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CCGGCTTCTTCTCTGGGGTAGGGGT[A/G]GCCTCGCCCGGAAGCAAGGCCTCTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611975 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC102724691 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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LOC102724691 - uncharacterized LOC102724691 | ||||||
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There are no transcripts associated with this gene. |
MRPS9 - mitochondrial ribosomal protein S9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_182640.2 | 135 | Missense Mutation | AGC,GGC | S,G 23 | NP_872578.1 | |
XM_011511644.2 | 135 | Intron | XP_011509946.1 |