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Variants search result for Homo sapiens
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36 records found for search term Ptcd2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156090445CV2299963single nucleotide variantNM_024754.5(PTCD2):c.65A>C (p.Gln22Pro)not specified [RCV004151181]uncertain significance57232044772320447Humanname
156081141CV2368770single nucleotide variantNM_024754.5(PTCD2):c.35C>G (p.Pro12Arg)not specified [RCV004214648]uncertain significance57232041772320417Humanname
405672558CV3377609single nucleotide variantNM_024754.5(PTCD2):c.32G>T (p.Arg11Leu)not specified [RCV004515469]uncertain significance57232041472320414Humanname
156291073CV2324969single nucleotide variantNM_024754.5(PTCD2):c.137A>T (p.Tyr46Phe)not specified [RCV004175222]uncertain significance57232218172322181Humanname
156190267CV2384963single nucleotide variantNM_024754.5(PTCD2):c.101C>T (p.Ser34Phe)not specified [RCV004226191]uncertain significance57232048372320483Humanname
329398274CV2464379single nucleotide variantNM_024754.5(PTCD2):c.276G>C (p.Lys92Asn)not specified [RCV004276321]uncertain significance57232666772326667Humanname
405672549CV3377607single nucleotide variantNM_024754.5(PTCD2):c.244A>G (p.Lys82Glu)not specified [RCV004515467]likely benign57232663572326635Humanname
598171327CV3908287single nucleotide variantNM_024754.5(PTCD2):c.256C>A (p.Gln86Lys)not specified [RCV005263324]uncertain significance57232664772326647Humanname
598171333CV3908288single nucleotide variantNM_024754.5(PTCD2):c.290C>T (p.Thr97Ile)not specified [RCV005263325]uncertain significance57232668172326681Humanname
156370012CV2204089single nucleotide variantNM_024754.5(PTCD2):c.401C>T (p.Pro134Leu)not specified [RCV004076904]uncertain significance57233130872331308Humanname
156273416CV2247647single nucleotide variantNM_024754.5(PTCD2):c.433C>G (p.Leu145Val)not specified [RCV004110979]uncertain significance57233134072331340Humanname
155927360CV2285119single nucleotide variantNM_024754.5(PTCD2):c.922C>T (p.His308Tyr)not specified [RCV004145343]uncertain significance57235273472352734Humanname
156290330CV2342578single nucleotide variantNM_024754.5(PTCD2):c.716G>C (p.Arg239Thr)not specified [RCV004196672]uncertain significance57233869872338698Humanname
155902327CV2356436single nucleotide variantNM_024754.5(PTCD2):c.974T>C (p.Val325Ala)not specified [RCV004206235]uncertain significance57235823472358234Humanname
156304497CV2369110single nucleotide variantNM_024754.5(PTCD2):c.854T>A (p.Met285Lys)not specified [RCV004214949]uncertain significance57235266672352666Humanname
329399346CV2470053single nucleotide variantNM_024754.5(PTCD2):c.715A>G (p.Arg239Gly)not specified [RCV004287322]uncertain significance57233869772338697Humanname
401765845CV2683443single nucleotide variantNM_024754.5(PTCD2):c.814T>G (p.Cys272Gly)not specified [RCV004288205]uncertain significance57234302272343022Humanname
401892266CV2776036single nucleotide variantNM_024754.5(PTCD2):c.631T>C (p.Tyr211His)not specified [RCV004353145]uncertain significance57233587772335877Humanname
405672553CV3377608single nucleotide variantNM_024754.5(PTCD2):c.313C>T (p.Arg105Trp)not specified [RCV004515468]uncertain significance57232670472326704Humanname
405672562CV3377610single nucleotide variantNM_024754.5(PTCD2):c.573G>T (p.Met191Ile)not specified [RCV004515470]uncertain significance57233581972335819Humanname
405672565CV3377611single nucleotide variantNM_024754.5(PTCD2):c.772G>A (p.Val258Met)not specified [RCV004515471]likely benign57234298072342980Humanname
407531860CV3472005single nucleotide variantNM_024754.5(PTCD2):c.387G>C (p.Glu129Asp)not specified [RCV004657821]uncertain significance57233129472331294Humanname
407531862CV3472006single nucleotide variantNM_024754.5(PTCD2):c.500C>T (p.Ser167Leu)not specified [RCV004657822]uncertain significance57233504972335049Humanname
597750843CV3592244single nucleotide variantNM_024754.5(PTCD2):c.508A>G (p.Ile170Val)not specified [RCV004846525]uncertain significance57233505772335057Humanname
597750848CV3592245single nucleotide variantNM_024754.5(PTCD2):c.608A>G (p.Tyr203Cys)not specified [RCV004846526]uncertain significance57233585472335854Humanname
597750851CV3592246single nucleotide variantNM_024754.5(PTCD2):c.325G>A (p.Glu109Lys)not specified [RCV004846527]uncertain significance57232671672326716Humanname
597750861CV3592248single nucleotide variantNM_024754.5(PTCD2):c.668C>G (p.Thr223Ser)not specified [RCV004846529]uncertain significance57233865072338650Humanname
597750871CV3592250single nucleotide variantNM_024754.5(PTCD2):c.677G>A (p.Arg226Lys)not specified [RCV004846531]uncertain significance57233865972338659Humanname
597750876CV3592251single nucleotide variantNM_024754.5(PTCD2):c.970G>C (p.Asp324His)not specified [RCV004846532]uncertain significance57235823072358230Humanname
401742431CV2677586single nucleotide variantNM_024754.5(PTCD2):c.1100T>C (p.Leu367Pro)not specified [RCV004291685]uncertain significance57235836072358360Humanname
401896190CV2773777single nucleotide variantNM_024754.5(PTCD2):c.1057G>C (p.Val353Leu)not specified [RCV004356443]likely benign57235831772358317Humanname
405672544CV3377606single nucleotide variantNM_024754.5(PTCD2):c.1013C>T (p.Thr338Ile)not specified [RCV004515466]uncertain significance57235827372358273Humanname
597750866CV3592249single nucleotide variantNM_024754.5(PTCD2):c.1123C>T (p.Arg375Cys)not specified [RCV004846530]uncertain significance57235838372358383Humanname
597750881CV3592252single nucleotide variantNM_024754.5(PTCD2):c.1087T>A (p.Ser363Thr)not specified [RCV004846533]uncertain significance57235834772358347Humanname
598171343CV3908290single nucleotide variantNM_024754.5(PTCD2):c.1126C>A (p.Arg376Ser)not specified [RCV005263327]uncertain significance57235838672358386Humanname
8631688CV86892single nucleotide variantNM_024754.4(PTCD2):c.1072C>T (p.Pro358Ser)Malignant melanoma [RCV000066983]not provided57235833272358332Humanname