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Variants search result for Homo sapiens
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17 records found for search term Sertad1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
598226400CV3900538single nucleotide variantNM_013376.4(SERTAD1):c.94G>C (p.Ala32Pro)not specified [RCV005273505]uncertain significance194042345340423453Humanname
598226405CV3900539single nucleotide variantNM_013376.4(SERTAD1):c.95C>T (p.Ala32Val)not specified [RCV005273506]uncertain significance194042345240423452Humanname
401752638CV2707076single nucleotide variantNM_013376.4(SERTAD1):c.248C>T (p.Pro83Leu)not specified [RCV004321660]uncertain significance194042329940423299Humanname
405761530CV3311111single nucleotide variantNM_013376.4(SERTAD1):c.248C>A (p.Pro83His)not specified [RCV004455396]uncertain significance194042329940423299Humanname
407489307CV3473736single nucleotide variantNM_013376.4(SERTAD1):c.251C>T (p.Ala84Val)not specified [RCV004666028]uncertain significance194042329640423296Humanname
597670684CV3598696single nucleotide variantNM_013376.4(SERTAD1):c.197A>C (p.His66Pro)not specified [RCV004856340]uncertain significance194042335040423350Humanname
156053590CV2242985single nucleotide variantNM_013376.4(SERTAD1):c.445G>C (p.Ala149Pro)not specified [RCV004107864]likely benign194042310240423102Humanname
329367496CV2427305single nucleotide variantNM_013376.4(SERTAD1):c.689G>A (p.Arg230Gln)not specified [RCV004248165]uncertain significance194042285840422858Humanname
401744290CV2680934single nucleotide variantNM_013376.4(SERTAD1):c.622C>G (p.Pro208Ala)not specified [RCV004296006]uncertain significance194042292540422925Humanname
401770437CV2711169single nucleotide variantNM_013376.4(SERTAD1):c.667G>A (p.Val223Met)not specified [RCV004310840]uncertain significance194042288040422880Humanname
401730970CV2711596single nucleotide variantNM_013376.4(SERTAD1):c.706C>T (p.Arg236Cys)not specified [RCV004306902]uncertain significance194042284140422841Humanname
405761538CV3311112single nucleotide variantNM_013376.4(SERTAD1):c.382C>A (p.Leu128Met)not specified [RCV004455397]uncertain significance194042316540423165Humanname
405761544CV3311113single nucleotide variantNM_013376.4(SERTAD1):c.529A>T (p.Ile177Phe)not specified [RCV004455398]uncertain significance194042301840423018Humanname
405761552CV3311114single nucleotide variantNM_013376.4(SERTAD1):c.565C>T (p.Pro189Ser)not specified [RCV004455399]uncertain significance194042298240422982Humanname
405761567CV3311116single nucleotide variantNM_013376.4(SERTAD1):c.707G>A (p.Arg236His)not specified [RCV004455401]uncertain significance194042284040422840Humanname
407489311CV3473737single nucleotide variantNM_013376.4(SERTAD1):c.601G>C (p.Gly201Arg)not specified [RCV004666029]uncertain significance194042294640422946Humanname
597670675CV3598695single nucleotide variantNM_013376.4(SERTAD1):c.616G>A (p.Glu206Lys)not specified [RCV004856339]uncertain significance194042293140422931Humanname