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25 records found for search term Samd10
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401723850CV2737894single nucleotide variantNM_080621.5(SAMD10):c.92-4A>Gnot provided [RCV003315066]likely benign206397741063977410Humanname
156204527CV2331687single nucleotide variantNM_080621.5(SAMD10):c.80G>C (p.Arg27Pro)not specified [RCV004184316]uncertain significance206397938863979388Humanname
156326936CV2332027single nucleotide variantNM_080621.5(SAMD10):c.77G>A (p.Arg26His)not specified [RCV004189081]uncertain significance206397939163979391Humanname
156088374CV2201981single nucleotide variantNM_080621.5(SAMD10):c.195G>C (p.Trp65Cys)not specified [RCV004075907]uncertain significance206397730363977303Humanname
155971158CV2214070single nucleotide variantNM_080621.5(SAMD10):c.206G>A (p.Arg69His)not specified [RCV004084116]uncertain significance206397729263977292Humanname
155931051CV2220965single nucleotide variantNM_080621.5(SAMD10):c.278G>A (p.Arg93Gln)not specified [RCV004092652]uncertain significance206397713863977138Humanname
156181760CV2298557single nucleotide variantNM_080621.5(SAMD10):c.121C>T (p.Leu41Phe)not specified [RCV004162210]uncertain significance206397737763977377Humanname
156187900CV2328477single nucleotide variantNM_080621.5(SAMD10):c.275G>A (p.Gly92Asp)not specified [RCV004175858]uncertain significance206397714163977141Humanname
401766660CV2725661single nucleotide variantNM_080621.5(SAMD10):c.215G>A (p.Arg72Lys)not specified [RCV004322032]uncertain significance206397728363977283Humanname
401865337CV2778700single nucleotide variantNM_080621.5(SAMD10):c.115C>T (p.Arg39Trp)not specified [RCV004346616]uncertain significance206397738363977383Humanname
405721997CV3320384single nucleotide variantNM_080621.5(SAMD10):c.277C>T (p.Arg93Trp)not specified [RCV004449945]uncertain significance206397713963977139Humanname
597735636CV3594657single nucleotide variantNM_080621.5(SAMD10):c.175C>T (p.Pro59Ser)not specified [RCV004863691]uncertain significance206397732363977323Humanname
597735642CV3594658single nucleotide variantNM_080621.5(SAMD10):c.218C>T (p.Ala73Val)not specified [RCV004863692]uncertain significance206397728063977280Humanname
597735653CV3594660single nucleotide variantNM_080621.5(SAMD10):c.121C>G (p.Leu41Val)not specified [RCV004863694]uncertain significance206397737763977377Humanname
597735658CV3594661single nucleotide variantNM_080621.5(SAMD10):c.217G>A (p.Ala73Thr)not specified [RCV004863695]uncertain significance206397728163977281Humanname
597735663CV3594662single nucleotide variantNM_080621.5(SAMD10):c.134C>T (p.Thr45Met)not specified [RCV004863696]uncertain significance206397736463977364Humanname
598208389CV3906509single nucleotide variantNM_080621.5(SAMD10):c.130C>G (p.His44Asp)not specified [RCV005270239]uncertain significance206397736863977368Humanname
156173962CV2326898single nucleotide variantNM_080621.5(SAMD10):c.602T>C (p.Met201Thr)not specified [RCV004176717]uncertain significance206397551763975517Humanname
329371540CV2432006single nucleotide variantNM_080621.5(SAMD10):c.337C>T (p.Arg113Trp)not specified [RCV004249159]uncertain significance206397707963977079Humanname
329352116CV2452051single nucleotide variantNM_080621.5(SAMD10):c.373A>C (p.Lys125Gln)not specified [RCV004278781]uncertain significance206397704363977043Humanname
405722004CV3320385single nucleotide variantNM_080621.5(SAMD10):c.328G>T (p.Gly110Cys)not specified [RCV004449946]uncertain significance206397708863977088Humanname
405722011CV3320386single nucleotide variantNM_080621.5(SAMD10):c.409G>A (p.Val137Ile)not specified [RCV004449947]uncertain significance206397700763977007Humanname
405722021CV3320387single nucleotide variantNM_080621.5(SAMD10):c.463C>G (p.Leu155Val)not specified [RCV004449948]uncertain significance206397581563975815Humanname
407469185CV3483548single nucleotide variantNM_080621.5(SAMD10):c.400A>T (p.Asn134Tyr)not specified [RCV004661391]uncertain significance206397701663977016Humanname
597735648CV3594659single nucleotide variantNM_080621.5(SAMD10):c.551G>A (p.Arg184His)not specified [RCV004863693]uncertain significance206397572763975727Humanname