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. Author manuscript; available in PMC: 2009 Mar 2.

Published in final edited form as: Hum Mutat. 2009 Mar;30(3):E467–E480. doi: 10.1002/humu.20932

Table 2.

SNPs and neutral variants observed

Gene	Allele^a		Frequency^b
	c.2088A>G	p.I696M	0.03
PEX1	c.2331C>A	p.G777G	0.84
	c.3762T>C	p.A1254A	0.01^c

	c.210G>A	p.G70G	0.01^c
	c.235G>C	p.A79P	0.02
	c.399G>T	p.V133V	0.37
	c.813G>T	p.A271A	0.01^c
	c.1802G>A	p.R601Q	0.03
PEX6	c.2364G>A	p.V788V	0.04
	c.2426C>T	p.A809V	0.03
	c.2644G>A	p.V882I	0.03
	c.2770G>T	p.A924S	0.01^c
	c.2814G>A	p.E938E	0.43
	c.2816C>A	p.P939Q	0.35

PEX10	c.820A>G	p.T274A	0.03

PEX12	c.733T>A	p.L245I	0.01^c
PEX12	c.867C>T	p.D289D	0.01^c

PEX26	c.457C>G	p.L153V	0.03

^a

Newly discovered silent variants in red

^b

Based on the analysis of 116 chromosomes

^c

Allele found only once in cohort