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10 records found for search term S100a16
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155971421CV2214117single nucleotide variantNM_080388.3(S100A16):c.195C>A (p.Asn65Lys)not specified [RCV004086124]uncertain significance1153607651153607651Humanname
156236327CV2239006single nucleotide variantNM_080388.3(S100A16):c.284A>G (p.His95Arg)not specified [RCV004109891]likely benign1153607562153607562Humanname
156343214CV2364079single nucleotide variantNM_080388.3(S100A16):c.183G>C (p.Lys61Asn)not specified [RCV004221462]uncertain significance1153607663153607663Humanname
156017552CV2370124single nucleotide variantNM_080388.3(S100A16):c.287A>G (p.Glu96Gly)not specified [RCV004211011]uncertain significance1153607559153607559Humanname
405702024CV3310155single nucleotide variantNM_080388.3(S100A16):c.116G>T (p.Arg39Leu)not specified [RCV004447233]uncertain significance1153608036153608036Humanname
405702033CV3310156single nucleotide variantNM_080388.3(S100A16):c.166C>T (p.Arg56Trp)not specified [RCV004447234]uncertain significance1153607680153607680Humanname
405702038CV3310157single nucleotide variantNM_080388.3(S100A16):c.167G>T (p.Arg56Leu)not specified [RCV004447235]uncertain significance1153607679153607679Humanname
405702047CV3310158single nucleotide variantNM_080388.3(S100A16):c.218G>A (p.Arg73His)not specified [RCV004447236]uncertain significance1153607628153607628Humanname
405702057CV3310159single nucleotide variantNM_080388.3(S100A16):c.281T>A (p.Ile94Asn)not specified [RCV004447237]uncertain significance1153607565153607565Humanname
597734690CV3597884single nucleotide variantNM_080388.3(S100A16):c.123G>A (p.Met41Ile)not specified [RCV004863525]uncertain significance1153608029153608029Humanname