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Variants search result for Homo sapiens
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24 records found for search term Mospd3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597660636CV3563949single nucleotide variantNM_023948.5(MOSPD3):c.5G>A (p.Arg2His)not specified [RCV004828405]uncertain significance7100612796100612796Humanname
401746083CV2694789single nucleotide variantNM_023948.5(MOSPD3):c.13G>A (p.Ala5Thr)not specified [RCV004298872]uncertain significance7100612804100612804Humanname
156050305CV2271868single nucleotide variantNM_023948.5(MOSPD3):c.50C>G (p.Pro17Arg)not specified [RCV004130685]uncertain significance7100612841100612841Humanname
156256429CV2277579single nucleotide variantNM_023948.5(MOSPD3):c.40C>G (p.Pro14Ala)not specified [RCV004145263]uncertain significance7100612831100612831Humanname
155918540CV2333022single nucleotide variantNM_023948.5(MOSPD3):c.79C>A (p.Pro27Thr)not specified [RCV004194321]uncertain significance7100612870100612870Humanname
401886630CV2771349single nucleotide variantNM_023948.5(MOSPD3):c.65G>A (p.Arg22Gln)not specified [RCV004348110]uncertain significance7100612856100612856Humanname
156169723CV2315476single nucleotide variantNM_023948.5(MOSPD3):c.173A>G (p.Tyr58Cys)not specified [RCV004167423]uncertain significance7100612964100612964Humanname
329368735CV2450397single nucleotide variantNM_023948.5(MOSPD3):c.118G>A (p.Asp40Asn)not specified [RCV004265330]uncertain significance7100612909100612909Humanname
401783940CV2720880single nucleotide variantNM_023948.5(MOSPD3):c.233C>T (p.Thr78Met)not specified [RCV004328239]uncertain significance7100613221100613221Humanname
407496064CV3453906single nucleotide variantNM_023948.5(MOSPD3):c.187A>G (p.Thr63Ala)not specified [RCV004643372]likely benign7100612978100612978Humanname
597660642CV3563950single nucleotide variantNM_023948.5(MOSPD3):c.280A>G (p.Ile94Val)not specified [RCV004828406]uncertain significance7100613268100613268Humanname
597660652CV3563953single nucleotide variantNM_023948.5(MOSPD3):c.100G>A (p.Val34Ile)not specified [RCV004828407]uncertain significance7100612891100612891Humanname
156278918CV2297555single nucleotide variantNM_023948.5(MOSPD3):c.535A>G (p.Ser179Gly)not specified [RCV004155262]uncertain significance7100614890100614890Humanname
156344097CV2384667single nucleotide variantNM_023948.5(MOSPD3):c.331C>A (p.Arg111Ser)not specified [RCV004232443]uncertain significance7100613526100613526Humanname
156113157CV2397019single nucleotide variantNM_023948.5(MOSPD3):c.458G>A (p.Arg153His)not specified [RCV004236536]likely benign7100613653100613653Humanname
405723660CV3358984single nucleotide variantNM_023948.5(MOSPD3):c.332G>A (p.Arg111His)not specified [RCV004495488]uncertain significance7100613527100613527Humanname
405723643CV3358986single nucleotide variantNM_023948.5(MOSPD3):c.340A>G (p.Ile114Val)not specified [RCV004495490]uncertain significance7100613535100613535Humanname
405723323CV3358995single nucleotide variantNM_023948.5(MOSPD3):c.701G>A (p.Arg234Gln)not specified [RCV004495499]uncertain significance7100615176100615176Humanname
407496061CV3453905single nucleotide variantNM_023948.5(MOSPD3):c.491C>T (p.Thr164Met)not specified [RCV004643371]uncertain significance7100613686100613686Humanname
597637130CV3563946single nucleotide variantNM_023948.5(MOSPD3):c.700C>T (p.Arg234Trp)not specified [RCV004824689]uncertain significance7100615175100615175Humanname
597660628CV3563947single nucleotide variantNM_023948.5(MOSPD3):c.424C>T (p.Leu142Phe)not specified [RCV004828404]uncertain significance7100613619100613619Humanname
597637134CV3563948single nucleotide variantNM_023948.5(MOSPD3):c.317A>G (p.Tyr106Cys)not specified [RCV004824690]uncertain significance7100613512100613512Humanname
597637138CV3563951single nucleotide variantNM_023948.5(MOSPD3):c.610G>A (p.Gly204Ser)not specified [RCV004824691]likely benign7100614965100614965Humanname
8632225CV87431single nucleotide variantNM_001040097.1(MOSPD3):c.457C>T (p.Arg153Cys)Malignant melanoma [RCV000067522]not provided7100613652100613652Humanname