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. 2007 Apr 4;13:534–544.

Table 1. Genotyping of MYOC microsatellites and single nucleotide polymorphisms.

Marker
Marker type/assay method
Primer/probe/assay ID
5'-3' Sequence/allele (probe signal)
NGA17
MS/Fragment analysis
Myocpm-F
FLU-GGCTGTTATTTTTCTCTGT


Myocpm-R
TGCCAGCAAGATTCTTAGAA
NGA19
MS/Fragment analysis
Myoc3pm-F
FLU-GTTGGGAGATGTGATTGCAG


Myoc3pm-R
AGATGGAGGTGGGAAAGTGT
rs7523603
SNP/TaqMan Assay-by-Design
Myocil-F
CGGACCCAGAGCGAAGTT


Myocil-R
AGGGCTGTGGAAAGGTTATGG


A allele-specific probe
VIC-CTGTGAGGTCAC[A]GAAG-MGB


G allele-specific probe
FAM-TGTGAGGTCAC[G]GAAG-MGB
rs2075537
SNP/TaqMan Assay-on-Demand
C_27532255_10
T (VIC) and G (FAM)
rs235920
SNP/TaqMan Assay-on-Demand
C_558534_10
T (VIC) and C (FAM)
rs2421853
SNP/TaqMan Assay-on-Demand
C_11335131_10
A (VIC) and G (FAM)
rs235858 SNP/TaqMan Assay-on-Demand C_2964922_10 A (VIC) and G (FAM)

Forward primers that amplified microsatellites (MS) were labeled with fluorescein (FLU). Four single nucleotide polymorphisms (SNPs) were genotyped by assay-on-demand TaqMan. Only assay identifications and allele-specific probe signals were provided by the manufacturer. All allele-specific probes were labeled with a reporter dye (either VIC or FAM) at the 5' end, and a quencher and a minor groove-binder (MGB) at the 3' end. Bases in square brackets indicate the positions of the bases defining the alleles of the SNPs that were to be detected by the probes.