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32 records found for search term Pcsk1n
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156336603CV2360774single nucleotide variantNM_013271.5(PCSK1N):c.121C>T (p.Arg41Cys)not specified [RCV004213551]uncertain significanceX4883233548832335Humanname
329356090CV2445621single nucleotide variantNM_013271.5(PCSK1N):c.167C>T (p.Pro56Leu)not specified [RCV004259705]uncertain significanceX4883228948832289Humanname
329402880CV2451494single nucleotide variantNM_013271.5(PCSK1N):c.287A>C (p.Gln96Pro)not specified [RCV004272156]uncertain significanceX4883216948832169Humanname
401759046CV2694403single nucleotide variantNM_013271.5(PCSK1N):c.220G>A (p.Glu74Lys)not specified [RCV004304585]uncertain significanceX4883223648832236Humanname
405762358CV3364839single nucleotide variantNM_013271.5(PCSK1N):c.155A>G (p.Glu52Gly)not specified [RCV004500854]uncertain significanceX4883230148832301Humanname
156147732CV2196982single nucleotide variantNM_013271.5(PCSK1N):c.379G>T (p.Asp127Tyr)not specified [RCV004071437]uncertain significanceX4883207748832077Humanname
156301074CV2248925single nucleotide variantNM_013271.5(PCSK1N):c.454G>A (p.Ala152Thr)not specified [RCV004115929]uncertain significanceX4883200248832002Humanname
156236503CV2268774single nucleotide variantNM_013271.5(PCSK1N):c.452C>A (p.Ala151Glu)not specified [RCV004124161]uncertain significanceX4883200448832004Humanname
155929030CV2281354single nucleotide variantNM_013271.5(PCSK1N):c.631G>T (p.Gly211Trp)not specified [RCV004141157]uncertain significanceX4883141248831412Humanname
156182940CV2294769single nucleotide variantNM_013271.5(PCSK1N):c.602G>T (p.Arg201Leu)not specified [RCV004162291]uncertain significanceX4883144148831441Humanname
155906902CV2302112single nucleotide variantNM_013271.5(PCSK1N):c.313G>C (p.Val105Leu)not specified [RCV004159133]uncertain significanceX4883214348832143Humanname
155963450CV2308276single nucleotide variantNM_013271.5(PCSK1N):c.314T>C (p.Val105Ala)not specified [RCV004164769]uncertain significanceX4883214248832142Humanname
156169410CV2317077single nucleotide variantNM_013271.5(PCSK1N):c.652C>T (p.Leu218Phe)not specified [RCV004174563]uncertain significanceX4883139148831391Humanname
155967017CV2329866single nucleotide variantNM_013271.5(PCSK1N):c.736G>C (p.Glu246Gln)not specified [RCV004183324]uncertain significanceX4883130748831307Humanname
156290997CV2342793single nucleotide variantNM_013271.5(PCSK1N):c.388G>C (p.Asp130His)not specified [RCV004189834]uncertain significanceX4883206848832068Humanname
156236292CV2346430single nucleotide variantNM_013271.5(PCSK1N):c.565G>T (p.Asp189Tyr)not specified [RCV004203908]uncertain significanceX4883189148831891Humanname
156068721CV2356916single nucleotide variantNM_013271.5(PCSK1N):c.624C>G (p.Asp208Glu)not specified [RCV004204290]uncertain significanceX4883141948831419Humanname
401769141CV2693317single nucleotide variantNM_013271.5(PCSK1N):c.746C>T (p.Ala249Val)not specified [RCV004295280]uncertain significanceX4883129748831297Humanname
405762364CV3364840single nucleotide variantNM_013271.5(PCSK1N):c.350G>T (p.Arg117Leu)not specified [RCV004500855]uncertain significanceX4883210648832106Humanname
405762370CV3364841single nucleotide variantNM_013271.5(PCSK1N):c.376G>C (p.Asp126His)not specified [RCV004500856]uncertain significanceX4883208048832080Humanname
405762378CV3364842single nucleotide variantNM_013271.5(PCSK1N):c.442G>A (p.Ala148Thr)not specified [RCV004500857]uncertain significanceX4883201448832014Humanname
405762384CV3364843single nucleotide variantNM_013271.5(PCSK1N):c.466C>G (p.Pro156Ala)not specified [RCV004500858]uncertain significanceX4883199048831990Humanname
405762397CV3364845single nucleotide variantNM_013271.5(PCSK1N):c.577G>A (p.Glu193Lys)not specified [RCV004500860]uncertain significanceX4883187948831879Humanname
405762404CV3364846single nucleotide variantNM_013271.5(PCSK1N):c.776C>T (p.Pro259Leu)not specified [RCV004500861]uncertain significanceX4883126748831267Humanname
407523765CV3460034single nucleotide variantNM_013271.5(PCSK1N):c.472C>T (p.Pro158Ser)not specified [RCV004653416]uncertain significanceX4883198448831984Humanname
407523768CV3460035single nucleotide variantNM_013271.5(PCSK1N):c.403C>A (p.Gln135Lys)not specified [RCV004653417]uncertain significanceX4883205348832053Humanname
407463128CV3460036single nucleotide variantNM_013271.5(PCSK1N):c.743C>T (p.Pro248Leu)not specified [RCV004659601]uncertain significanceX4883130048831300Humanname
597697531CV3571950single nucleotide variantNM_013271.5(PCSK1N):c.497C>A (p.Pro166His)not specified [RCV004839338]uncertain significanceX4883195948831959Humanname
597697542CV3571952single nucleotide variantNM_013271.5(PCSK1N):c.329T>A (p.Leu110Gln)not specified [RCV004839339]uncertain significanceX4883212748832127Humanname
597697548CV3571953single nucleotide variantNM_013271.5(PCSK1N):c.703G>C (p.Val235Leu)not specified [RCV004839340]uncertain significanceX4883134048831340Humanname
598165125CV4006032single nucleotide variantNM_013271.5(PCSK1N):c.430C>T (p.Arg144Cys)not specified [RCV005391279]uncertain significanceX4883202648832026Humanname
598165133CV4006033single nucleotide variantNM_013271.5(PCSK1N):c.469G>A (p.Ala157Thr)not specified [RCV005391280]uncertain significanceX4883198748831987Humanname