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. 2014 Jan 23;18(3):333–342. doi: 10.1007/s40291-014-0083-6

Table 1.

Primers and probes for genotyping

Polymorphism Position WT>variant Primer or Probe
UGT1A1*6 211 G>A C 559715 20
UGT1A1*27 686 C>A C 2307598 20
UGT1A1*28 TATA box TA6>TA7

F-FAM

R

5′-gtgacacagtcaaacattaacttgt-3′

5′-gcctttgctcctgccagaggtt-3′

UGT1A1*60 −3279 T>G C 1432134 10
UGT1A1*93 −3156 G>A

F

R

FAM

VIC

5′-acttaacattgcagcacagg-3′

5′-atgggcaaaagccttgaact-3′

5′-cctgtccaagctca-3′

5’-cacctgtctaagctca-3’

UGT1A7*2 (N129K) UGT1A7*3 (W208R)

387

622

T>G

T>C

F

R

5′-tacactctggaggatcagga-3′

5′-tattgggcatcacgggtttg-3′

UGT1A7*12 −57 T>G C 287265 10
UGT1A9* 22 −188 T9>T10 F 5′-acttaacattgcagcacagg-3′
R 5′-atgggcaaaagccttgaact-3′

Nucleotide positions are relative to the transcription start site

Transposition of T to G at position 387 (or N129K) is termed UGT1A7*2. Transposition of T to C at position 622 is termed W208R, and co-occurrence of N129K and W208R is termed UGT1A7*3

TA6 6 TA repeats, TA7 7 TA repeats, F-FAM forward primer-labeled reporter 1 probe, F forward primer, R reverse primer, FAM reporter 1 probe, VIC reporter 2 probe, WT wild type