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Variants search result for Homo sapiens
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9 records found for search term Ndfip1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156300122CV2248764single nucleotide variantNM_030571.4(NDFIP1):c.29C>T (p.Ala10Val)not specified [RCV004121919]uncertain significance5142109003142109003Humanname
597668240CV3558901single nucleotide variantNM_030571.4(NDFIP1):c.51C>G (p.Ser17Arg)not specified [RCV004829429]uncertain significance5142109025142109025Humanname
15154579CV721270single nucleotide variantNM_030571.4(NDFIP1):c.525T>C (p.Asp175=)not provided [RCV000880244]benign5142140592142140592Humanname
329380326CV2444329single nucleotide variantNM_030571.4(NDFIP1):c.148G>A (p.Ala50Thr)not specified [RCV004263084]uncertain significance5142131892142131892Humanname
407525772CV3454608single nucleotide variantNM_030571.4(NDFIP1):c.283G>A (p.Asp95Asn)not specified [RCV004654596]uncertain significance5142135730142135730Humanname
155970532CV2309193single nucleotide variantNM_030571.4(NDFIP1):c.608G>T (p.Arg203Leu)not specified [RCV004171539]uncertain significance5142144616142144616Humanname
156052665CV2320320single nucleotide variantNM_030571.4(NDFIP1):c.430G>T (p.Ala144Ser)not specified [RCV004178482]uncertain significance5142137793142137793Humanname
598230392CV4003963single nucleotide variantNM_030571.4(NDFIP1):c.559T>G (p.Leu187Val)not specified [RCV005381184]uncertain significance5142140626142140626Humanname
8631459CV86663single nucleotide variantNM_030571.3(NDFIP1):c.635T>A (p.Leu212His)Malignant melanoma [RCV000066754]not provided5142144643142144643Humanname