Single Nucleotide Polymorphism (SNP) and indel
|
Location |
Variation |
dbSNP ID |
Strand |
CDS/UTR |
Translation |
32
..
32
|
A/G |
rs11546063
|
+ |
CDS |
Nonsynonymous[Asp10Gly] |
49
..
49
|
T/C |
rs441602
|
+ |
CDS |
Nonsynonymous[Ser16Pro] |
114
..
114
|
C/T |
rs11546062
|
+ |
CDS |
Synonymous[Ser37Ser] |
120
..
120
|
G/C |
rs3747638
|
+ |
CDS |
Synonymous[Leu39Leu] |
120
..
120
|
G/C |
rs200048221
|
- |
CDS |
Synonymous[Leu39Leu] |
169
..
169
|
C/A |
rs201820758
|
- |
CDS |
Nonsynonymous[Gln56Lys] |
198
..
198
|
T/C |
rs11546096
|
+ |
CDS |
Synonymous[Gly65Gly] |
203
..
203
|
A/G |
rs11546095
|
+ |
CDS |
Nonsynonymous[Asn67Ser] |
206
..
206
|
G/A |
rs200881242
|
- |
CDS |
Nonsynonymous[Arg68Gln] |
208
..
208
|
G/T |
rs199917475
|
- |
CDS |
Nonsynonymous[Ala69Ser] |
228
..
228
|
G/A |
rs11546093
|
+ |
CDS |
Synonymous[Arg75Arg] |
248
..
248
|
G/A |
rs11546092
|
+ |
CDS |
Nonsynonymous[Gly82Asp] |
267
..
267
|
A/G |
rs11546091
|
+ |
CDS |
Synonymous[Lys88Lys] |
272
..
272
|
G/C |
rs11546094
|
+ |
CDS |
Nonsynonymous[Ser90Thr] |
329
..
329
|
C/T |
rs191132964
|
- |
CDS |
Nonsynonymous[Pro109Leu] |
337
..
337
|
A/T |
rs188703994
|
- |
CDS |
Nonsynonymous[Thr112Ser] |
339
..
339
|
T/C |
rs114105515
|
- |
CDS |
Synonymous[Thr112Thr] |
340
..
340
|
T/G |
rs140799895
|
- |
CDS |
Nonsynonymous[Ser113Ala] |
341
..
341
|
C/T |
rs183927297
|
- |
CDS |
Nonsynonymous[Ser113Leu] |
343
..
343
|
G/C |
rs190985433
|
- |
CDS |
Nonsynonymous[Ala114Pro] |
362
..
362
|
G/C |
rs142632901
|
- |
CDS |
Nonsynonymous[Arg120Thr] |
367
..
367
|
A/G |
rs185692630
|
- |
CDS |
Nonsynonymous[Asn122Asp] |
369
..
369
|
C/T/G |
rs181580600
|
- |
CDS |
|
370
..
370
|
G/A |
rs190071209
|
- |
CDS |
|
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 |
|