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


12 records found for search term Krtcap2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156083362CV2293037single nucleotide variantNM_173852.4(KRTCAP2):c.-30G>Anot specified [RCV004148509]uncertain significance1155173254155173254Humanname
155968222CV2391433single nucleotide variantNM_173852.4(KRTCAP2):c.-72A>Gnot specified [RCV004239828]uncertain significance1155173296155173296Humanname
401748784CV2708347single nucleotide variantNM_173852.4(KRTCAP2):c.-66A>Gnot specified [RCV004313467]uncertain significance1155173290155173290Humanname
405808276CV3266116single nucleotide variantNM_173852.4(KRTCAP2):c.-35C>Tnot specified [RCV004406998]uncertain significance1155173259155173259Humanname
405808278CV3266117single nucleotide variantNM_173852.4(KRTCAP2):c.-27G>Anot specified [RCV004406999]likely benign1155173251155173251Humanname
407480708CV3455963single nucleotide variantNM_173852.4(KRTCAP2):c.10G>A (p.Gly4Ser)not specified [RCV004639785]uncertain significance1155172887155172887Humanname
401888252CV2788201single nucleotide variantNM_173852.4(KRTCAP2):c.197G>A (p.Gly66Glu)not specified [RCV004352814]uncertain significance1155172591155172591Humanname
598196601CV3991380single nucleotide variantNM_173852.4(KRTCAP2):c.144C>A (p.Phe48Leu)not specified [RCV005355209]uncertain significance1155172753155172753Humanname
329380485CV2444413single nucleotide variantNM_173852.4(KRTCAP2):c.373C>T (p.Pro125Ser)not specified [RCV004263155]uncertain significance1155169478155169478Humanname
329396229CV2462445single nucleotide variantNM_173852.4(KRTCAP2):c.326A>G (p.Asn109Ser)not specified [RCV004276636]uncertain significance1155169525155169525Humanname
405808274CV3266115single nucleotide variantNM_173852.4(KRTCAP2):c.307G>T (p.Val103Phe)not specified [RCV004406997]uncertain significance1155169544155169544Humanname
598222431CV3991379single nucleotide variantNM_173852.4(KRTCAP2):c.362C>G (p.Pro121Arg)not specified [RCV005360987]uncertain significance1155169489155169489Humanname