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Variants search result for Homo sapiens
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11 records found for search term Psma4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597749741CV3591994single nucleotide variantNM_002789.6(PSMA4):c.504C>T (p.Ser168=)not specified [RCV004846290]likely benign157854576178545761Humanname
15104711CV703353single nucleotide variantNM_002789.6(PSMA4):c.339G>A (p.Ala113=)not provided [RCV000959739]benign157854492078544920Humanname
156083465CV2289594single nucleotide variantNM_002789.6(PSMA4):c.278T>G (p.Ile93Ser)not specified [RCV004148519]uncertain significance157854425878544258Humanname
155991087CV2281036single nucleotide variantNM_002789.6(PSMA4):c.724G>A (p.Glu242Lys)not specified [RCV004145525]uncertain significance157854888278548882Humanname
156044673CV2308019single nucleotide variantNM_002789.6(PSMA4):c.503G>A (p.Ser168Asn)not specified [RCV004170447]uncertain significance157854576078545760Humanname
329374946CV2470841single nucleotide variantNM_002789.6(PSMA4):c.574T>G (p.Leu192Val)not specified [RCV004276050]uncertain significance157854664178546641Humanname
401770462CV2685726single nucleotide variantNM_002789.6(PSMA4):c.715A>C (p.Lys239Gln)not specified [RCV004294723]uncertain significance157854887378548873Humanname
405661842CV3378483single nucleotide variantNM_002789.6(PSMA4):c.698T>C (p.Val233Ala)not specified [RCV004513257]uncertain significance157854885678548856Humanname
597749736CV3591993single nucleotide variantNM_002789.6(PSMA4):c.505G>A (p.Ala169Thr)not specified [RCV004846289]uncertain significance157854576278545762Humanname
597749746CV3591995single nucleotide variantNM_002789.6(PSMA4):c.569T>C (p.Leu190Pro)not specified [RCV004846291]uncertain significance157854663678546636Humanname
598170583CV3898156single nucleotide variantNM_002789.6(PSMA4):c.490A>G (p.Ile164Val)not specified [RCV005263139]uncertain significance157854574778545747Humanname