Single Nucleotide Polymorphism (SNP) and indel
|
Location |
Variation |
dbSNP ID |
Strand |
CDS/UTR |
Translation |
2
..
2
|
G/C |
rs7501500
|
- |
5'UTR |
|
122
..
122
|
G/T |
rs11658876
|
- |
CDS |
Nonsynonymous[Ala17Ser] |
166
..
166
|
T/G |
rs150024312
|
- |
CDS |
Nonsynonymous[Asp31Glu] |
201
..
201
|
G/T |
rs2233665
|
+ |
CDS |
Nonsynonymous[Arg43Leu] |
202
..
202
|
T/G |
rs147481037
|
- |
CDS |
Synonymous[Arg43Arg] |
225
..
225
|
G/T |
rs201359263
|
- |
CDS |
Nonsynonymous[Gly51Val] |
336
..
336
|
T/C |
rs121918373
|
+ |
CDS |
Nonsynonymous[Val88Ala] |
370
..
370
|
C/T |
rs144654469
|
- |
CDS |
Synonymous[Val99Val] |
387
..
387
|
G/A |
rs121918372
|
+ |
CDS |
Nonsynonymous[Arg105His] |
396
..
396
|
C/G |
rs199792568
|
- |
CDS |
Nonsynonymous[Thr108Ser] |
405
..
405
|
G/A |
rs1049515
|
+ |
CDS |
Nonsynonymous[Gly111Glu] |
412
..
412
|
C/T |
rs1049517
|
+ |
CDS |
Synonymous[Asp113Asp] |
499
..
499
|
G/A |
rs1049525
|
+ |
CDS |
Synonymous[Gln142Gln] |
517
..
517
|
G/T |
rs140693016
|
- |
CDS |
Nonsynonymous[Arg148Ser] |
547
..
547
|
C/T |
rs201875820
|
- |
CDS |
Synonymous[Ala158Ala] |
597
..
597
|
T/G |
rs150607417
|
- |
CDS |
Nonsynonymous[Phe175Cys] |
598
..
598
|
C/T |
rs191710304
|
- |
CDS |
Synonymous[Phe175Phe] |
613
..
613
|
A/G |
rs141363200
|
- |
CDS |
Synonymous[Thr180Thr] |
619
..
619
|
G/A |
rs148262252
|
- |
CDS |
Synonymous[Ala182Ala] |
721
..
721
|
C/T |
rs144040543
|
- |
CDS |
Synonymous[Gly216Gly] |
751
..
751
|
C/T |
rs149508639
|
- |
CDS |
Synonymous[Asn226Asn] |
781
..
781
|
C/T |
rs142883213
|
- |
CDS |
Synonymous[Ile236Ile] |
782
..
782
|
G/A |
rs137958073
|
- |
CDS |
Nonsynonymous[Glu237Lys] |
826
..
826
|
C/T |
rs2233670
|
+ |
CDS |
Synonymous[Leu251Leu] |
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 |
|