Product Details
- SNP ID
-
rs58388611
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.15:76354114 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ACTGGCAGAGCTTCTGCAGCACTGT[C/G]GGGTGGCGGCCGGACTGCACGATCA
- Phenotype
-
MIM: 611611
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
SCAPER
PubMed Links
Gene Details
- Gene
- SCAPER
- Gene Name
- S-phase cyclin A associated protein in the ER
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001145923.1 |
3953 |
Silent Mutation |
CCC,CCG |
P1048P |
NP_001139395.1 |
| NM_020843.2 |
3953 |
Silent Mutation |
CCC,CCG |
P1294P |
NP_065894.2 |
| XM_005254417.2 |
3953 |
Silent Mutation |
CCC,CCG |
P1300P |
XP_005254474.1 |
| XM_005254419.2 |
3953 |
Silent Mutation |
CCC,CCG |
P1294P |
XP_005254476.1 |
| XM_011521650.1 |
3953 |
Silent Mutation |
CCC,CCG |
P1300P |
XP_011519952.1 |
| XM_011521652.2 |
3953 |
Silent Mutation |
CCC,CCG |
P1284P |
XP_011519954.1 |
| XM_011521653.2 |
3953 |
Silent Mutation |
CCC,CCG |
P1166P |
XP_011519955.1 |
| XM_011521654.2 |
3953 |
Silent Mutation |
CCC,CCG |
P1054P |
XP_011519956.1 |
| XM_011521656.2 |
3953 |
Silent Mutation |
CCC,CCG |
P680P |
XP_011519958.1 |
| XM_017022266.1 |
3953 |
Silent Mutation |
CCC,CCG |
P1325P |
XP_016877755.1 |
| XM_017022267.1 |
3953 |
Silent Mutation |
CCC,CCG |
P1319P |
XP_016877756.1 |
| XM_017022268.1 |
3953 |
Silent Mutation |
CCC,CCG |
P1300P |
XP_016877757.1 |
| XM_017022269.1 |
3953 |
Silent Mutation |
CCC,CCG |
P1294P |
XP_016877758.1 |
| XM_017022270.1 |
3953 |
Silent Mutation |
CCC,CCG |
P1294P |
XP_016877759.1 |
| XM_017022271.1 |
3953 |
Silent Mutation |
CCC,CCG |
P1273P |
XP_016877760.1 |
| XM_017022272.1 |
3953 |
Silent Mutation |
CCC,CCG |
P1248P |
XP_016877761.1 |
| XM_017022273.1 |
3953 |
Silent Mutation |
CCC,CCG |
P1160P |
XP_016877762.1 |
| XM_017022274.1 |
3953 |
Intron |
|
|
XP_016877763.1 |
| XM_017022275.1 |
3953 |
Silent Mutation |
CCC,CCG |
P1019P |
XP_016877764.1 |
| XM_017022276.1 |
3953 |
Silent Mutation |
CCC,CCG |
P1019P |
XP_016877765.1 |
| XM_017022277.1 |
3953 |
Silent Mutation |
CCC,CCG |
P1013P |
XP_016877766.1 |
| XM_017022278.1 |
3953 |
Silent Mutation |
CCC,CCG |
P1013P |
XP_016877767.1 |
| XM_017022279.1 |
3953 |
Intron |
|
|
XP_016877768.1 |
| XM_017022280.1 |
3953 |
Intron |
|
|
XP_016877769.1 |
| XM_017022281.1 |
3953 |
Intron |
|
|
XP_016877770.1 |
| XM_017022282.1 |
3953 |
Intron |
|
|
XP_016877771.1 |
| XM_017022283.1 |
3953 |
Intron |
|
|
XP_016877772.1 |
| XM_017022284.1 |
3953 |
Intron |
|
|
XP_016877773.1 |
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