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CGTGATGGACTCCGCCCTTTCTAGG[A/G]CGGTTTCTGGTTGATCTAGTCACAG
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611989 MIM: 615484 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
MRPS27 PubMed Links | |||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
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Global
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Caucasian - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | YRI (Yoruba) - Not Available | ||||||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | ||||||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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MRPS27 - mitochondrial ribosomal protein S27 | ||||||
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There are no transcripts associated with this gene. |
PTCD2 - pentatricopeptide repeat domain 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001284403.1 | Intron | NP_001271332.1 | ||||
NM_001284404.1 | Intron | NP_001271333.1 | ||||
NM_001284405.1 | Intron | NP_001271334.1 | ||||
NM_024754.4 | Intron | NP_079030.3 | ||||
XM_005248601.2 | Intron | XP_005248658.1 | ||||
XM_005248603.2 | Intron | XP_005248660.1 | ||||
XM_017009866.1 | Intron | XP_016865355.1 | ||||
XM_017009867.1 | Intron | XP_016865356.1 | ||||
XM_017009868.1 | Intron | XP_016865357.1 |