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37 records found for search term Cela3b
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
617153007CV4020775single nucleotide variantNM_007352.4(CELA3B):c.129+1G>Anot provided [RCV005428528]likely benign12197845521978455Humanname
405744965CV3303823single nucleotide variantNM_007352.4(CELA3B):c.8T>C (p.Leu3Pro)not specified [RCV004431273]uncertain significance12197704721977047Humanname
156257067CV2204554single nucleotide variantNM_007352.4(CELA3B):c.11G>A (p.Arg4Gln)not specified [RCV004081668]uncertain significance12197705021977050Humanname
401895917CV2779587single nucleotide variantNM_007352.4(CELA3B):c.10C>G (p.Arg4Gly)not specified [RCV004351299]uncertain significance12197704921977049Humanname
15190058CV696472single nucleotide variantNM_007352.4(CELA3B):c.189C>T (p.Ile63=)not provided [RCV000954363]benign12198088321980883Humanname
156098273CV2253254single nucleotide variantNM_007352.4(CELA3B):c.92A>G (p.Asn31Ser)not specified [RCV004122795]uncertain significance12197841721978417Humanname
401935461CV2812452single nucleotide variantNM_007352.4(CELA3B):c.91A>C (p.Asn31His)not provided [RCV003412890]likely benign12197841621978416Humanname
405263694CV3185218single nucleotide variantNM_007352.4(CELA3B):c.411C>T (p.Asp137=)not provided [RCV003885782]benign12198374221983742Humanname
597768151CV3648989single nucleotide variantNM_007352.4(CELA3B):c.46T>G (p.Ser16Ala)not specified [RCV004896493]uncertain significance12197837121978371Humanname
156031317CV2239106single nucleotide variantNM_007352.4(CELA3B):c.239C>T (p.Thr80Ile)not specified [RCV004112105]uncertain significance12198104921981049Humanname
156362053CV2323017single nucleotide variantNM_007352.4(CELA3B):c.214G>A (p.Gly72Ser)not specified [RCV004185445]uncertain significance12198090821980908Humanname
405744938CV3303819single nucleotide variantNM_007352.4(CELA3B):c.239C>A (p.Thr80Asn)not specified [RCV004431269]uncertain significance12198104921981049Humanname
597768141CV3648987single nucleotide variantNM_007352.4(CELA3B):c.170C>T (p.Thr57Ile)not specified [RCV004896491]uncertain significance12198086421980864Humanname
597768145CV3648988single nucleotide variantNM_007352.4(CELA3B):c.284G>A (p.Gly95Asp)not specified [RCV004896492]uncertain significance12198109421981094Humanname
598194663CV3951176single nucleotide variantNM_007352.4(CELA3B):c.100G>A (p.Asp34Asn)not specified [RCV005313204]uncertain significance12197842521978425Humanname
21067309CV792637single nucleotide variantNM_007352.4(CELA3B):c.268C>T (p.Arg90Cys)not provided [RCV000991238]uncertain significance12198107821981078Humanname
156077990CV2198271single nucleotide variantNM_007352.4(CELA3B):c.505G>A (p.Gly169Arg)not specified [RCV004081827]uncertain significance12198419421984194Humanname
156123566CV2234056single nucleotide variantNM_007352.4(CELA3B):c.607G>A (p.Val203Met)not specified [RCV004106165]uncertain significance12198429621984296Humanname
155989104CV2285599single nucleotide variantNM_007352.4(CELA3B):c.622G>T (p.Asp208Tyr)not specified [RCV004141469]uncertain significance12198431121984311Humanname
156088233CV2359217single nucleotide variantNM_007352.4(CELA3B):c.706A>C (p.Thr236Pro)not specified [RCV004212512]uncertain significance12198659421986594Humanname
156090382CV2375227single nucleotide variantNM_007352.4(CELA3B):c.347C>T (p.Ser116Leu)not specified [RCV004230260]likely benign12198115721981157Humanname
329386803CV2439406single nucleotide variantNM_007352.4(CELA3B):c.790G>C (p.Glu264Gln)not specified [RCV004249698]uncertain significance12198667821986678Humanname
401747386CV2696683single nucleotide variantNM_007352.4(CELA3B):c.577T>C (p.Trp193Arg)not specified [RCV004290663]uncertain significance12198426621984266Humanname
401752877CV2703369single nucleotide variantNM_007352.4(CELA3B):c.299T>C (p.Ile100Thr)not specified [RCV004315716]uncertain significance12198110921981109Humanname
401860416CV2768583single nucleotide variantNM_007352.4(CELA3B):c.781G>A (p.Asp261Asn)not specified [RCV004344445]uncertain significance12198666921986669Humanname
405744943CV3303820single nucleotide variantNM_007352.4(CELA3B):c.314G>A (p.Gly105Glu)not specified [RCV004431270]likely benign12198112421981124Humanname
405744949CV3303821single nucleotide variantNM_007352.4(CELA3B):c.731G>A (p.Cys244Tyr)not specified [RCV004431271]uncertain significance12198661921986619Humanname
405744956CV3303822single nucleotide variantNM_007352.4(CELA3B):c.802G>A (p.Ala268Thr)not specified [RCV004431272]uncertain significance12198926821989268Humanname
407460990CV3418796single nucleotide variantNM_007352.4(CELA3B):c.302C>G (p.Pro101Arg)not specified [RCV004612497]uncertain significance12198111221981112Humanname
407460994CV3418797single nucleotide variantNM_007352.4(CELA3B):c.359G>C (p.Cys120Ser)not specified [RCV004612498]uncertain significance12198116921981169Humanname
407460999CV3418798single nucleotide variantNM_007352.4(CELA3B):c.779T>C (p.Ile260Thr)not specified [RCV004612499]uncertain significance12198666721986667Humanname
407461003CV3418799single nucleotide variantNM_007352.4(CELA3B):c.313G>T (p.Gly105Trp)not specified [RCV004612500]uncertain significance12198112321981123Humanname
597768155CV3648990single nucleotide variantNM_007352.4(CELA3B):c.316G>T (p.Asp106Tyr)not specified [RCV004896494]uncertain significance12198112621981126Humanname
597768161CV3648991single nucleotide variantNM_007352.4(CELA3B):c.807C>A (p.Ser269Arg)not specified [RCV004896495]uncertain significance12198927321989273Humanname
598194656CV3951175single nucleotide variantNM_007352.4(CELA3B):c.544G>A (p.Val182Met)not specified [RCV005313203]uncertain significance12198423321984233Humanname
617152346CV4020715single nucleotide variantNM_007352.4(CELA3B):c.415G>A (p.Val139Ile)not provided [RCV005427972]likely benign12198374621983746Humanname
15100629CV718664single nucleotide variantNM_007352.4(CELA3B):c.391C>T (p.Arg131Cys)not provided [RCV000892141]benign12198372221983722Humanname