Single Nucleotide Polymorphism (SNP) and indel
|
Location |
Variation |
dbSNP ID |
Strand |
CDS/UTR |
Translation |
73
..
73
|
C/G |
rs142556794
|
+ |
CDS |
Nonsynonymous[Ala24Gly] |
82
..
82
|
C/T |
rs2669142
|
- |
CDS |
Nonsynonymous[Ala27Val] |
225
..
225
|
C/T |
rs201255154
|
+ |
CDS |
Nonsynonymous[Arg75Cys] |
241
..
241
|
C/T |
rs200385091
|
+ |
CDS |
Nonsynonymous[Thr80Met] |
278
..
278
|
A/G |
rs2797492
|
+ |
CDS |
Synonymous[Leu92Leu] |
325
..
325
|
C/G |
rs201339737
|
+ |
CDS |
Nonsynonymous[Thr108Arg] |
373
..
373
|
T/C |
rs188774714
|
+ |
CDS |
Nonsynonymous[Val124Ala] |
384
..
384
|
T/G |
rs192382862
|
+ |
CDS |
Nonsynonymous[Phe128Val] |
391
..
391
|
C/T |
rs11593253
|
+ |
CDS |
Nonsynonymous[Thr130Ile] |
400
..
400
|
G/A |
rs183849963
|
+ |
CDS |
Nonsynonymous[Cys133Tyr] |
516
..
516
|
T/A |
rs201296998
|
+ |
CDS |
Nonsynonymous[Tyr172Asn] |
552
..
552
|
G/A |
rs186674940
|
+ |
CDS |
Nonsynonymous[Gly184Ser] |
577
..
577
|
A/T |
rs150562707
|
+ |
CDS |
Nonsynonymous[Asp192Val] |
635
..
635
|
A/C |
rs200042693
|
+ |
CDS |
Synonymous[Thr211Thr] |
638
..
638
|
T/C |
rs11255020
|
+ |
CDS |
Synonymous[Asp212Asp] |
712
..
712
|
T/C |
rs200680802
|
+ |
CDS |
Nonsynonymous[Met237Thr] |
714
..
714
|
G/A |
rs200299323
|
+ |
CDS |
Nonsynonymous[Glu238Lys] |
783
..
783
|
G/A |
rs199718858
|
+ |
CDS |
Nonsynonymous[Val261Ile] |
857
..
857
|
C/T |
rs199607512
|
+ |
CDS |
Synonymous[Thr285Thr] |
860
..
860
|
G/C |
rs200720899
|
+ |
CDS |
Nonsynonymous[Met286Ile] |
873
..
873
|
G/A |
rs139283778
|
+ |
CDS |
Nonsynonymous[Gly291Ser] |
960
..
960
|
C/G |
rs191866446
|
+ |
CDS |
Nonsynonymous[Gln320Glu] |
961
..
961
|
A/G |
rs200658639
|
+ |
CDS |
Nonsynonymous[Gln320Arg] |
988
..
988
|
G/A |
rs150013388
|
+ |
CDS |
Nonsynonymous[Arg329His] |
1003
..
1003
|
T/A |
rs184717923
|
+ |
CDS |
Nonsynonymous[Leu334Gln] |
1026
..
1026
|
G/T |
rs76593109
|
+ |
CDS |
Nonsynonymous[Asp342Tyr] |
1054
..
1054
|
A/G |
rs61729836
|
+ |
CDS |
Nonsynonymous[Asn351Ser] |
1157
..
1157
|
C/T |
rs201588583
|
+ |
CDS |
Synonymous[Ser385Ser] |
1160
..
1160
|
C/T |
rs61729837
|
+ |
CDS |
Synonymous[Pro386Pro] |
1215
..
1215
|
G/C |
rs201298628
|
+ |
CDS |
Nonsynonymous[Gly405Arg] |
1240
..
1240
|
G/T |
rs45596231
|
+ |
CDS |
Nonsynonymous[Ser413Ile] |
1246
..
1246
|
C/T |
rs78976120
|
+ |
CDS |
Nonsynonymous[Ser415Phe] |
1290
..
1290
|
T/A |
rs181734097
|
+ |
CDS |
Nonsynonymous[Ser430Thr] |
1304
..
1304
|
C/T |
rs61729838
|
+ |
CDS |
Synonymous[His434His] |
1314
..
1314
|
T/C |
rs185121400
|
+ |
CDS |
Nonsynonymous[Phe438Leu] |
1384
..
1384
|
A/G |
rs76566496
|
+ |
CDS |
Nonsynonymous[Asn461Ser] |
1467
..
1467
|
G/A |
rs201253142
|
+ |
CDS |
Nonsynonymous[Glu489Lys] |
1481
..
1481
|
A/G |
rs144652739
|
+ |
CDS |
Synonymous[Gln493Gln] |
1496
..
1496
|
T/C |
rs200805732
|
+ |
CDS |
Synonymous[Pro498Pro] |
1557
..
1557
|
G/A |
rs147954390
|
+ |
CDS |
Nonsynonymous[Val519Ile] |
1638
..
1638
|
T/G |
rs189397135
|
+ |
CDS |
Nonsynonymous[Phe546Val] |
1641
..
1641
|
G/A |
rs200227576
|
+ |
CDS |
Nonsynonymous[Val547Ile] |
1909
..
1909
|
A/G |
rs2275774
|
+ |
CDS |
Nonsynonymous[Lys636Arg] |
2030
..
2030
|
A/T |
rs202125233
|
+ |
CDS |
Nonsynonymous[Glu676Asp] |
2060
..
2060
|
G/C |
rs187381778
|
+ |
CDS |
Nonsynonymous[Lys686Asn] |
2150
..
2150
|
A/G |
rs145466559
|
+ |
CDS |
Synonymous[Ala716Ala] |
2154
..
2154
|
A/G |
rs41290259
|
+ |
CDS |
Nonsynonymous[Ile718Val] |
2166
..
2166
|
T/C |
rs191790060
|
+ |
CDS |
Synonymous[Leu722Leu] |
2214
..
2214
|
C/T |
rs148894359
|
+ |
CDS |
Synonymous[Leu738Leu] |
Microsatellite (Short Tandem Repeat, STR) |
No data available |
Microsatellite: Human-Gene diversity Of Life-style related Diseases (H-GOLD) |
No data available |
|
Repeat
|
No data available |
|