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Pathways
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5 records found for search term Gpr146
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401921106CV2828174single nucleotide variantNM_001303473.2(GPR146):c.222G>C (p.Leu74=)not provided [RCV003432196]likely benign710577371057737Humanname
15171949CV699727single nucleotide variantNM_001303473.2(GPR146):c.123C>T (p.Gly41=)not provided [RCV000949927]benign710576381057638Humanname
15186263CV699728single nucleotide variantNM_001303473.2(GPR146):c.444C>T (p.Cys148=)not provided [RCV000953231]benign710579591057959Humanname
401908620CV2828175single nucleotide variantNM_001303473.2(GPR146):c.404G>A (p.Arg135Gln)not provided [RCV003423494]likely benign710579191057919Humanname
401908622CV2828176single nucleotide variantNM_001303473.2(GPR146):c.662A>G (p.Asp221Gly)not provided [RCV003423495]likely benign710581771058177Humanname