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Variants search result for Homo sapiens
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17 records found for search term Fkbp3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156161105CV2236420single nucleotide variantNM_002013.4(FKBP3):c.22C>T (p.Arg8Trp)not specified [RCV004108095]uncertain significance144513443545134435Humanname
156064637CV2272440single nucleotide variantNM_002013.4(FKBP3):c.73A>G (p.Ile25Val)not specified [RCV004133360]uncertain significance144513438445134384Humanname
156239491CV2285975single nucleotide variantNM_002013.4(FKBP3):c.268C>T (p.Leu90Phe)not specified [RCV004143890]uncertain significance144512984445129844Humanname
156202794CV2313249single nucleotide variantNM_002013.4(FKBP3):c.194A>G (p.His65Arg)not specified [RCV004161500]uncertain significance144513071545130715Humanname
156264414CV2388951single nucleotide variantNM_002013.4(FKBP3):c.232A>G (p.Ile78Val)not specified [RCV004241952]likely benign144512988045129880Humanname
329386315CV2455848single nucleotide variantNM_002013.4(FKBP3):c.245C>T (p.Ser82Phe)not specified [RCV004279130]uncertain significance144512986745129867Humanname
405780134CV3260695single nucleotide variantNM_002013.4(FKBP3):c.220G>C (p.Gly74Arg)not specified [RCV004386630]uncertain significance144512989245129892Humanname
597699289CV3666238single nucleotide variantNM_002013.4(FKBP3):c.170A>G (p.Asp57Gly)not specified [RCV004916227]uncertain significance144513073945130739Humanname
597699315CV3666241single nucleotide variantNM_002013.4(FKBP3):c.139A>G (p.Ile47Val)not specified [RCV004916230]uncertain significance144513077045130770Humanname
155964562CV2330463single nucleotide variantNM_002013.4(FKBP3):c.394C>T (p.His132Tyr)not specified [RCV004181033]uncertain significance144512154545121545Humanname
329370230CV2461640single nucleotide variantNM_002013.4(FKBP3):c.514A>T (p.Ile172Phe)not specified [RCV004269810]uncertain significance144512089545120895Humanname
401865582CV2755560single nucleotide variantNM_002013.4(FKBP3):c.566G>A (p.Arg189Gln)not specified [RCV004340139]uncertain significance144511808245118082Humanname
405780146CV3260697single nucleotide variantNM_002013.4(FKBP3):c.559A>G (p.Lys187Glu)not specified [RCV004386632]uncertain significance144511808945118089Humanname
407502811CV3435950single nucleotide variantNM_002013.4(FKBP3):c.306G>C (p.Glu102Asp)not specified [RCV004623594]uncertain significance144512980645129806Humanname
407479119CV3435951single nucleotide variantNM_002013.4(FKBP3):c.639A>C (p.Lys213Asn)not specified [RCV004623595]uncertain significance144511623445116234Humanname
597699297CV3666239single nucleotide variantNM_002013.4(FKBP3):c.650A>C (p.Glu217Ala)not specified [RCV004916228]uncertain significance144511622345116223Humanname
597699307CV3666240single nucleotide variantNM_002013.4(FKBP3):c.511G>T (p.Val171Phe)not specified [RCV004916229]uncertain significance144512089845120898Humanname