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Search Thermo Fisher Scientific
ACTGGCAGAGCTTCTGCAGCACTGT[C/G]GGGTGGCGGCCGGACTGCACGATCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611611 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SCAPER PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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SCAPER - S-phase cyclin A associated protein in the ER | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145923.1 | 3953 | Silent Mutation | CCC,CCG | P,P 1048 | NP_001139395.1 | |
NM_020843.2 | 3953 | Silent Mutation | CCC,CCG | P,P 1294 | NP_065894.2 | |
XM_005254417.2 | 3953 | Silent Mutation | CCC,CCG | P,P 1300 | XP_005254474.1 | |
XM_005254419.2 | 3953 | Silent Mutation | CCC,CCG | P,P 1294 | XP_005254476.1 | |
XM_011521650.1 | 3953 | Silent Mutation | CCC,CCG | P,P 1300 | XP_011519952.1 | |
XM_011521652.2 | 3953 | Silent Mutation | CCC,CCG | P,P 1284 | XP_011519954.1 | |
XM_011521653.2 | 3953 | Silent Mutation | CCC,CCG | P,P 1166 | XP_011519955.1 | |
XM_011521654.2 | 3953 | Silent Mutation | CCC,CCG | P,P 1054 | XP_011519956.1 | |
XM_011521656.2 | 3953 | Silent Mutation | CCC,CCG | P,P 680 | XP_011519958.1 | |
XM_017022266.1 | 3953 | Silent Mutation | CCC,CCG | P,P 1325 | XP_016877755.1 | |
XM_017022267.1 | 3953 | Silent Mutation | CCC,CCG | P,P 1319 | XP_016877756.1 | |
XM_017022268.1 | 3953 | Silent Mutation | CCC,CCG | P,P 1300 | XP_016877757.1 | |
XM_017022269.1 | 3953 | Silent Mutation | CCC,CCG | P,P 1294 | XP_016877758.1 | |
XM_017022270.1 | 3953 | Silent Mutation | CCC,CCG | P,P 1294 | XP_016877759.1 | |
XM_017022271.1 | 3953 | Silent Mutation | CCC,CCG | P,P 1273 | XP_016877760.1 | |
XM_017022272.1 | 3953 | Silent Mutation | CCC,CCG | P,P 1248 | XP_016877761.1 | |
XM_017022273.1 | 3953 | Silent Mutation | CCC,CCG | P,P 1160 | XP_016877762.1 | |
XM_017022274.1 | 3953 | Intron | XP_016877763.1 | |||
XM_017022275.1 | 3953 | Silent Mutation | CCC,CCG | P,P 1019 | XP_016877764.1 | |
XM_017022276.1 | 3953 | Silent Mutation | CCC,CCG | P,P 1019 | XP_016877765.1 | |
XM_017022277.1 | 3953 | Silent Mutation | CCC,CCG | P,P 1013 | XP_016877766.1 | |
XM_017022278.1 | 3953 | Silent Mutation | CCC,CCG | P,P 1013 | 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 |