Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs137852773
rs137852773
1.000 0.200 2 26214516 missense variant A/T snv 4.0E-06
Trifunctional Protein Deficiency With Myopathy And Neuropathy
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases 0.800 1.000 1 1998 1998
dbSNP: rs137852774
rs137852774
0.925 0.200 2 26214447 missense variant A/G;T snv 4.0E-06; 8.0E-06
Trifunctional Protein Deficiency With Myopathy And Neuropathy
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases 0.800 1.000 1 1998 1998
dbSNP: rs137852769
rs137852769
0.827 0.280 2 26195184 missense variant C/G snv 1.2E-03 1.0E-03
Trifunctional Protein Deficiency With Myopathy And Neuropathy
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases 0.790 1.000 13 1994 2017
dbSNP: rs1057516460
rs1057516460
0.925 0.200 2 26204190 splice acceptor variant GATGCCTGCA/- delins
Trifunctional Protein Deficiency With Myopathy And Neuropathy
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 5 1995 2012
dbSNP: rs1167218743
rs1167218743
0.925 0.200 2 26192309 splice donor variant C/A;G snv 7.0E-06
Trifunctional Protein Deficiency With Myopathy And Neuropathy
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 5 1995 2012
dbSNP: rs1057516417
rs1057516417
0.925 0.200 2 26234216 splice donor variant C/T snv
Trifunctional Protein Deficiency With Myopathy And Neuropathy
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 4 1995 2012
dbSNP: rs781205883
rs781205883
1.000 0.200 2 26236891 frameshift variant GAGAT/- delins 8.0E-06 7.0E-06
Trifunctional Protein Deficiency With Myopathy And Neuropathy
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 4 1999 2012
dbSNP: rs781222705
rs781222705
0.925 0.200 2 26238931 splice region variant T/C snv 5.2E-05
Trifunctional Protein Deficiency With Myopathy And Neuropathy
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 4 1995 2016
dbSNP: rs769580842
rs769580842
0.925 0.200 2 26193668 frameshift variant AT/- del 3.5E-05
Trifunctional Protein Deficiency With Myopathy And Neuropathy
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 3 2002 2003
dbSNP: rs786204607
rs786204607
1.000 0.200 2 26215149 missense variant G/A snv
Trifunctional Protein Deficiency With Myopathy And Neuropathy
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 3 2009 2012
dbSNP: rs137852771
rs137852771
0.925 0.200 2 26194581 stop gained G/A snv 2.4E-05
Trifunctional Protein Deficiency With Myopathy And Neuropathy
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 2 1996 2016
dbSNP: rs779113356
rs779113356
0.925 0.200 2 26192343 frameshift variant A/- delins 4.0E-06
Trifunctional Protein Deficiency With Myopathy And Neuropathy
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 2 1999 2011
dbSNP: rs749848370
rs749848370
1.000 0.200 2 26192311 frameshift variant TAGGAGGCAGCTTCAGACT/- delins 1.2E-05
Trifunctional Protein Deficiency With Myopathy And Neuropathy
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs137852770
rs137852770
0.925 0.200 2 26204150 stop gained G/A snv 7.0E-06
Trifunctional Protein Deficiency With Myopathy And Neuropathy
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases 0.700 0
dbSNP: rs137852775
rs137852775
0.925 0.200 2 26214490 stop gained G/A snv
Trifunctional Protein Deficiency With Myopathy And Neuropathy
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases 0.700 0
dbSNP: rs138966725
rs138966725
1.000 0.200 2 26191498 missense variant G/A;T snv 2.0E-04 1.6E-04
Trifunctional Protein Deficiency With Myopathy And Neuropathy
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases 0.700 0
dbSNP: rs1456890163
rs1456890163
1.000 0.200 2 26244572 frameshift variant -/GCCAATCGCCCGGCAGGCC delins
Trifunctional Protein Deficiency With Myopathy And Neuropathy
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases 0.700 0
dbSNP: rs786205088
rs786205088
0.925 0.200 2 26238933 splice donor variant C/T snv
Trifunctional Protein Deficiency With Myopathy And Neuropathy
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases 0.700 0