Table 3 Clinically relevant mutations and their corresponding oligonucleotide sequences.

From: Cost-effective and robust genotyping using double-mismatch allele-specific quantitative PCR

  

allele

allele-specific primers

common primer

rs113488022

BRAF (V600E)

A/T

AATAGGTGATTTTGGTCTAGCTACAG[A/T]

GTAACTCAGCAGCATCTCAGGG

rs113993960

CF (deltaF508)

C/T

GCCTGGCACCATTAAAGAAAATATCAT[C/T]

GGCATGCTTTGATGACGCTTC

rs6025

Leiden mutation (FCTRV)

C/T

ACTTCAAGGACAAAATACCTGTATTCCT[C/T]

TCGCCTCTGGGCTAATAGGAC

rs77375493

JAK2 (V617F)

A/C

AGTTTTACTTACTCTCGTCTCCACAGA[A/C]

AGCAGCAAGTATGATGAGCAAGC

COSM28057

ALK (F1174L_A > G)

C/T

CCTCTCTGCTCTGCAGCAAA[C/T]

GGGTCTCTCGGAGGAAGGAC

COSM28059

ALK (F1174C)

A/G

CCTCTCTGCTCTGCAGCAAAT[G/T]

GGGTCTCTCGGAGGAAGGAC

COSM28055

ALK (F1174L_G > T)

A/C

CTCTCTGCTCTGCAGCAAATT[A/C]

GGGTCTCTCGGAGGAAGGAC

COSM28056

ALK (R1275Q)

C/T

CAGTCTTTACTCACCTGTAGATGTCT[C/T]

GCCAGAAACTGCCTCTTGACC

rs17851045

KRAS (codon 61)

A/T

CCCTCATTGCACTGTACTCCTC[A/T]

TTGTCCGTCATCTTTGGAGCAG

COSM12429

EGFR (L858R)

G/T

TGTCAAGATCACAGATTTTGGGC[G/T]

CTAGTGGGAAGGCAGCCTGG

COSM6252

EGFR (G719S)

A/G

ACTGAATTCAAAAAGATCAAAGTGCTG[A/G]

AGACCATGAGAGGCCCTGC

COSM6253

EGFR (G719C_G > T)

G/T

ACTGAATTCAAAAAGATCAAAGTGCTG[G/T]

AGACCATGAGAGGCCCTGC

COSM18441

EGFR (G719C_GG > TT)

A/C

GAACGCACCGGAGCC[A/C]

TGGAGCCTCTTACACCCAGTG

COSM6239

EGFR (G719A)

C/G

TGAATTCAAAAAGATCAAAGTGCTGG[C/G]

GCTCCCCACCAGACCATGAG

COSM6240

EGFR (T790M)

C/T

CCACCGTGCAGCTCATCA[C/T]

AGCAGGTACTGGGAGCCAAT

  1. Mismatches and allele-specific nucleotides are marked bold and underlined.