Table 2 Polymorphisms in the H1 haplotype
From: Role of MAPT mutations and haplotype in frontotemporal lobar degeneration in Northern Finland
Exon | Position Relative to Exon | Codon | Nucleotide Change | Allele Frequency in Patients with FTLD |
|---|---|---|---|---|
Exon 1 | T39T | ACG > ACA | 3 | |
Exon 2 | T52A | ACT > GCT | 1 | |
Exon 9 | P270P | CCG > CCA | 1 | |
Exon 10 | -47 | C > A | 2 | |
Exon 11 | +90 | G > A | 16 | |
Exon 11 | +104 | A > G | 1 | |
Exon 13 | +67 | del AAT | 10 |