Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCGCCTCGGATTTGGGGGCTTCCTC[A/C]CTCGTGGCTTTCCGAAGGCTGCTGG
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611852 MIM: 603841 | |||||||||||||||||||||||
Literature Links: |
MRPL47 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) - 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 |
MRPL47 - mitochondrial ribosomal protein L47 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020409.2 | 129 | Intron | NP_065142.2 | |||
NM_177988.1 | 129 | Intron | NP_817125.1 |
NDUFB5 - NADH:ubiquinone oxidoreductase subunit B5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001199957.1 | 129 | Missense Mutation | ACT,CCT | T,P 34 | NP_001186886.1 | |
NM_001199958.1 | 129 | Missense Mutation | ACT,CCT | T,P 34 | NP_001186887.1 | |
NM_002492.3 | 129 | Missense Mutation | ACT,CCT | T,P 34 | NP_002483.1 |