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Variants search result for Homo sapiens
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21 records found for search term Phospho2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156037240CV2250168single nucleotide variantNM_001008489.4(PHOSPHO2):c.5A>G (p.Lys2Arg)not specified [RCV004116970]uncertain significance2169700976169700976Humanname
401723847CV2684888single nucleotide variantNM_001008489.4(PHOSPHO2):c.50A>G (p.Asn17Ser)not specified [RCV004296393]uncertain significance2169701021169701021Humanname
401729448CV2733059single nucleotide variantNM_001008489.4(PHOSPHO2):c.37A>G (p.Ile13Val)not specified [RCV004331228]uncertain significance2169701008169701008Humanname
156156684CV2359866single nucleotide variantNM_001008489.4(PHOSPHO2):c.224C>A (p.Thr75Asn)not specified [RCV004212717]uncertain significance2169701195169701195Humanname
329370319CV2435545single nucleotide variantNM_001008489.4(PHOSPHO2):c.232A>G (p.Met78Val)not specified [RCV004254802]uncertain significance2169701203169701203Humanname
329355335CV2449329single nucleotide variantNM_001008489.4(PHOSPHO2):c.295G>T (p.Asp99Tyr)not specified [RCV004257458]uncertain significance2169701266169701266Humanname
597679825CV3569174single nucleotide variantNM_001008489.4(PHOSPHO2):c.284T>C (p.Ile95Thr)not specified [RCV004837202]uncertain significance2169701255169701255Humanname
598249715CV3996771single nucleotide variantNM_001008489.4(PHOSPHO2):c.118C>G (p.Arg40Gly)not specified [RCV005384500]uncertain significance2169701089169701089Humanname
8625198CV80317single nucleotide variantNM_001008489.3(PHOSPHO2):c.175G>A (p.Gly59Ser)Malignant melanoma [RCV000060394]not provided2169701146169701146Humanname
156253657CV2264596single nucleotide variantNM_001008489.4(PHOSPHO2):c.305C>T (p.Ser102Leu)not specified [RCV004132607]uncertain significance2169701276169701276Humanname
155929081CV2277933single nucleotide variantNM_001008489.4(PHOSPHO2):c.490C>G (p.Gln164Glu)not specified [RCV004141185]uncertain significance2169701461169701461Humanname
156044696CV2305961single nucleotide variantNM_001008489.4(PHOSPHO2):c.711T>G (p.Phe237Leu)not specified [RCV004169523]uncertain significance2169701682169701682Humanname
156223227CV2394869single nucleotide variantNM_001008489.4(PHOSPHO2):c.338G>A (p.Ser113Asn)not specified [RCV004234527]likely benign2169701309169701309Humanname
401755647CV2682541single nucleotide variantNM_001008489.4(PHOSPHO2):c.715A>G (p.Ile239Val)not specified [RCV004290554]uncertain significance2169701686169701686Humanname
401754751CV2716004single nucleotide variantNM_001008489.4(PHOSPHO2):c.530T>C (p.Ile177Thr)not specified [RCV004323263]uncertain significance2169701501169701501Humanname
597679840CV3569171single nucleotide variantNM_001008489.4(PHOSPHO2):c.638A>C (p.Gln213Pro)not specified [RCV004837200]uncertain significance2169701609169701609Humanname
597679833CV3569172single nucleotide variantNM_001008489.4(PHOSPHO2):c.644T>A (p.Leu215His)not specified [RCV004837201]uncertain significance2169701615169701615Humanname
597767108CV3569173single nucleotide variantNM_001008489.4(PHOSPHO2):c.605A>T (p.Tyr202Phe)not specified [RCV004850401]uncertain significance2169701576169701576Humanname
597679815CV3569175single nucleotide variantNM_001008489.4(PHOSPHO2):c.313A>T (p.Ile105Leu)not specified [RCV004837203]uncertain significance2169701284169701284Humanname
598249700CV3996769single nucleotide variantNM_001008489.4(PHOSPHO2):c.361G>A (p.Val121Met)not specified [RCV005384498]uncertain significance2169701332169701332Humanname
598249707CV3996770single nucleotide variantNM_001008489.4(PHOSPHO2):c.648G>C (p.Glu216Asp)not specified [RCV005384499]uncertain significance2169701619169701619Humanname