Single Nucleotide Polymorphism (SNP) and indel
|
| Location |
Variation |
dbSNP ID |
Strand |
CDS/UTR |
Translation |
|
41
..
41
|
G/T |
rs61760186
|
- |
CDS |
Nonsynonymous[Cys6Phe] |
|
140
..
140
|
A/G |
rs117801409
|
- |
CDS |
Nonsynonymous[Asp39Gly] |
|
185
..
185
|
T/G |
rs35306604
|
- |
CDS |
Nonsynonymous[Met54Arg] |
|
199
..
199
|
A/G |
rs35744230
|
- |
CDS |
Nonsynonymous[Asn59Asp] |
|
290
..
290
|
A/G |
rs61757564
|
- |
CDS |
Nonsynonymous[Asn89Ser] |
|
384
..
384
|
T/C |
rs11559069
|
+ |
CDS |
Synonymous[Asn120Asn] |
|
474
..
474
|
A/C |
rs3212230
|
+ |
CDS |
Synonymous[Leu150Leu] |
|
520
..
520
|
A/G |
rs35977478
|
- |
CDS |
Nonsynonymous[Ser166Gly] |
|
651
..
651
|
A/G |
rs116421328
|
- |
CDS |
Synonymous[Leu209Leu] |
|
666
..
666
|
C/T |
rs1129644
|
+ |
CDS |
Synonymous[Asn214Asn] |
|
759
..
759
|
A/G |
rs11559067
|
+ |
CDS |
Synonymous[Leu245Leu] |
|
769
..
769
|
C/G |
rs2294689
|
+ |
CDS |
Nonsynonymous[Gln249Glu] |
|
827
..
827
|
G/A |
rs17249952
|
+ |
CDS |
Nonsynonymous[Arg268Gln] |
|
943
..
943
|
A/G |
rs77273535
|
- |
CDS |
Nonsynonymous[Ile307Val] |
|
1145
..
1145
|
T/G |
rs17249973
|
+ |
3'UTR |
|
|
1185
..
1185
|
G/T |
rs77370926
|
- |
3'UTR |
|
|
1205
..
1205
|
C/A |
rs11754730
|
- |
3'UTR |
|
|
1368
..
1368
|
T/C |
rs3087943
|
- |
3'UTR |
|
|
1398
..
1398
|
A/C |
rs1047782
|
+ |
3'UTR |
|
|
1413
..
1413
|
T/C |
rs17249980
|
+ |
3'UTR |
|
|
1458
..
1458
|
G/A |
rs707887
|
+ |
3'UTR |
|
|
1503
..
1503
|
G/A |
rs16889567
|
- |
3'UTR |
|
|
1872
..
1872
|
A/- |
rs66564743
|
- |
3'UTR |
|
|
1892
..
1892
|
A/G |
rs12393
|
- |
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 |
|