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14 records found for search term Fads1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
598223404CV3965665single nucleotide variantNM_013402.7(FADS1):c.11G>A (p.Arg4His)not specified [RCV005341150]uncertain significance116181691961816919Humanname
15122915CV774310single nucleotide variantNM_013402.7(FADS1):c.186G>T (p.Pro62=)not provided [RCV000940761]likely benign116181674461816744Humanname
38467362CV920832single nucleotide variantNM_013402.7(FADS1):c.141T>G (p.Ala47=)not provided [RCV001200346]likely benign116181678961816789Humanname
405724170CV3249597single nucleotide variantNM_013402.7(FADS1):c.83G>A (p.Arg28His)not specified [RCV004378417]uncertain significance116181684761816847Humanname
156343440CV2353464single nucleotide variantNM_013402.7(FADS1):c.116C>G (p.Pro39Arg)not specified [RCV004205918]uncertain significance116181681461816814Humanname
598223412CV3965666single nucleotide variantNM_013402.7(FADS1):c.181G>A (p.Asp61Asn)not specified [RCV005341151]uncertain significance116181674961816749Humanname
155942233CV2229517single nucleotide variantNM_013402.7(FADS1):c.664G>T (p.Val222Leu)not specified [RCV004103058]uncertain significance116181249161812491Humanname
155928398CV2391725single nucleotide variantNM_013402.7(FADS1):c.533G>A (p.Arg178Gln)not specified [RCV004241878]likely benign116181262261812622Humanname
401879256CV2774536single nucleotide variantNM_013402.7(FADS1):c.532C>T (p.Arg178Trp)not specified [RCV004350021]uncertain significance116181262361812623Humanname
597718369CV3671765single nucleotide variantNM_013402.7(FADS1):c.851G>A (p.Arg284His)not specified [RCV004918516]uncertain significance116181081561810815Humanname
598223389CV3965663single nucleotide variantNM_013402.7(FADS1):c.556C>T (p.His186Tyr)not specified [RCV005341148]uncertain significance116181259961812599Humanname
598223397CV3965664single nucleotide variantNM_013402.7(FADS1):c.662C>T (p.Ala221Val)not specified [RCV005341149]uncertain significance116181249361812493Humanname
156184121CV2294853single nucleotide variantNM_013402.7(FADS1):c.1416G>T (p.Gln472His)not specified [RCV004156014]uncertain significance116180283961802839Humanname
407501007CV3435344single nucleotide variantNM_013402.7(FADS1):c.1191G>T (p.Met397Ile)not specified [RCV004623166]uncertain significance116180342061803420Humanname