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CTCAAGTTTTGCAAGATGATTCTGT[C/T]GAACCCAAAATTTGCTGAACATGGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604601 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MTRF1 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
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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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MTRF1 - mitochondrial translational release factor 1 | ||||||
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There are no transcripts associated with this gene. |
NAA16 - N(alpha)-acetyltransferase 16, NatA auxiliary subunit | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001110798.1 | 413 | Missense Mutation | TCG,TTG | S,L 38 | NP_001104268.1 | |
NM_018527.3 | 413 | Missense Mutation | TCG,TTG | S,L 38 | NP_060997.2 | |
NM_024561.4 | 413 | Missense Mutation | TCG,TTG | S,L 38 | NP_078837.3 | |
XM_005266523.2 | 413 | Intron | XP_005266580.1 | |||
XM_006719866.2 | 413 | Missense Mutation | TCG,TTG | S,L 38 | XP_006719929.1 | |
XM_011535227.2 | 413 | Missense Mutation | TCG,TTG | S,L 38 | XP_011533529.1 | |
XM_011535228.1 | 413 | Missense Mutation | TCG,TTG | S,L 38 | XP_011533530.1 | |
XM_017020744.1 | 413 | Intron | XP_016876233.1 | |||
XM_017020745.1 | 413 | Missense Mutation | TCG,TTG | S,L 38 | XP_016876234.1 | |
XM_017020746.1 | 413 | Missense Mutation | TCG,TTG | S,L 38 | XP_016876235.1 |