Single Nucleotide Polymorphism (SNP) and indel
|
Location |
Variation |
dbSNP ID |
Strand |
CDS/UTR |
Translation |
122
..
122
|
C/A |
rs61746898
|
+ |
CDS |
Synonymous[Ser33Ser] |
173
..
173
|
C/T |
rs149786271
|
+ |
CDS |
Synonymous[Ser50Ser] |
223
..
223
|
A/G |
rs147909337
|
+ |
CDS |
Nonsynonymous[Glu67Gly] |
250
..
250
|
C/A |
rs41291916
|
+ |
CDS |
Nonsynonymous[Pro76Gln] |
278
..
278
|
C/T |
rs35052255
|
- |
CDS |
Synonymous[Cys85Cys] |
301
..
301
|
G/A |
rs144386388
|
+ |
CDS |
Nonsynonymous[Gly93Glu] |
366
..
366
|
C/G |
rs201818972
|
+ |
CDS |
Nonsynonymous[Pro115Ala] |
372
..
372
|
T/C |
rs201416763
|
+ |
CDS |
Nonsynonymous[Cys117Arg] |
404
..
404
|
G/T |
rs199605610
|
+ |
CDS |
Synonymous[Gly127Gly] |
405
..
405
|
C/G |
rs147836127
|
+ |
CDS |
Nonsynonymous[Pro128Ala] |
430
..
430
|
T/G |
rs141428040
|
+ |
CDS |
Nonsynonymous[Met136Arg] |
438
..
438
|
C/T |
rs147838633
|
+ |
CDS |
Nonsynonymous[Arg139Cys] |
464
..
464
|
T/C |
rs13194610
|
+ |
CDS |
Synonymous[Asn147Asn] |
490
..
490
|
C/A |
rs200640805
|
+ |
CDS |
Nonsynonymous[Pro156Gln] |
940
..
940
|
G/T |
rs143287461
|
+ |
CDS |
Nonsynonymous[Arg306Leu] |
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 |
|