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Variants search result for Homo sapiens
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25 records found for search term Vta1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401880944CV2787737single nucleotide variantNM_016485.5(VTA1):c.13G>A (p.Ala5Thr)not specified [RCV004356650]uncertain significance6142147300142147300Humanname
597687752CV3626818single nucleotide variantNM_016485.5(VTA1):c.11T>A (p.Leu4His)not specified [RCV004884292]uncertain significance6142147298142147298Humanname
405281819CV3224415single nucleotide variantNM_016485.5(VTA1):c.52C>T (p.Gln18Ter)not specified [RCV003988798]likely pathogenic6142147339142147339Humanname
598256151CV3926195single nucleotide variantNM_016485.5(VTA1):c.68C>T (p.Thr23Met)not specified [RCV005299559]uncertain significance6142147355142147355Humanname
155915312CV2243732single nucleotide variantNM_016485.5(VTA1):c.160C>T (p.Pro54Ser)not specified [RCV004114431]uncertain significance6142166275142166275Humanname
155989451CV2244253single nucleotide variantNM_016485.5(VTA1):c.149A>G (p.Asp50Gly)not specified [RCV004100250]uncertain significance6142166264142166264Humanname
156176186CV2254711single nucleotide variantNM_016485.5(VTA1):c.170G>A (p.Arg57His)not specified [RCV004115188]uncertain significance6142166285142166285Humanname
156248056CV2357105single nucleotide variantNM_016485.5(VTA1):c.169C>T (p.Arg57Cys)not specified [RCV004206903]uncertain significance6142166284142166284Humanname
401778434CV2714723single nucleotide variantNM_016485.5(VTA1):c.218A>G (p.Gln73Arg)not specified [RCV004320295]uncertain significance6142169560142169560Humanname
155994318CV2286402single nucleotide variantNM_016485.5(VTA1):c.908C>T (p.Thr303Met)not specified [RCV004139925]uncertain significance6142218627142218627Humanname
156274126CV2320234single nucleotide variantNM_016485.5(VTA1):c.800A>T (p.Glu267Val)not specified [RCV004169852]uncertain significance6142218519142218519Humanname
156133345CV2350291single nucleotide variantNM_016485.5(VTA1):c.317G>A (p.Arg106His)not specified [RCV004202245]uncertain significance6142169659142169659Humanname
156092539CV2389595single nucleotide variantNM_016485.5(VTA1):c.458A>G (p.His153Arg)not specified [RCV004243659]uncertain significance6142189472142189472Humanname
329375362CV2468543single nucleotide variantNM_016485.5(VTA1):c.754G>T (p.Ala252Ser)not specified [RCV004278115]uncertain significance6142204041142204041Humanname
329387514CV2470778single nucleotide variantNM_016485.5(VTA1):c.382A>G (p.Ile128Val)not specified [RCV004276005]uncertain significance6142170392142170392Humanname
401741978CV2721827single nucleotide variantNM_016485.5(VTA1):c.560C>G (p.Pro187Arg)not specified [RCV004326343]uncertain significance6142198478142198478Humanname
405663817CV3338541single nucleotide variantNM_016485.5(VTA1):c.364A>C (p.Ser122Arg)not specified [RCV004485071]uncertain significance6142170374142170374Humanname
405663942CV3338542single nucleotide variantNM_016485.5(VTA1):c.716T>C (p.Ile239Thr)not specified [RCV004485072]uncertain significance6142204003142204003Humanname
405663947CV3338543single nucleotide variantNM_016485.5(VTA1):c.754G>A (p.Ala252Thr)not specified [RCV004485073]uncertain significance6142204041142204041Humanname
405663954CV3338544single nucleotide variantNM_016485.5(VTA1):c.787C>T (p.Arg263Cys)not specified [RCV004485074]uncertain significance6142218506142218506Humanname
407450560CV3491541single nucleotide variantNM_016485.5(VTA1):c.541G>A (p.Ala181Thr)not specified [RCV004683344]uncertain significance6142198459142198459Humanname
597687733CV3626816single nucleotide variantNM_016485.5(VTA1):c.716T>A (p.Ile239Asn)not specified [RCV004884290]uncertain significance6142204003142204003Humanname
597687742CV3626817single nucleotide variantNM_016485.5(VTA1):c.652G>A (p.Ala218Thr)not specified [RCV004884291]uncertain significance6142198570142198570Humanname
598218090CV3926196single nucleotide variantNM_016485.5(VTA1):c.350C>G (p.Ser117Cys)not specified [RCV005293128]uncertain significance6142170360142170360Humanname
598256155CV3926197single nucleotide variantNM_016485.5(VTA1):c.419A>G (p.Lys140Arg)not specified [RCV005299560]uncertain significance6142189433142189433Humanname