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Pathways
Variants search result for All species
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5 records found for search term Sub1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15165866CV777555single nucleotide variantNM_006713.4(SUB1):c.196-10T>Anot provided [RCV000948697]benign53259895132598951Humanname
15187543CV765102single nucleotide variantNM_006713.4(SUB1):c.144C>T (p.Ala48=)not provided [RCV000931691]likely benign53259163432591634Humanname
156025545CV2242248single nucleotide variantNM_006713.4(SUB1):c.180T>A (p.Asp60Glu)not specified [RCV004111272]uncertain significance53259167032591670Humanname
405781780CV3327267single nucleotide variantNM_006713.4(SUB1):c.161A>G (p.Gln54Arg)not specified [RCV004458788]uncertain significance53259165132591651Humanname
598252078CV3916212single nucleotide variantNM_006713.4(SUB1):c.218G>A (p.Ser73Asn)not specified [RCV005278021]uncertain significance53259898332598983Humanname