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Pathways
Variants search result for All species
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16 records found for search term Actr1a
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407492182CV3428710single nucleotide variantNM_005736.4(ACTR1A):c.114T>C (p.Tyr38=)not specified [RCV004604901]likely benign10102489138102489138Humanname
156042249CV2310956single nucleotide variantNM_005736.4(ACTR1A):c.281A>G (p.Tyr94Cys)not specified [RCV004163990]uncertain significance10102488184102488184Humanname
597775304CV3643912single nucleotide variantNM_005736.4(ACTR1A):c.133G>A (p.Val45Ile)not specified [RCV004898206]uncertain significance10102489119102489119Humanname
597775308CV3643915single nucleotide variantNM_005736.4(ACTR1A):c.238G>A (p.Val80Ile)not specified [RCV004898207]uncertain significance10102488227102488227Humanname
597775393CV3643944single nucleotide variantNM_005736.4(ACTR1A):c.209C>T (p.Ser70Leu)not specified [RCV004898227]uncertain significance10102488256102488256Humanname
8633469CV88684single nucleotide variantNM_005736.3(ACTR1A):c.1017C>T (p.Ser339=)Malignant melanoma [RCV000068777]not provided10102481143102481143Humanname
156369956CV2263448single nucleotide variantNM_005736.4(ACTR1A):c.590A>G (p.Tyr197Cys)not specified [RCV004133694]uncertain significance10102484227102484227Humanname
156207258CV2298028single nucleotide variantNM_005736.4(ACTR1A):c.587T>A (p.Leu196His)not specified [RCV004157925]uncertain significance10102484230102484230Humanname
156106468CV2307641single nucleotide variantNM_005736.4(ACTR1A):c.924A>T (p.Lys308Asn)not specified [RCV004168059]uncertain significance10102482002102482002Humanname
405761551CV3300215single nucleotide variantNM_005736.4(ACTR1A):c.803T>C (p.Ile268Thr)not specified [RCV004433732]uncertain significance10102482123102482123Humanname
407492139CV3428700single nucleotide variantNM_005736.4(ACTR1A):c.574C>T (p.Arg192Cys)not specified [RCV004604891]uncertain significance10102484243102484243Humanname
597775338CV3643924single nucleotide variantNM_005736.4(ACTR1A):c.800T>C (p.Leu267Ser)not specified [RCV004898214]uncertain significance10102482126102482126Humanname
597775371CV3643935single nucleotide variantNM_005736.4(ACTR1A):c.380T>G (p.Val127Gly)not specified [RCV004898222]uncertain significance10102485669102485669Humanname
598202275CV3946551single nucleotide variantNM_005736.4(ACTR1A):c.541A>G (p.Met181Val)not specified [RCV005314419]uncertain significance10102484276102484276Humanname
598202307CV3946560single nucleotide variantNM_005736.4(ACTR1A):c.568G>A (p.Val190Ile)not specified [RCV005314426]uncertain significance10102484249102484249Humanname
598202346CV3946571single nucleotide variantNM_005736.4(ACTR1A):c.698C>T (p.Thr233Met)not specified [RCV005314434]uncertain significance10102483063102483063Humanname