Table 1 Summary of FLNB missense mutations.
Family ID | DNA mutation | Exon | Predicted amino | Domain | Reference |
---|---|---|---|---|---|
acid change | |||||
319 | 482T→G | 2 | F161C | CHD2 | 15 |
LR9 | 479A→C | 2 | N160T | CHD2 | This study |
LR1 | 679G→A | 4 | E227K** | CHD2 | This study; 15 |
CF16 | 4604G→A | 27 | S1535N | 14 | This study |
LR7 | 4640C→A | 27 | A1547D | 14 | This study |
318 | 4711_4713del AAT | 28 | 1571delN | 14 | 15 |
334 | 4756CG→A | 28* | G1586R | 14 | 15 |
LR6 | 4930G →T | 29 | G1644W | 15 | This study |
LR11 | 5071G →T | 29 | G1691S** | 15 | This study; 15 |
Mutations and their predicted amino acid substitutions are shown in exon order. *Exons are numbered as depicted in the Ensembl genome browser (www.ensembl.org) and differ slightly from numbering reported by Krakow et al.15
**Previously reported.17