C (p.Phe400=)not provided [RCV003429835]likely benign5141188518141188518Humanname
401917930CV2825321single nucleotide variantNM_019119.5(PCDHB9):c.1647A>G (p.Val549=)not provided [RCV003429836]likely benign5141188965141188965Humanname
597737908CV3575240single nucleotide variantNM_019119.5(PCDHB9):c.289G>T (p.Gly97Cys)not specified [RCV004843981]uncertain significance5141187607141187607Humanname
598270751CV3996229single nucleotide variantNM_019119.5(PCDHB9):c.220T>C (p.Tyr74His)not specified [RCV005388953]likely benign5141187538141187538Humanname
598270737CV3996231single nucleotide variantNM_019119.5(PCDHB9):c.136G>C (p.Val46Leu)not specified [RCV005388955]uncertain significance5141187454141187454Humanname
8631442CV86629single nucleotide variantNM_019119.4(PCDHB9):c.1845C>T (p.Phe615=)Malignant melanoma [RCV000066720]not provided5141189163141189163Humanname
155931000CV2220954single nucleotide variantNM_019119.5(PCDHB9):c.371G>A (p.Arg124Lys)not specified [RCV004092643]uncertain significance5141187689141187689Humanname
155933632CV2228957single nucleotide variantNM_019119.5(PCDHB9):c.887C>T (p.Pro296Leu)not specified [RCV004098750]uncertain significance5141188205141188205Humanname
156026037CV2242310single nucleotide variantNM_019119.5(PCDHB9):c.604C>G (p.Arg202Gly)not specified [RCV004111325]uncertain significance5141187922141187922Humanname
156218456CV2253952single nucleotide variantNM_019119.5(PCDHB9):c.746C>A (p.Thr249Asn)not specified [RCV004127626]uncertain significance5141188064141188064Humanname
156141765CV2288582single nucleotide variantNM_019119.5(PCDHB9):c.421A>G (p.Lys141Glu)not specified [RCV004152102]uncertain significance5141187739141187739Humanname
156086501CV2289963single nucleotide variantNM_019119.5(PCDHB9):c.456T>G (p.Phe152Leu)not specified [RCV004150612]uncertain significance5141187774141187774Humanname
156200037CV2293867single nucleotide variantNM_019119.5(PCDHB9):c.830T>C (p.Val277Ala)not specified [RCV004155127]uncertain significance5141188148141188148Humanname
156201912CV2313181single nucleotide variantNM_019119.5(PCDHB9):c.685C>G (p.Arg229Gly)not specified [RCV004161440]uncertain significance5141188003141188003Humanname
156357345CV2318276single nucleotide variantNM_019119.5(PCDHB9):c.686G>A (p.Arg229His)not specified [RCV004179450]uncertain significance5141188004141188004Humanname
155926794CV2365815single nucleotide variantNM_019119.5(PCDHB9):c.886C>T (p.Pro296Ser)not specified [RCV004214350]uncertain significance5141188204141188204Humanname
155959906CV2390608single nucleotide variantNM_019119.5(PCDHB9):c.543A>C (p.Lys181Asn)not specified [RCV004239133]uncertain significance5141187861141187861Humanname
329395388CV2458318single nucleotide variantNM_019119.5(PCDHB9):c.496A>G (p.Ser166Gly)not specified [RCV004265961]likely benign5141187814141187814Humanname
401767039CV2680226single nucleotide variantNM_019119.5(PCDHB9):c.617A>G (p.Glu206Gly)not specified [RCV004286700]likely benign5141187935141187935Humanname
401733993CV2697924single nucleotide variantNM_019119.5(PCDHB9):c.904T>A (p.Phe302Ile)not specified [RCV004300629]uncertain significance5141188222141188222Humanname
401888997CV2761638single nucleotide variantNM_019119.5(PCDHB9):c.325T>A (p.Leu109Ile)not specified [RCV004337258]uncertain significance5141187643141187643Humanname
401891464CV2779140single nucleotide variantNM_019119.5(PCDHB9):c.641C>T (p.Ala214Val)not specified [RCV004349057]uncertain significance5141187959141187959Humanname
405743872CV3368110single nucleotide variantNM_019119.5(PCDHB9):c.451G>C (p.Ala151Pro)not specified [RCV004498177]uncertain significance5141187769141187769Humanname
405743882CV3368111single nucleotide variantNM_019119.5(PCDHB9):c.543A>T (p.Lys181Asn)not specified [RCV004498178]uncertain significance5141187861141187861Humanname
405743890CV3368112single nucleotide variantNM_019119.5(PCDHB9):c.686G>T (p.Arg229Leu)not specified [RCV004498179]uncertain significance5141188004141188004Humanname
405743902CV3368114single nucleotide variantNM_019119.5(PCDHB9):c.896G>A (p.Gly299Glu)not specified [RCV004498181]uncertain significance5141188214141188214Humanname
407523494CV3463209single nucleotide variantNM_019119.5(PCDHB9):c.711C>A (p.Asp237Glu)not specified [RCV004653232]uncertain significance5141188029141188029Humanname
407462834CV3463210single nucleotide variantNM_019119.5(PCDHB9):c.824C>A (p.Ala275Glu)not specified [RCV004659464]uncertain significance5141188142141188142Humanname
597737945CV3575232single nucleotide variantNM_019119.5(PCDHB9):c.682A>C (p.Ile228Leu)not specified [RCV004843974]uncertain significance5141188000141188000Humanname
597737940CV3575233single nucleotide variantNM_019119.5(PCDHB9):c.502C>G (p.Gln168Glu)not specified [RCV004843975]uncertain significance5141187820141187820Humanname
597737930CV3575235single nucleotide variantNM_019119.5(PCDHB9):c.769G>A (p.Val257Ile)not specified [RCV004843977]uncertain significance5141188087141188087Humanname
597737925CV3575236single nucleotide variantNM_019119.5(PCDHB9):c.776C>T (p.Ser259Phe)not specified [RCV004843978]uncertain significance5141188094141188094Humanname
597737920CV3575237single nucleotide variantNM_019119.5(PCDHB9):c.859G>A (p.Asp287Asn)not specified [RCV004843979]uncertain significance5141188177141188177Humanname
597756357CV3575238single nucleotide variantNM_019119.5(PCDHB9):c.452C>T (p.Ala151Val)not specified [RCV004848107]uncertain significance5141187770141187770Humanname
597737915CV3575239single nucleotide variantNM_019119.5(PCDHB9):c.923A>G (p.Asp308Gly)not specified [RCV004843980]uncertain significance5141188241141188241Humanname
597737731CV3575241single nucleotide variantNM_019119.5(PCDHB9):c.776C>A (p.Ser259Tyr)not specified [RCV004843982]uncertain significance5141188094141188094Humanname
597737653CV3575242single nucleotide variantNM_019119.5(PCDHB9):c.412A>G (p.Met138Val)not specified [RCV004843983]uncertain significance5141187730141187730Humanname
597737657CV3575243single nucleotide variantNM_019119.5(PCDHB9):c.394G>C (p.Val132Leu)not specified [RCV004843984]uncertain significance5141187712141187712Humanname
598270764CV3996227single nucleotide variantNM_019119.5(PCDHB9):c.641C>A (p.Ala214Glu)not specified [RCV005388951]uncertain significance5141187959141187959Humanname
598270757CV3996228single nucleotide variantNM_019119.5(PCDHB9):c.851C>T (p.Ala284Val)not specified [RCV005388952]uncertain significance5141188169141188169Humanname
598270730CV3996233single nucleotide variantNM_019119.5(PCDHB9):c.605G>A (p.Arg202Gln)not specified [RCV005388956]uncertain significance5141187923141187923Humanname
155966762CV2261083single nucleotide variantNM_019119.5(PCDHB9):c.2195T>A (p.Phe732Tyr)not specified [RCV004127990]uncertain significance5141189513141189513Humanname
156147451CV2377249single nucleotide variantNM_019119.5(PCDHB9):c.2182C>A (p.Pro728Thr)not specified [RCV004232308]uncertain significance5141189500141189500Humanname
8625934CV81073single nucleotide variantNM_019119.4(PCDHB9):c.1219G>A (p.Gly407Ser)Malignant melanoma [RCV000061151]not provided5141188537141188537Humanname