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Table 2 Results of molecular analysis for DNA from 45 PH-1 Syrian patients

From: Molecular analysis of the AGXT gene in Syrian patients suspected with primary hyperoxaluria type 1

Mutation Exon Maj/min Number of alleles Allele frequency (%)
c.33_34insC 1 Maj 30 33.3
c.584 T > G 5 Min 11 12.2
c.1007 T > A 10 Min 10 11.1
c.322 T > C 2 Min 6 6.7
c.971-972delTG 10 Maj 6 6.7
c.198C > A 2 Maj 5 5.6
c.508G > A 4 Min 4 4.4
c.305 T > A 2 Min 2 2.2
c.602A > T 6 Min 2 2.2
c.866G > A 9 Maj 2 2.2
c.603C > A 6 Maj 2 2.2
c.359-1_382del 3 Maj 2 2.2
c.731 T > C 7 Min 1 1.1
c.140G > A 1 Min 1 1.1
c.941C > T 9 Min 1 1.1
c.1078C > T 11 Maj 1 1.1
c.997A > T 10 Maj 1 1.1