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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.