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. 2002 Mar 1;70(4):845–857. doi: 10.1086/339432

Table 2.

CARD15 Variants Observed in 453 Patients with CD, 159 Patients with UC, and 103 Healthy Control Subjects

No (%) of Variant Alleles in Patient Group
Location andNucleotideChange PeptideChange PolymorphicMarkera ProteinDomain CD (n=906) UC (n=318) Control (n=206)
Exon 2:
 5′ UTR-37 T→G Unknown 2 1 0
 5′ UTR-33 G→T Unknown 380 (42) 79 (25) 68 (33)
 5′ UTR-15 T→A Unknown 1 0 1
 315 G→A A105A CARD1 1 0 0
 357 G→T L119L CARD1 1 0 0
413 G→A R138Q CARD2 1 0 0
418 G→A A140T CARD2 1 1 0
469 T→C W157R CARD2 1 0 0
 534 C→G S178S CARD2 280 (31) 135 (42) 79 (38)
Exon 3:
566 C→T T189M CARD2 0 1 2
 633 C→T A211A CARD2 0 1 0
Exon 4:
703 C→T R235C 1 0 0
743 T→G L248R 1 0 0
802 C→T P268S SNP5 375 (41) 77 (24) 57 (28)
866 A→G N289S NBD 6 0 3
871 G→A D291N NBD 1 0 0
 881 C→G T294S NBD 1 0 0
 902 C→T A301V NBD (P Loop) 1 0 0
931 C→T R311W NBD 2 1 0
 1042 C→G L348V NBD 1 0 0
 1055 A→G H352R NBD 2 0 0
1117 C→T R373C NBD 1 0 0
1241 A→G N414S NBD 1 0 0
 1281 G→A P427P NBD 2 0 0
1292 C→T S431L NBD 1 0 0
 1295 C→T A432V NBD 1 0 0
1321 G→A E441K NBD 1 0 0
 1366 C→T L456L NBD 0 0 1
 1377 C→T R459R SNP6 NBD 379 (42) 76 (24) 59 (29)
 1509 G→A E503E NBD 0 1 0
 1581 C→G P527P NBD 0 1 0
1671 delCCTGGG 558delLG NBD 1 0 0
 1761 T→G R587R SNP7 301 (33) 142 (45) 83 (40)
 1788 G→A T596T 1 0 0
 1833 C→T A611A 3 6 5
1834 G→A A612T 1 0 0
 1835 C→T A612V 2 0 0
2050 C→T R684W 1 0 0
2104 C→T R702W SNP8 98 (11) 10 (3) 9 (4)
2107 C→T R703C 11 1 0
2137 C→T R713C 1 0 0
 2174 C→G A725G 3 0 0
 2220 C→T I740I 1 0 0
 2264 C→T A755V LRR1 11 1 0
 2273 C→T A758V LRR1 1 0 0
2332 G→A E778K LRR2 3 0 0
2377 G→A V793M LRR2 4 0 0
IVS4:
 IVS4+10 A→C Unknown 14 0 0
Exon 5:
2527 G→A E843K LRR4 1 0 0
Exon 6:
2558 A→G N853S LRR5 2 0 0
2587 A→G M863V LRR5 4 0 0
 2619 C→T F873F LRR5 1 0 0
(continued)