ABCA1 p.His1600Arg

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PMID: 22959828 [PubMed] Fasano T et al: "Novel mutations of ABCA1 transporter in patients with Tangier disease and familial HDL deficiency."
No. Sentence Comment
3 One patient was compound heterozygous for a nucleotide insertion (c.1758_1759insG), resulting in a truncated protein and for a nucleotide substitution c.4799A>G, resulting in a missense mutation (p.H1600R).
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ABCA1 p.His1600Arg 22959828:3:198
status: NEW
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134 Mo-2 33y (M) TD 2.8 1.2 3.2 0.14 na b0.3 [c.1758_1759insG], p.R587Afs*43+[c.4799A>G], p.H1600R Mo-3 6y (F) TD 1.6 0.9 1.5 0.06 na nd [c.4465-34A>G,ins-33_-1]+[c.4465-34A>G,ins-33_-1], p.Q1488_1489insRPVCLVFM*9 Mo-4 32y (M) TD 1.3 na 2.1 0.03 0.4 b0.3 [c.4367delT]+[c.4367delT], p.M1456Sfs*45 Mo-5 6m (M) TD 2.5 0.57 1.5 0.13 na na [c.5449C>T]+[c.5449C>T], p.R1817* Mo-6 69y (F) FHD 3.7 2.7 1.5 0.3 0.97 0.4 [c.389G>A; c.5398A>C], p.R130K; p.N1800H+[wild type] Mo-7 37y (M) FHD 4.3 na 13.4 0.14 1.29 b0.3 [c.1195-27G>A,ins-25_-1], p.E398ins8V399Gfs*13+[wild type] Geߚ8 60y (F) FHD 5.6 3.6 3.5 0.72 1.16 1.0 [c.396_397insA], p.Q133Tfs*20+[wild type] Ge-9 54y (M) FHD 5.8 3.3 4.4 0.57 1.28 0.8 [c.3202C>T], p.R1068C+[wild type] Ge-10 52y (M) FHD 5.9 4.0 3.7 0.49 0.78 1.37 [c.5398A>C], p.N1800H+[wild type] TD = Tangier disease; FHD = familial HDL deficiency; y = years; m = months; M = males; F = females; na = not available, nd = not detectable.
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ABCA1 p.His1600Arg 22959828:134:88
status: NEW
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176 PolyPhen (PSIC score) SIFT (P score) p.R130K Possibly damaging (1.540) Predicted tolerated p.R1068C Probably damaging (3.143) Predicted not tolerated (0.00) p.D1099Y Probably damaging (3.047) Predicted not tolerated (0.00) p.H1600R Probably damaging (3.197) Predicted not tolerated (0.02) p.N1800H Possibly damaging (1.845) Predicted tolerated termination codon (p.R587Afs*43) and ii) a single nucleotide substitution (c.4799A>G) in exon 36, resulting in a novel missense mutation (p.H1600R) (Table 1).
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ABCA1 p.His1600Arg 22959828:176:225
status: NEW
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ABCA1 p.His1600Arg 22959828:176:486
status: NEW
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178 In silico analysis predicted that the p.H1600R mutation was probably damaging (Table 2).
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ABCA1 p.His1600Arg 22959828:178:40
status: NEW
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