Table 2.

Functional analysis in previously characterized FH variants (n = 26)

TranscriptProteinExpressionGP hemolysis
HR50 (0.71-1.29)*
C3b binding
BD50 (0.33-1.67)*
DAA
(<12.5)*
FI cofactor activity (<2.5)*Classification
(this study)
Classification
(previously reported)
Reference
c.157C>T R53C 2.46 1.14 32.9 1.7 Pathogenic Pathogenic 31  
c.184G>A V62I 0.91 1.04 4.2 1.2 Benign Polymorphism 32  
c.232A>G R78G 3.36 1.68 36.6 19.7 Pathogenic Pathogenic 33  
c.524G>C R175P > 8 2.49 46.6 72.6 Pathogenic Pathogenic 34  
c.653G>A G218E 7.33 8.10 43.6 47.5 Pathogenic Nonexpressed 35  
c.1189G>A G397R W 1.12 — 20.5 2.3 Pathogenic Nonexpressed 36  
c.1198C>A Q400K 0.94 1.18 8.1 1.9 Benign Nonexpressed 22  
c.1204C>A H402Y 1.22 1.00 5.6 1.7 Benign Polymorphism — 
c.1231T>A S411T 1.00 0.98 7.9 1.8 Benign Benign 5  
c.1292G>A C431Y W 1.12 1.54 12.9 2.6 Pathogenic Nonexpressed 36  
c.1343G>A C448Y W 1.09 1.32 6.8 1.8 Pathogenic Nonexpressed 37  
c.1424A>C Y475S 0.93 1.02 6.4 1.7 Benign Nonexpressed 38  
c.2695T>G Y899D W 0.70 0.83 4.1 1.5 Pathogenic Nonexpressed 39  
c.2850G>T Q950H 1.14 1.52 9.7 1.6 Benign Polymorphism 40  
c.2867C>T T956M 1.19 0.81 7.7 1.9 Benign Polymorphism 31  
c.2918G>A C973Y W 1.11 0.80 6.5 1.9 Pathogenic Nonexpressed 41  
c.3148A>T N1050Y 1.07 1.77 7.8 1.6 Benign Polymorphism 42  
c.3231T>G C1077W W 1.20 1.11 11.1 3.9 Pathogenic Nonexpressed 43  
c.3355G>A D1119N 3.07 1.09 42.3 53.6 Pathogenic Pathogenic 31  
c.3356A>G D1119G 2.71 0.78 37.1 27.8 Pathogenic Pathogenic 44  
c.3425A>G Y1142C 5.03 8.78 60.3 73.7 Pathogenic Pathogenic 45  
c.3454T>A C1152S F     Pathogenic Nonexpressed 46  
c.3497C>T P1166L 2.71 6.93 48.3 32.9 Pathogenic Pathogenic 31  
c.3572C>T S1191L 1.13 1.08 25.6 18.8 Pathogenic Pathogenic 47  
c.3628C>T R1210C 1.51 1.20 8.8 2.1 Pathogenic Pathogenic 8  
c.3644G>A R1215Q 4.75 1.79 38.1 18.3 Pathogenic Pathogenic 16,48  
TranscriptProteinExpressionGP hemolysis
HR50 (0.71-1.29)*
C3b binding
BD50 (0.33-1.67)*
DAA
(<12.5)*
FI cofactor activity (<2.5)*Classification
(this study)
Classification
(previously reported)
Reference
c.157C>T R53C 2.46 1.14 32.9 1.7 Pathogenic Pathogenic 31  
c.184G>A V62I 0.91 1.04 4.2 1.2 Benign Polymorphism 32  
c.232A>G R78G 3.36 1.68 36.6 19.7 Pathogenic Pathogenic 33  
c.524G>C R175P > 8 2.49 46.6 72.6 Pathogenic Pathogenic 34  
c.653G>A G218E 7.33 8.10 43.6 47.5 Pathogenic Nonexpressed 35  
c.1189G>A G397R W 1.12 — 20.5 2.3 Pathogenic Nonexpressed 36  
c.1198C>A Q400K 0.94 1.18 8.1 1.9 Benign Nonexpressed 22  
c.1204C>A H402Y 1.22 1.00 5.6 1.7 Benign Polymorphism — 
c.1231T>A S411T 1.00 0.98 7.9 1.8 Benign Benign 5  
c.1292G>A C431Y W 1.12 1.54 12.9 2.6 Pathogenic Nonexpressed 36  
c.1343G>A C448Y W 1.09 1.32 6.8 1.8 Pathogenic Nonexpressed 37  
c.1424A>C Y475S 0.93 1.02 6.4 1.7 Benign Nonexpressed 38  
c.2695T>G Y899D W 0.70 0.83 4.1 1.5 Pathogenic Nonexpressed 39  
c.2850G>T Q950H 1.14 1.52 9.7 1.6 Benign Polymorphism 40  
c.2867C>T T956M 1.19 0.81 7.7 1.9 Benign Polymorphism 31  
c.2918G>A C973Y W 1.11 0.80 6.5 1.9 Pathogenic Nonexpressed 41  
c.3148A>T N1050Y 1.07 1.77 7.8 1.6 Benign Polymorphism 42  
c.3231T>G C1077W W 1.20 1.11 11.1 3.9 Pathogenic Nonexpressed 43  
c.3355G>A D1119N 3.07 1.09 42.3 53.6 Pathogenic Pathogenic 31  
c.3356A>G D1119G 2.71 0.78 37.1 27.8 Pathogenic Pathogenic 44  
c.3425A>G Y1142C 5.03 8.78 60.3 73.7 Pathogenic Pathogenic 45  
c.3454T>A C1152S F     Pathogenic Nonexpressed 46  
c.3497C>T P1166L 2.71 6.93 48.3 32.9 Pathogenic Pathogenic 31  
c.3572C>T S1191L 1.13 1.08 25.6 18.8 Pathogenic Pathogenic 47  
c.3628C>T R1210C 1.51 1.20 8.8 2.1 Pathogenic Pathogenic 8  
c.3644G>A R1215Q 4.75 1.79 38.1 18.3 Pathogenic Pathogenic 16,48  

Abnormal values are shown in bold type.

F, failed to express in vitro; GP, guinea pig; N, normal; W, weak (decreased) intensity of band corresponding to FH in nonreducing SDS-PAGE; –, not performed or not saturable binding (see “Individual variant datasheets” for details).

*

Normal ranges are in parenthesis. HR50 refers to the concentration fold of FH mutant needed to confer 50% protection from lysis compared with the wild-type FH protein in the guinea pig hemolysis assay; BD50 refers to the concentration fold of FH mutant needed to confer similar binding to C3b compared with the wild-type FH protein (see “Methods” for details).

FH variants that associate with quantitative deficiencies in patients but express normally in vitro and are functionally undistinguishable from the wild-type FH in vitro.

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