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22 records found for search term Spc25
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407511104CV3481614single nucleotide variantNM_020675.4(SPC25):c.19G>A (p.Ala7Thr)not specified [RCV004672930]uncertain significance2168889501168889501Humanname
156034268CV2275208single nucleotide variantNM_020675.4(SPC25):c.30T>A (p.Asp10Glu)not specified [RCV004136999]uncertain significance2168889490168889490Humanname
405716650CV3326645single nucleotide variantNM_020675.4(SPC25):c.49T>A (p.Trp17Arg)not specified [RCV004462596]uncertain significance2168889471168889471Humanname
401891716CV2779344single nucleotide variantNM_020675.4(SPC25):c.190T>C (p.Tyr64His)not specified [RCV004351004]uncertain significance2168889235168889235Humanname
597767931CV3608106single nucleotide variantNM_020675.4(SPC25):c.163G>A (p.Glu55Lys)not specified [RCV004870932]uncertain significance2168889262168889262Humanname
598238945CV3919041single nucleotide variantNM_020675.4(SPC25):c.160G>A (p.Glu54Lys)not specified [RCV005275920]uncertain significance2168889265168889265Humanname
8629958CV85105single nucleotide variantNM_020675.3(SPC25):c.199C>T (p.Gln67Ter)Malignant melanoma [RCV000065187]not provided2168889226168889226Humanname
156385549CV2227957single nucleotide variantNM_020675.4(SPC25):c.457A>C (p.Lys153Gln)not specified [RCV004096207]uncertain significance2168873678168873678Humanname
156063434CV2240155single nucleotide variantNM_020675.4(SPC25):c.504C>A (p.Ser168Arg)not specified [RCV004110914]uncertain significance2168873631168873631Humanname
156276875CV2255842single nucleotide variantNM_020675.4(SPC25):c.505C>A (p.Pro169Thr)not specified [RCV004122003]uncertain significance2168873630168873630Humanname
156335733CV2360531single nucleotide variantNM_020675.4(SPC25):c.556G>C (p.Asp186His)not specified [RCV004211291]uncertain significance2168871550168871550Humanname
156077729CV2375129single nucleotide variantNM_020675.4(SPC25):c.368C>T (p.Ala123Val)not specified [RCV004230173]uncertain significance2168876155168876155Humanname
401753102CV2674779single nucleotide variantNM_020675.4(SPC25):c.341A>G (p.Lys114Arg)not specified [RCV004294058]uncertain significance2168877243168877243Humanname
405716634CV3326643single nucleotide variantNM_020675.4(SPC25):c.349A>G (p.Ile117Val)not specified [RCV004462594]uncertain significance2168876174168876174Humanname
405716642CV3326644single nucleotide variantNM_020675.4(SPC25):c.388A>G (p.Arg130Gly)not specified [RCV004462595]uncertain significance2168876135168876135Humanname
405716659CV3326646single nucleotide variantNM_020675.4(SPC25):c.574G>C (p.Glu192Gln)not specified [RCV004462597]uncertain significance2168871532168871532Humanname
405716665CV3326647single nucleotide variantNM_020675.4(SPC25):c.601G>A (p.Val201Ile)not specified [RCV004462598]uncertain significance2168871505168871505Humanname
405716674CV3326648single nucleotide variantNM_020675.4(SPC25):c.662C>T (p.Thr221Met)not specified [RCV004462599]likely benign2168871444168871444Humanname
407511013CV3481615single nucleotide variantNM_020675.4(SPC25):c.332C>G (p.Ser111Cys)not specified [RCV004672931]uncertain significance2168877252168877252Humanname
597742638CV3608107single nucleotide variantNM_020675.4(SPC25):c.581T>C (p.Leu194Pro)not specified [RCV004865121]uncertain significance2168871525168871525Humanname
598262539CV3919042single nucleotide variantNM_020675.4(SPC25):c.587A>G (p.Glu196Gly)not specified [RCV005280211]uncertain significance2168871519168871519Humanname
598262542CV3919043single nucleotide variantNM_020675.4(SPC25):c.390G>T (p.Arg130Ser)not specified [RCV005280212]uncertain significance2168876133168876133Humanname