Single Nucleotide Polymorphism (SNP) and indel
|
| Location |
Variation |
dbSNP ID |
Strand |
CDS/UTR |
Translation |
|
233
..
233
|
G/A |
rs111465596
|
+ |
CDS |
Nonsynonymous[Ser78Asn] |
|
383
..
383
|
C/T |
rs76289268
|
+ |
CDS |
Nonsynonymous[Pro128Leu] |
|
557
..
557
|
G/T |
rs62378414
|
+ |
CDS |
Nonsynonymous[Ser186Ile] |
|
598
^
599
|
-/G/T |
rs36001111
|
+ |
CDS |
|
|
1195
..
1195
|
A/G |
rs77250251
|
+ |
CDS |
Nonsynonymous[Lys399Glu] |
|
1232
..
1232
|
C/A |
rs62623563
|
+ |
CDS |
Nonsynonymous[Thr411Lys] |
|
1332
..
1332
|
T/C |
rs78745319
|
+ |
CDS |
Synonymous[Asn444Asn] |
|
1530
..
1530
|
G/T |
rs3749778
|
- |
CDS |
Synonymous[Val510Val] |
|
1581
..
1581
|
A/G |
rs3749777
|
- |
CDS |
Synonymous[Thr527Thr] |
|
1759
..
1759
|
G/- |
rs36021732
|
+ |
CDS |
|
|
2046
..
2046
|
G/A |
rs73265820
|
+ |
CDS |
Synonymous[Thr682Thr] |
|
2294
..
2294
|
A/C |
rs114304577
|
+ |
CDS |
Nonsynonymous[Asn765Thr] |
|
2393
..
2393
|
C/A |
rs116608782
|
+ |
CDS |
Nonsynonymous[Pro798His] |
| 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 |
|