Identification of ITGA2B and ITGB3 Single-Nucleotide Polymorphisms and Their Influences on the Platelet Function
Table 3
Summary of ITGB3 variations detected in this study.
Sequence number obtained in this study
dbSNP
Location
NC_000017.11
NM_000212.2
Nucleotide change
NP_000410.2 amino acid change
MA(F)
H-W
ITGB3-01
rs147363351
5′-UTR
47253042
-820
agcttccaga G/A gttttaagtc
A(0.012)
0.913
ITGB3-02
rs3809862
5′-UTR
47253062
-800
ctggggaaga C/T ccagggactc
T(0.424)
0.822
ITGB3-03
rs7208170
5′-UTR
47253393
-469
aaggcattca G/A cagatgtttg
A(0.419)
0.680
ITGB3-04
New
5′-UTR
47253360
-502
tagtgaataa T/A aaaggactga
A(0.023)
0.913
ITGB3-05
rs7208055
5′-UTR
47253461
-401
gtgaatgtgt C/A ccaagaatcc
A(0.221)
0.273
ITGB3-06
rs55827077
5′-UTR
47253717
-145
tagagaagcc G/C gaggggagga
C(0.448)
0.494
ITGB3-07
rs567581451
5′-UTR
47253771
-91
acccaccgcg -/TCCCC tcccctcccc
insTCCCC(0.058)
0.567
ITGB3-08
rs117052258
5′-UTR
47253855
-7
cgcgggaggc G/C gacgagatgc
C(0.227)
0.771
ITGB3-09
New
Exon1
47253882
21
ggccgcggcc C/G cggccgctct
Pro7=
G(0.407)
0.567
ITGB3-10
rs11871251
Intron1
47254061
79+121
ctgggaatgc G/A cgtgtcctgg
A(0.453)
0.771
ITGB3-11
New
Intron1
47254082
79+152
tggcgcggt C/G ggagccggga
G(0.012)
0.913
ITGB3-12
rs112188890
Intron1
47254101
79+161
gagctgggga C/T cttcctggcc
T(0.116)
0.864
ITGB3-13
rs117414137
Intron1
47254192
79+252
aggctgagcg C/G cttcccggcc
G(0.116)
0.864
ITGB3-14
rs11871447
Intron1
47254252
79+312
ccgcgctcac C/G cggggctgcg
G(0.448)
0.918
ITGB3-15
New
Intron1
47254331
79+391
tggggcttcc G/A ggggttgttc
A(0.006)
0.957
ITGB3-16
rs1009312
Intron1
47254774
79+834
ggcacagccc G/A gggttgctgc
G(0.471)
0.000
ITGB3-17
rs2015049
Intron1
47254865
79+925
ggccgcctct G/A cctcagagga
A(0.529)
0.000
ITGB3-18
rs56197296
Intron5
47287025_47287029
778-45_778-41
catggctgaa TTTGT/- tttgtctcct
delTTTGT(0.169)
0.049
ITGB3-19
rs5919
Exon6
47287174
882
ttgtccagcc T/C aatgacgggc
Pro294=
C(0.262)
0.022
ITGB3-20
rs41504748
Intron7
47290145
1036-40
accaccagct T/C cctttggtaa
C(0.070)
0.334
ITGB3-21
rs15908
Exon9
47290971
1143
cttccagctc A/G/T actttagaac
Val381=
C(0.599)
0.006
ITGB3-22
New
Exon10
47292177
1299
gaggctgtcc C/T caggagaagg
Pro433=
T(0.006)
0.957
ITGB3-23
rs4642
Exon10
47292411
1533A>G
cagcaggacga A/G tgcagccccc
Glu511=
G(0.331)
0.214
ITGB3-24
rs13306487
Exon10
47292422
1544
tgcagccccc A/C/G ggagggtcag
Arg515Gln
A(0.012)
0.913
ITGB3-25
rs4634
Exon10
47292423
1545
gcagcccccg G/A gagggtcagc
Arg515=
A(0.331)
0.214
ITGB3-26
New
Exon10
47292528
1659
gcgagtgtga C/Tgacttctcct
Asp550=
T(0.006)
0.957
ITGB3-27
rs149823724
Exon11
47299519
1902
cagatgcctg C/T acctttaaga
Cys634=
T(0.006)
0.957
ITGB3-28
rs11870252
Intron11
47300459
1914-19
ccttaatcac T/C gtgtcctctc
C(0.035)
0.869
ITGB3-29
rs70940817
Exon12
47300524
1960
cctacatgac G/A aaaatacctg
Glu654Lys
A(0.076)
0.432
dbSNP, single nucleotide polymorphism database; H-W , Hardy–Weinberg equilibrium value; MA(F), minor allele (frequency). SNPs which related with ADP induced platelets aggregation, GPIIb/IIIa content, bleeding time, or coagulation indexes in this study.