Table 3.
NucleotideSubstitution | No. ofCases | Amino Acid Substitution | Domain |
Exon 2: | |||
124A→G | 2 | Thr42Ala | N-SH2 |
Exon 3: | |||
179G→C | 2 | Gly60Ala | N-SH2 |
181G→A | 1 | Asp61Asn | N-SH2 |
182A→G | 2 | Asp61Gly | N-SH2 |
184T→G | 2 | Tyr62Asp | N-SH2 |
188A→G | 4 | Tyr63Cys | N-SH2 |
215C→G | 1 | Ala72Gly | N-SH2 |
218C→T | 1 | Thr73Ile | N-SH2 |
228G→C | 1 | Glu76Asp | N-SH2 |
236A→G | 5 | Gln79Arg | N-SH2 |
317A→C | 3 | Asp106Ala | N-SH2/C-SH2 linker |
Exon 4: | |||
417G→C | 1 | Glu139Asp | C-SH2 |
417G→T | 1 | Glu139Asp | C-SH2 |
Exon 7: | |||
836A→G | 1 | Tyr279Cys | PTP |
844A→G | 1 | Ile282Val | PTP |
853T→C | 1 | Phe285Leu | PTP |
Exon 8: | |||
854T→C | 1 | Phe285Ser | PTP |
922A→G | 17 | Asn308Asp | PTP |
923A→Ga | 2 | Asn308Ser | PTP |
925A→G | 1 | Ile309Val | PTP |
Exon 13: | |||
1502G→A | 1 | Arg501Lys | PTP |
1510A→G | 3 | Met504Val | PTP |
Affected members of one family segregating the 923A→G change (Asn308Ser) exhibited the Noonan-like/multiple giant-cell lesion condition.