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Pathways
Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)


5 records found for search term Arpp19
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156333431CV2335986single nucleotide variantNM_006628.6(ARPP19):c.40C>G (p.Gln14Glu)not specified [RCV004189595]uncertain significance155256885352568853Humanname
598176154CV3905425single nucleotide variantNM_006628.6(ARPP19):c.52G>A (p.Glu18Lys)not specified [RCV005264099]uncertain significance155255721652557216Humanname
597730241CV3583102single nucleotide variantNM_006628.6(ARPP19):c.100G>T (p.Ala34Ser)not specified [RCV004863011]uncertain significance155255716852557168Humanname
598176037CV3905406single nucleotide variantNM_006628.6(ARPP19):c.284C>T (p.Pro95Leu)not specified [RCV005264082]uncertain significance155255198952551989Humanname
598176116CV3905417single nucleotide variantNM_006628.6(ARPP19):c.139G>C (p.Asp47His)not specified [RCV005264093]uncertain significance155255712952557129Humanname