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GCCAGGATACTTACTCCTTCACCAC[A/G]CGAATGCCCAGAGAACGGGCAGACC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611826 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MRPL11 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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MRPL11 - mitochondrial ribosomal protein L11 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_016050.4 | 556 | Silent Mutation | CGC,CGT | R,R 154 | NP_057134.1 | |
NM_170738.3 | 556 | Silent Mutation | CGC,CGT | R,R 128 | NP_733934.1 | |
NM_170739.3 | 556 | Silent Mutation | CGC,CGT | R,R 154 | NP_733935.1 | |
XM_017018135.1 | 556 | Silent Mutation | CGC,CGT | R,R 128 | XP_016873624.1 |