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TAGCTCCCTGTCTTGGATGAAGCCA[A/G]CAAACATCTGAGACTCCATAAAAAC
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 |
---|---|---|
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 |
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 | 3642 | Missense Mutation | GCT,GTT | A,V 1083 | NP_005409.3 | |
NM_139157.2 | 3642 | Missense Mutation | GCT,GTT | A,V 663 | NP_631896.1 | |
NM_213618.1 | 3642 | Missense Mutation | GCT,GTT | A,V 1083 | NP_998783.1 | |
XM_005253077.1 | 3642 | Missense Mutation | GCT,GTT | A,V 1113 | XP_005253134.1 | |
XM_005253083.2 | 3642 | Missense Mutation | GCT,GTT | A,V 663 | XP_005253140.1 | |
XM_011520309.1 | 3642 | Missense Mutation | GCT,GTT | A,V 1133 | XP_011518611.1 | |
XM_011520310.1 | 3642 | Missense Mutation | GCT,GTT | A,V 1123 | XP_011518612.1 | |
XM_011520311.2 | 3642 | Missense Mutation | GCT,GTT | A,V 1103 | XP_011518613.1 | |
XM_011520312.1 | 3642 | Missense Mutation | GCT,GTT | A,V 1103 | XP_011518614.1 | |
XM_011520313.1 | 3642 | Missense Mutation | GCT,GTT | A,V 1103 | XP_011518615.1 | |
XM_011520314.1 | 3642 | Missense Mutation | GCT,GTT | A,V 1103 | XP_011518616.1 | |
XM_011520315.1 | 3642 | Missense Mutation | GCT,GTT | A,V 1103 | XP_011518617.1 | |
XM_011520316.1 | 3642 | Missense Mutation | GCT,GTT | A,V 1103 | XP_011518618.1 | |
XM_011520317.1 | 3642 | Missense Mutation | GCT,GTT | A,V 1103 | XP_011518619.1 | |
XM_011520318.1 | 3642 | Missense Mutation | GCT,GTT | A,V 1083 | XP_011518620.1 | |
XM_011520319.2 | 3642 | Missense Mutation | GCT,GTT | A,V 923 | XP_011518621.1 | |
XM_011520320.1 | 3642 | Intron | XP_011518622.1 | |||
XM_011520321.2 | 3642 | Intron | XP_011518623.1 | |||
XM_011520322.1 | 3642 | Intron | XP_011518624.1 | |||
XM_011520323.2 | 3642 | Missense Mutation | GCT,GTT | A,V 713 | XP_011518625.2 | |
XM_011520324.2 | 3642 | Missense Mutation | GCT,GTT | A,V 693 | XP_011518626.2 | |
XM_011520325.1 | 3642 | Missense Mutation | GCT,GTT | A,V 683 | XP_011518627.1 | |
XM_011520326.1 | 3642 | Missense Mutation | GCT,GTT | A,V 683 | XP_011518628.1 | |
XM_011520327.1 | 3642 | Missense Mutation | GCT,GTT | A,V 683 | XP_011518629.1 | |
XM_011520328.1 | 3642 | Missense Mutation | GCT,GTT | A,V 683 | XP_011518630.1 | |
XM_011520329.1 | 3642 | Missense Mutation | GCT,GTT | A,V 663 | XP_011518631.1 | |
XM_017018182.1 | 3642 | Missense Mutation | GCT,GTT | A,V 1103 | XP_016873671.1 | |
XM_017018183.1 | 3642 | Missense Mutation | GCT,GTT | A,V 1103 | XP_016873672.1 | |
XM_017018184.1 | 3642 | Missense Mutation | GCT,GTT | A,V 923 | XP_016873673.1 | |
XM_017018185.1 | 3642 | Missense Mutation | GCT,GTT | A,V 923 | XP_016873674.1 | |
XM_017018186.1 | 3642 | Missense Mutation | GCT,GTT | A,V 903 | XP_016873675.1 | |
XM_017018187.1 | 3642 | Missense Mutation | GCT,GTT | A,V 683 | XP_016873676.1 |