Single Nucleotide Polymorphism (SNP) and indel
|
Location |
Variation |
dbSNP ID |
Strand |
CDS/UTR |
Translation |
96
..
96
|
G/T |
rs11658876
|
- |
CDS |
Nonsynonymous[Ala17Ser] |
140
..
140
|
T/G |
rs150024312
|
- |
CDS |
Nonsynonymous[Asp31Glu] |
175
..
175
|
G/T |
rs2233665
|
+ |
CDS |
Nonsynonymous[Arg43Leu] |
176
..
176
|
T/G |
rs147481037
|
- |
CDS |
Synonymous[Arg43Arg] |
199
..
199
|
G/T |
rs201359263
|
- |
CDS |
Nonsynonymous[Gly51Val] |
310
..
310
|
T/C |
rs121918373
|
+ |
CDS |
Nonsynonymous[Val88Ala] |
344
..
344
|
C/T |
rs144654469
|
- |
CDS |
Synonymous[Val99Val] |
361
..
361
|
G/A |
rs121918372
|
+ |
CDS |
Nonsynonymous[Arg105His] |
370
..
370
|
C/G |
rs199792568
|
- |
CDS |
Nonsynonymous[Thr108Ser] |
379
..
379
|
G/A |
rs1049515
|
+ |
CDS |
Nonsynonymous[Gly111Glu] |
386
..
386
|
C/T |
rs1049517
|
+ |
CDS |
Synonymous[Asp113Asp] |
473
..
473
|
G/A |
rs1049525
|
+ |
CDS |
Synonymous[Gln142Gln] |
491
..
491
|
G/T |
rs140693016
|
- |
CDS |
Nonsynonymous[Arg148Ser] |
521
..
521
|
C/T |
rs201875820
|
- |
CDS |
Synonymous[Ala158Ala] |
571
..
571
|
T/G |
rs150607417
|
- |
CDS |
Nonsynonymous[Phe175Cys] |
572
..
572
|
C/T |
rs191710304
|
- |
CDS |
Synonymous[Phe175Phe] |
587
..
587
|
A/G |
rs141363200
|
- |
CDS |
Synonymous[Thr180Thr] |
593
..
593
|
G/A |
rs148262252
|
- |
CDS |
Synonymous[Ala182Ala] |
695
..
695
|
C/T |
rs144040543
|
- |
CDS |
Synonymous[Gly216Gly] |
725
..
725
|
C/T |
rs149508639
|
- |
CDS |
Synonymous[Asn226Asn] |
755
..
755
|
C/T |
rs142883213
|
- |
CDS |
Synonymous[Ile236Ile] |
756
..
756
|
G/A |
rs137958073
|
- |
CDS |
Nonsynonymous[Glu237Lys] |
800
..
800
|
C/T |
rs2233670
|
+ |
CDS |
Synonymous[Leu251Leu] |
876
..
876
|
C/G |
rs2233671
|
+ |
3'UTR |
|
891
..
891
|
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 |
|