Single Nucleotide Polymorphism (SNP) and indel
|
Location |
Variation |
dbSNP ID |
Strand |
CDS/UTR |
Translation |
107
..
107
|
G/T |
rs11658876
|
- |
CDS |
Nonsynonymous[Ala17Ser] |
151
..
151
|
T/G |
rs150024312
|
- |
CDS |
Nonsynonymous[Asp31Glu] |
186
..
186
|
G/T |
rs2233665
|
+ |
CDS |
Nonsynonymous[Arg43Leu] |
187
..
187
|
T/G |
rs147481037
|
- |
CDS |
Synonymous[Arg43Arg] |
210
..
210
|
G/T |
rs201359263
|
- |
CDS |
Nonsynonymous[Gly51Val] |
321
..
321
|
T/C |
rs121918373
|
+ |
CDS |
Nonsynonymous[Val88Ala] |
355
..
355
|
C/T |
rs144654469
|
- |
CDS |
Synonymous[Val99Val] |
372
..
372
|
G/A |
rs121918372
|
+ |
CDS |
Nonsynonymous[Arg105His] |
381
..
381
|
C/G |
rs199792568
|
- |
CDS |
Nonsynonymous[Thr108Ser] |
390
..
390
|
G/A |
rs1049515
|
+ |
CDS |
Nonsynonymous[Gly111Glu] |
397
..
397
|
C/T |
rs1049517
|
+ |
CDS |
Synonymous[Asp113Asp] |
484
..
484
|
G/A |
rs1049525
|
+ |
CDS |
Synonymous[Gln142Gln] |
502
..
502
|
G/T |
rs140693016
|
- |
CDS |
Nonsynonymous[Arg148Ser] |
532
..
532
|
C/T |
rs201875820
|
- |
CDS |
Synonymous[Ala158Ala] |
582
..
582
|
T/G |
rs150607417
|
- |
CDS |
Nonsynonymous[Phe175Cys] |
583
..
583
|
C/T |
rs191710304
|
- |
CDS |
Synonymous[Phe175Phe] |
598
..
598
|
A/G |
rs141363200
|
- |
CDS |
Synonymous[Thr180Thr] |
604
..
604
|
G/A |
rs148262252
|
- |
CDS |
Synonymous[Ala182Ala] |
706
..
706
|
C/T |
rs144040543
|
- |
CDS |
Synonymous[Gly216Gly] |
736
..
736
|
C/T |
rs149508639
|
- |
CDS |
Synonymous[Asn226Asn] |
766
..
766
|
C/T |
rs142883213
|
- |
CDS |
Synonymous[Ile236Ile] |
767
..
767
|
G/A |
rs137958073
|
- |
CDS |
Nonsynonymous[Glu237Lys] |
811
..
811
|
C/T |
rs2233670
|
+ |
CDS |
Synonymous[Leu251Leu] |
887
..
887
|
C/G |
rs2233671
|
+ |
3'UTR |
|
902
..
902
|
C/T |
rs200124498
|
- |
3'UTR |
|
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 |
|