Search
LOADING 
- SNP ID:
- rs143846565
- Gene
-
RPS6KA5 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.14: 90872089 - 90872089 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
CCTACCATGCCTAAGCTACTGAGTC[C/T]GAGAACTGGAAGAGGGTCTCCGGGT
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 603607
|
||||||||||||||||||||
Literature Links: |
RPS6KA5 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap |
|---|---|---|
| Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
| EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
| SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
| AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
| EUR - Not Available | ||
| AMR - Not Available |
| RPS6KA5 - ribosomal protein S6 kinase A5 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001322227.1 | 2501 | Silent Mutation | TCA,TCG | S,S 517 | NP_001309156.1 | |
| NM_001322228.1 | 2501 | Silent Mutation | TCA,TCG | S,S 762 | NP_001309157.1 | |
| NM_001322229.1 | 2501 | Silent Mutation | TCA,TCG | S,S 791 | NP_001309158.1 | |
| NM_001322230.1 | 2501 | Silent Mutation | TCA,TCG | S,S 531 | NP_001309159.1 | |
| NM_001322231.1 | 2501 | Silent Mutation | TCA,TCG | S,S 559 | NP_001309160.1 | |
| NM_001322232.1 | 2501 | Silent Mutation | TCA,TCG | S,S 725 | NP_001309161.1 | |
| NM_001322233.1 | 2501 | Silent Mutation | TCA,TCG | S,S 744 | NP_001309162.1 | |
| NM_001322234.1 | 2501 | Silent Mutation | TCA,TCG | S,S 606 | NP_001309163.1 | |
| NM_001322235.1 | 2501 | Silent Mutation | TCA,TCG | S,S 719 | NP_001309164.1 | |
| NM_001322236.1 | 2501 | Silent Mutation | TCA,TCG | S,S 770 | NP_001309165.1 | |
| NM_001322237.1 | 2501 | Silent Mutation | TCA,TCG | S,S 719 | NP_001309166.1 | |
| NM_001322238.1 | 2501 | Silent Mutation | TCA,TCG | S,S 579 | NP_001309167.1 | |
| NM_004755.3 | 2501 | Silent Mutation | TCA,TCG | S,S 798 | NP_004746.2 | |
| NM_182398.2 | 2501 | Intron | NP_872198.1 | |||
| XM_017021786.1 | 2501 | Silent Mutation | TCA,TCG | S,S 579 | XP_016877275.1 | |
Back To Top