Single Nucleotide Polymorphism (SNP) and indel
|
Location |
Variation |
dbSNP ID |
Strand |
CDS/UTR |
Translation |
10
..
10
|
C/G |
rs167203
|
+ |
5'UTR |
|
14
..
14
|
T/C |
rs150285449
|
- |
5'UTR |
|
48
..
48
|
C/T |
rs111648912
|
- |
5'UTR |
|
56
..
56
|
A/G |
rs11548842
|
+ |
5'UTR |
|
63
..
63
|
T/A |
rs138667733
|
- |
5'UTR |
|
69
..
69
|
A/G |
rs202064506
|
- |
CDS |
Synonymous[Glu2Glu] |
79
..
79
|
C/T |
rs150076109
|
- |
CDS |
Nonsynonymous[Pro6Ser] |
108
..
108
|
C/T |
rs199952772
|
- |
CDS |
Synonymous[Thr15Thr] |
135
..
135
|
A/C |
rs114536498
|
- |
CDS |
Synonymous[Ala24Ala] |
138
..
138
|
A/G |
rs11548845
|
+ |
CDS |
Synonymous[Glu25Glu] |
306
..
306
|
C/T |
rs201251896
|
- |
CDS |
Synonymous[Ser81Ser] |
384
..
384
|
C/T |
rs11548846
|
+ |
CDS |
Synonymous[Thr107Thr] |
449
..
449
|
C/G |
rs140707980
|
- |
CDS |
Nonsynonymous[Ala129Gly] |
498
..
498
|
C/T |
rs116557087
|
- |
CDS |
Synonymous[Cys145Cys] |
582
..
582
|
C/T |
rs143811423
|
- |
CDS |
Synonymous[Asn173Asn] |
591
..
591
|
C/G |
rs201881795
|
- |
CDS |
Synonymous[Thr176Thr] |
656
..
656
|
A/G |
rs111725016
|
- |
CDS |
Nonsynonymous[Lys198Arg] |
753
..
753
|
C/T |
rs200783060
|
- |
CDS |
Synonymous[Tyr230Tyr] |
1047
..
1047
|
A/G |
rs140679593
|
- |
CDS |
Synonymous[Arg328Arg] |
1125
..
1125
|
A/T |
rs114279043
|
- |
CDS |
Synonymous[Pro354Pro] |
1165
..
1165
|
G/C |
rs182293768
|
- |
CDS |
Nonsynonymous[Gly368Arg] |
1182
..
1182
|
T/C |
rs143712714
|
- |
CDS |
Synonymous[Tyr373Tyr] |
1203
..
1203
|
T/C |
rs181141777
|
- |
CDS |
Synonymous[Tyr380Tyr] |
1269
..
1269
|
T/C |
rs115527397
|
- |
CDS |
Synonymous[Ile402Ile] |
1299
..
1299
|
A/G |
rs61755088
|
- |
CDS |
Synonymous[Gln412Gln] |
1353
..
1353
|
C/T |
rs115346013
|
- |
CDS |
Synonymous[Ser430Ser] |
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 |
|