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GGCGGATGCTTTTGGAGGCCACAGA[C/T]TTGCGGAAGGCCTCTCGCTGAAAGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603637 MIM: 140750 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RPL27A PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
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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RPL27A - ribosomal protein L27a | ||||||
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There are no transcripts associated with this gene. |
ST5 - suppression of tumorigenicity 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005418.3 | 3580 | Silent Mutation | AAA,AAG | K,K 1062 | NP_005409.3 | |
NM_139157.2 | 3580 | Silent Mutation | AAA,AAG | K,K 642 | NP_631896.1 | |
NM_213618.1 | 3580 | Silent Mutation | AAA,AAG | K,K 1062 | NP_998783.1 | |
XM_005253077.1 | 3580 | Silent Mutation | AAA,AAG | K,K 1092 | XP_005253134.1 | |
XM_005253083.2 | 3580 | Silent Mutation | AAA,AAG | K,K 642 | XP_005253140.1 | |
XM_011520309.1 | 3580 | Silent Mutation | AAA,AAG | K,K 1112 | XP_011518611.1 | |
XM_011520310.1 | 3580 | Silent Mutation | AAA,AAG | K,K 1102 | XP_011518612.1 | |
XM_011520311.2 | 3580 | Silent Mutation | AAA,AAG | K,K 1082 | XP_011518613.1 | |
XM_011520312.1 | 3580 | Silent Mutation | AAA,AAG | K,K 1082 | XP_011518614.1 | |
XM_011520313.1 | 3580 | Silent Mutation | AAA,AAG | K,K 1082 | XP_011518615.1 | |
XM_011520314.1 | 3580 | Silent Mutation | AAA,AAG | K,K 1082 | XP_011518616.1 | |
XM_011520315.1 | 3580 | Silent Mutation | AAA,AAG | K,K 1082 | XP_011518617.1 | |
XM_011520316.1 | 3580 | Silent Mutation | AAA,AAG | K,K 1082 | XP_011518618.1 | |
XM_011520317.1 | 3580 | Silent Mutation | AAA,AAG | K,K 1082 | XP_011518619.1 | |
XM_011520318.1 | 3580 | Silent Mutation | AAA,AAG | K,K 1062 | XP_011518620.1 | |
XM_011520319.2 | 3580 | Silent Mutation | AAA,AAG | K,K 902 | XP_011518621.1 | |
XM_011520320.1 | 3580 | Intron | XP_011518622.1 | |||
XM_011520321.2 | 3580 | Intron | XP_011518623.1 | |||
XM_011520322.1 | 3580 | Intron | XP_011518624.1 | |||
XM_011520323.2 | 3580 | Silent Mutation | AAA,AAG | K,K 692 | XP_011518625.2 | |
XM_011520324.2 | 3580 | Silent Mutation | AAA,AAG | K,K 672 | XP_011518626.2 | |
XM_011520325.1 | 3580 | Silent Mutation | AAA,AAG | K,K 662 | XP_011518627.1 | |
XM_011520326.1 | 3580 | Silent Mutation | AAA,AAG | K,K 662 | XP_011518628.1 | |
XM_011520327.1 | 3580 | Silent Mutation | AAA,AAG | K,K 662 | XP_011518629.1 | |
XM_011520328.1 | 3580 | Silent Mutation | AAA,AAG | K,K 662 | XP_011518630.1 | |
XM_011520329.1 | 3580 | Silent Mutation | AAA,AAG | K,K 642 | XP_011518631.1 | |
XM_017018182.1 | 3580 | Silent Mutation | AAA,AAG | K,K 1082 | XP_016873671.1 | |
XM_017018183.1 | 3580 | Silent Mutation | AAA,AAG | K,K 1082 | XP_016873672.1 | |
XM_017018184.1 | 3580 | Silent Mutation | AAA,AAG | K,K 902 | XP_016873673.1 | |
XM_017018185.1 | 3580 | Silent Mutation | AAA,AAG | K,K 902 | XP_016873674.1 | |
XM_017018186.1 | 3580 | Silent Mutation | AAA,AAG | K,K 882 | XP_016873675.1 | |
XM_017018187.1 | 3580 | Silent Mutation | AAA,AAG | K,K 662 | XP_016873676.1 |