Single Nucleotide Polymorphism (SNP) and indel
|
Location |
Variation |
dbSNP ID |
Strand |
CDS/UTR |
Translation |
163
..
163
|
G/C |
rs12841023
|
+ |
CDS |
Nonsynonymous[Gln17His] |
177
..
177
|
C/G |
rs139200954
|
+ |
CDS |
Nonsynonymous[Ala22Gly] |
261
..
261
|
C/T |
rs201489369
|
+ |
CDS |
Nonsynonymous[Pro50Leu] |
270
..
270
|
C/A |
rs142614402
|
+ |
CDS |
Nonsynonymous[Ala53Asp] |
275
..
275
|
G/A |
rs150572851
|
+ |
CDS |
Nonsynonymous[Ala55Thr] |
286
..
286
|
G/A |
rs139614533
|
+ |
CDS |
Synonymous[Ala58Ala] |
308
..
308
|
G/A |
rs149753411
|
+ |
CDS |
Nonsynonymous[Ala66Thr] |
313
..
313
|
G/A |
rs61753429
|
+ |
CDS |
Synonymous[Glu67Glu] |
322
..
322
|
A/G |
rs141512330
|
+ |
CDS |
Synonymous[Arg70Arg] |
379
..
379
|
G/A |
rs201336096
|
+ |
CDS |
Synonymous[Gly89Gly] |
407
..
407
|
G/A |
rs184815507
|
+ |
CDS |
Nonsynonymous[Gly99Ser] |
414
..
414
|
C/T |
rs200599207
|
+ |
CDS |
Nonsynonymous[Thr101Met] |
415
..
415
|
G/A |
rs145355350
|
+ |
CDS |
Synonymous[Thr101Thr] |
451
..
451
|
C/T |
rs147681544
|
+ |
CDS |
Synonymous[Arg113Arg] |
464
..
464
|
C/T |
rs149177751
|
+ |
CDS |
Nonsynonymous[Pro118Ser] |
473
..
473
|
G/A |
rs200509606
|
+ |
CDS |
Nonsynonymous[Val121Met] |
591
..
591
|
A/G |
rs59609788
|
+ |
CDS |
Nonsynonymous[Asn160Ser] |
592
..
592
|
T/C |
rs143332634
|
+ |
CDS |
Synonymous[Asn160Asn] |
613
..
613
|
C/T |
rs148357840
|
+ |
CDS |
Synonymous[Asp167Asp] |
683
..
683
|
C/T |
rs140561920
|
+ |
CDS |
Nonsynonymous[Arg191Cys] |
725
..
725
|
G/A |
rs104894815
|
+ |
CDS |
Nonsynonymous[Val205Met] |
759
..
759
|
G/A |
rs104894809
|
+ |
CDS |
Nonsynonymous[Arg216Gln] |
764
..
764
|
G/T |
rs104894808
|
+ |
CDS |
Nonsynonymous[Asp218Tyr] |
765
..
765
|
A/G |
rs104894816
|
+ |
CDS |
Nonsynonymous[Asp218Gly] |
910
..
910
|
G/A |
rs184692721
|
+ |
CDS |
Synonymous[Thr266Thr] |
1054
..
1054
|
A/G |
rs150473615
|
+ |
CDS |
Synonymous[Lys314Lys] |
1093
..
1093
|
C/T |
rs138483498
|
+ |
CDS |
Synonymous[Ala327Ala] |
1142
..
1142
|
G/A |
rs141479621
|
+ |
CDS |
Nonsynonymous[Gly344Arg] |
1157
..
1157
|
G/A |
rs199710067
|
+ |
CDS |
Nonsynonymous[Val349Met] |
1158
..
1158
|
T/C |
rs146196033
|
+ |
CDS |
Nonsynonymous[Val349Ala] |
1179
..
1179
|
G/T |
rs202091014
|
+ |
CDS |
Nonsynonymous[Gly356Val] |
1214
..
1214
|
G/C |
rs137930427
|
+ |
CDS |
Nonsynonymous[Gly368Arg] |
1285
..
1285
|
G/A |
rs61735969
|
+ |
CDS |
Synonymous[Thr391Thr] |
1311
..
1311
|
C/G |
rs181400617
|
+ |
CDS |
Nonsynonymous[Pro400Arg] |
1333
..
1333
|
G/T |
rs111552375
|
+ |
CDS |
Synonymous[Val407Val] |
1342
..
1342
|
G/A |
rs201176390
|
+ |
CDS |
Synonymous[Pro410Pro] |
1355
..
1355
|
G/A |
rs144017862
|
+ |
3'UTR |
|
1415
..
1415
|
C/T |
rs1126581
|
+ |
3'UTR |
|
1432
..
1432
|
C/T |
rs1126582
|
+ |
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 |
|