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Pathways
Variants search result for All species
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8 records found for search term S100a4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15155756CV706705single nucleotide variantNM_002961.3(S100A4):c.60G>A (p.Ser20=)not provided [RCV000968982]benign1153544735153544735Humanname
15098153CV696120single nucleotide variantNM_002961.3(S100A4):c.234C>T (p.Phe78=)not provided [RCV000958489]benign1153543831153543831Humanname
15183413CV696121single nucleotide variantNM_002961.3(S100A4):c.183C>T (p.Asn61=)not provided [RCV000952456]benign1153543882153543882Humanname
15196231CV745700single nucleotide variantNM_002961.3(S100A4):c.204C>T (p.Asn68=)not provided [RCV000911639]benign1153543861153543861Humanname
155997410CV2250551single nucleotide variantNM_002961.3(S100A4):c.139G>A (p.Gly47Arg)not specified [RCV004127409]uncertain significance1153544656153544656Humanname
156111602CV2353354single nucleotide variantNM_002961.3(S100A4):c.205G>A (p.Glu69Lys)not specified [RCV004205817]uncertain significance1153543860153543860Humanname
597734695CV3597885single nucleotide variantNM_002961.3(S100A4):c.119G>A (p.Arg40Gln)not specified [RCV004863526]uncertain significance1153544676153544676Humanname
597734700CV3597887single nucleotide variantNM_002961.3(S100A4):c.250A>T (p.Met84Leu)not specified [RCV004863527]uncertain significance1153543815153543815Humanname