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17 records found for search term Acvr2a
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
598204238CV3943023single nucleotide variantNM_001616.5(ACVR2A):c.11C>T (p.Ala4Val)not specified [RCV005314758]uncertain significance2147845163147845163Humanname
329395272CV2458257single nucleotide variantNM_001616.5(ACVR2A):c.281A>G (p.Lys94Arg)not specified [RCV004265912]uncertain significance2147899475147899475Humanname
405723482CV3293187single nucleotide variantNM_001616.5(ACVR2A):c.146C>T (p.Pro49Leu)not specified [RCV004428457]uncertain significance2147896391147896391Humanname
597776968CV3641026single nucleotide variantNM_001616.5(ACVR2A):c.166A>G (p.Lys56Glu)not specified [RCV004898630]uncertain significance2147896411147896411Humanname
156042549CV2261467single nucleotide variantNM_001616.5(ACVR2A):c.781G>A (p.Val261Met)not specified [RCV004130088]uncertain significance2147917391147917391Humanname
156300315CV2306943single nucleotide variantNM_001616.5(ACVR2A):c.995A>C (p.Asn332Thr)not specified [RCV004157462]uncertain significance2147920262147920262Humanname
156350011CV2316123single nucleotide variantNM_001616.5(ACVR2A):c.392C>G (p.Thr131Arg)not specified [RCV004174175]uncertain significance2147899762147899762Humanname
156210541CV2378155single nucleotide variantNM_001616.5(ACVR2A):c.484A>G (p.Arg162Gly)not specified [RCV004233072]uncertain significance2147899854147899854Humanname
401757312CV2675225single nucleotide variantNM_001616.5(ACVR2A):c.667A>G (p.Ile223Val)not specified [RCV004289995]uncertain significance2147915329147915329Humanname
401898649CV2782579single nucleotide variantNM_001616.5(ACVR2A):c.895G>C (p.Gly299Arg)not specified [RCV004359613]uncertain significance2147918525147918525Humanname
598204110CV3942994single nucleotide variantNM_001616.5(ACVR2A):c.323A>G (p.Asn108Ser)not specified [RCV005314734]uncertain significance2147899517147899517Humanname
598204155CV3943004single nucleotide variantNM_001616.5(ACVR2A):c.470C>T (p.Ala157Val)not specified [RCV005314743]uncertain significance2147899840147899840Humanname
156302170CV2241726single nucleotide variantNM_001616.5(ACVR2A):c.1088G>A (p.Arg363Gln)not specified [RCV004106669]uncertain significance2147922983147922983Humanname
401877981CV2760097single nucleotide variantNM_001616.5(ACVR2A):c.1481T>C (p.Ile494Thr)not specified [RCV004345504]uncertain significance2147927213147927213Humanname
405723575CV3293199single nucleotide variantNM_001616.5(ACVR2A):c.1483G>T (p.Val495Leu)not specified [RCV004428469]uncertain significance2147927215147927215Humanname
597777002CV3641035single nucleotide variantNM_001616.5(ACVR2A):c.1063G>A (p.Asp355Asn)not specified [RCV004898639]uncertain significance2147920330147920330Humanname
598204195CV3943014single nucleotide variantNM_001616.5(ACVR2A):c.1303A>C (p.Lys435Gln)not specified [RCV005314751]uncertain significance2147926117147926117Humanname