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Table 2 Characteristics of 19 SNPs

From: SLC29A1 single nucleotide polymorphisms as independent prognostic predictors for survival of patients with acute myeloid leukemia: an in vitro study

Gene SNP HGVS Names ref SNP ID Global MAF Location Chromosome position
DCK SNP1 NM_000788.2:c.-201C > T rs2306744 0.060/130 exon 4:71859352
  SNP2 NM_000788.2:c.207 + 9846A > G rs12648166 0.458/998 intron 4:71873745
  SNP3 NM_000788.2:c.757-1205C > T rs4694362 0.467/1015 intron 4:71893864
  SNP4 NM_000788.2:c.165C > T rs4643786 0.227/494 exon 4:71895260
  SNP5 NM_000788.2:c.207 + 11338A > G rs7684954 0.197/430 intron 4:71875237
  SNP6 NM_000788.2:c.666-346 T > C rs936869 0.196/426 intron 4:71892036
  SNP7 NM_000788.2:c.92-1110 T > C rs3775289 0.193/419 intron 4:71862674
CDA SNP8 NM_000788.2:c.266 + 3264A > G rs1689924 0.482/1049 intron 1:20934796
  SNP9 NM_000788.2:c.267-4159C > T rs572529 0.350/761 intron 1:20936176
  SNP10 NM_000788.2:c.267-4087G > A rs477155 0.279/606 intron 1:20936248
  SNP11 NM_000788.2:c.154 + 1015A > G rs818202 0.480/1045 intron 1:20916791
  SNP12 NM_000788.2:c.155-7161G > A rs818199 0.386/840 intron 1:20924260
  SNP13 NM_000788.2:c.266 + 1809G > A rs10916827 0.345/752 intron 1:20933341
  SNP14 NM_000788.2:c.266 + 2751G > A rs527912 0.349/759 intron 1:20934283
  SNP15 NM_000788.2:c.208G > A rs60369023 0.002/4 exon 1:20931474
SLC29A1 SNP16 NM_001078174.1:c.30-549 T > C rs324148 0.228/496 intron 6:44196578
  SNP17 NM_001078174.1:c.1260-201A > G rs760370 0.344/750 intron 6:44200953
  SNP18 NM_001078174.1:c.29 + 913C > T rs9394992 0.290/631 intron 6:44195992
  SNP19 NM_001078174.1:c.-54-3077A > G rs693955 0.189/411 intron 6:44191920
  1. SNP, single-nucleotide polymorphism; rfID., reference SNP identification; HGVS Names, Human Genome Variation Societyname; MAF, minor allele frequency.