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22 records found for search term Ceacam19
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597767631CV3648854single nucleotide variantNM_001127893.3(CEACAM19):c.85G>A (p.Gly29Ser)not specified [RCV004896394]uncertain significance194467262544672625Humanname
156294657CV2302975single nucleotide variantNM_001127893.3(CEACAM19):c.138C>G (p.Asn46Lys)not specified [RCV004156775]uncertain significance194467267844672678Humanname
156263997CV2384533single nucleotide variantNM_001127893.3(CEACAM19):c.176C>T (p.Thr59Ile)not specified [RCV004232331]uncertain significance194467271644672716Humanname
329369443CV2424822single nucleotide variantNM_001127893.3(CEACAM19):c.217G>A (p.Gly73Arg)not specified [RCV004248710]uncertain significance194467275744672757Humanname
401719386CV2706281single nucleotide variantNM_001127893.3(CEACAM19):c.126G>T (p.Gln42His)not specified [RCV004314942]uncertain significance194467266644672666Humanname
405743775CV3303684single nucleotide variantNM_001127893.3(CEACAM19):c.205G>A (p.Glu69Lys)not specified [RCV004431134]uncertain significance194467274544672745Humanname
405743779CV3303685single nucleotide variantNM_001127893.3(CEACAM19):c.212C>T (p.Thr71Met)not specified [RCV004431135]likely benign194467275244672752Humanname
597767621CV3648852single nucleotide variantNM_001127893.3(CEACAM19):c.123G>C (p.Glu41Asp)not specified [RCV004896392]uncertain significance194467266344672663Humanname
156288879CV2229822single nucleotide variantNM_001127893.3(CEACAM19):c.334G>A (p.Ala112Thr)not specified [RCV004105393]uncertain significance194467287444672874Humanname
156045376CV2234426single nucleotide variantNM_001127893.3(CEACAM19):c.703G>T (p.Ala235Ser)not specified [RCV004100639]uncertain significance194468033144680331Humanname
155975440CV2342665single nucleotide variantNM_001127893.3(CEACAM19):c.329G>A (p.Arg110His)not specified [RCV004196747]uncertain significance194467286944672869Humanname
156108248CV2390217single nucleotide variantNM_001127893.3(CEACAM19):c.805C>G (p.Pro269Ala)not specified [RCV004240598]uncertain significance194468257944682579Humanname
401876760CV2754473single nucleotide variantNM_001127893.3(CEACAM19):c.662T>G (p.Met221Arg)not specified [RCV004336683]uncertain significance194468029044680290Humanname
401855237CV2757198single nucleotide variantNM_001127893.3(CEACAM19):c.527G>A (p.Cys176Tyr)not specified [RCV004338802]uncertain significance194467637344676373Humanname
405743786CV3303686single nucleotide variantNM_001127893.3(CEACAM19):c.448A>T (p.Thr150Ser)not specified [RCV004431136]uncertain significance194467629444676294Humanname
405743790CV3303687single nucleotide variantNM_001127893.3(CEACAM19):c.710A>T (p.Asp237Val)not specified [RCV004431137]uncertain significance194468123044681230Humanname
407460837CV3418733single nucleotide variantNM_001127893.3(CEACAM19):c.734C>G (p.Pro245Arg)not specified [RCV004612434]uncertain significance194468125444681254Humanname
407460841CV3418734single nucleotide variantNM_001127893.3(CEACAM19):c.571C>T (p.His191Tyr)not specified [RCV004612435]uncertain significance194467641744676417Humanname
597767611CV3648850single nucleotide variantNM_001127893.3(CEACAM19):c.490A>T (p.Ile164Phe)not specified [RCV004896390]uncertain significance194467633644676336Humanname
597767616CV3648851single nucleotide variantNM_001127893.3(CEACAM19):c.395T>C (p.Met132Thr)not specified [RCV004896391]uncertain significance194467293544672935Humanname
597767626CV3648853single nucleotide variantNM_001127893.3(CEACAM19):c.452A>C (p.His151Pro)not specified [RCV004896393]uncertain significance194467629844676298Humanname
598193870CV3940482single nucleotide variantNM_001127893.3(CEACAM19):c.854T>C (p.Leu285Pro)not specified [RCV005313066]uncertain significance194468344444683444Humanname