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Variants search result for Homo sapiens
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21 records found for search term Caly
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156064397CV2287135single nucleotide variantNM_015722.4(CALY):c.20G>T (p.Ser7Ile)not specified [RCV004145001]uncertain significance10133328970133328970Humanname
405766953CV3302597single nucleotide variantNM_015722.4(CALY):c.17G>A (p.Cys6Tyr)not specified [RCV004434611]uncertain significance10133328973133328973Humanname
597763873CV3647398single nucleotide variantNM_015722.4(CALY):c.13G>A (p.Gly5Ser)not specified [RCV004895475]uncertain significance10133328977133328977Humanname
401928729CV2806343single nucleotide variantNM_015722.4(CALY):c.369C>T (p.Ile123=)not provided [RCV003389971]likely benign10133326112133326112Humanname
405766974CV3302600single nucleotide variantNM_015722.4(CALY):c.57G>C (p.Gln19His)not specified [RCV004434614]uncertain significance10133328933133328933Humanname
407476012CV3424456single nucleotide variantNM_015722.4(CALY):c.67G>C (p.Ala23Pro)not specified [RCV004600622]uncertain significance10133328923133328923Humanname
156378275CV2207675single nucleotide variantNM_015722.4(CALY):c.136G>A (p.Val46Met)not specified [RCV004084130]uncertain significance10133328015133328015Humanname
156160502CV2272519single nucleotide variantNM_015722.4(CALY):c.256G>T (p.Ala86Ser)not specified [RCV004133421]uncertain significance10133326982133326982Humanname
401720577CV2673384single nucleotide variantNM_015722.4(CALY):c.232G>A (p.Glu78Lys)not specified [RCV004288363]uncertain significance10133327919133327919Humanname
405766960CV3302598single nucleotide variantNM_015722.4(CALY):c.242G>A (p.Arg81His)not specified [RCV004434612]uncertain significance10133327909133327909Humanname
597763877CV3647399single nucleotide variantNM_015722.4(CALY):c.292T>C (p.Cys98Arg)not specified [RCV004895476]uncertain significance10133326946133326946Humanname
598203806CV3942932single nucleotide variantNM_015722.4(CALY):c.295G>A (p.Val99Met)not specified [RCV005314687]uncertain significance10133326943133326943Humanname
598203820CV3942934single nucleotide variantNM_015722.4(CALY):c.142A>T (p.Ile48Phe)not specified [RCV005314689]uncertain significance10133328009133328009Humanname
156330790CV2224318single nucleotide variantNM_015722.4(CALY):c.429C>A (p.Ser143Arg)not specified [RCV004096136]uncertain significance10133326052133326052Humanname
156078836CV2341214single nucleotide variantNM_015722.4(CALY):c.575C>G (p.Pro192Arg)not specified [RCV004186630]uncertain significance10133325906133325906Humanname
156050515CV2367516single nucleotide variantNM_015722.4(CALY):c.305T>C (p.Met102Thr)not specified [RCV004211451]uncertain significance10133326933133326933Humanname
401735264CV2687534single nucleotide variantNM_015722.4(CALY):c.505T>A (p.Tyr169Asn)not specified [RCV004300764]uncertain significance10133325976133325976Humanname
405766980CV3302601single nucleotide variantNM_015722.4(CALY):c.584C>A (p.Pro195Gln)not specified [RCV004434615]uncertain significance10133325897133325897Humanname
405766986CV3302602single nucleotide variantNM_015722.4(CALY):c.613C>T (p.Arg205Trp)not specified [RCV004434616]uncertain significance10133325868133325868Humanname
597763869CV3647397single nucleotide variantNM_015722.4(CALY):c.462C>A (p.Ser154Arg)not specified [RCV004895474]uncertain significance10133326019133326019Humanname
598203814CV3942933single nucleotide variantNM_015722.4(CALY):c.444C>G (p.Ile148Met)not specified [RCV005314688]uncertain significance10133326037133326037Humanname