Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CATCTACGAGACTGTGCGGGACCGT[A/G]TGGCCAAGGGCAGCCAGGGGCCTCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602375 MIM: 606794 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MRPL12 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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MRPL12 - mitochondrial ribosomal protein L12 | ||||||
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There are no transcripts associated with this gene. |
SLC25A10 - solute carrier family 25 member 10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001270888.1 | 602 | Missense Mutation | ATG,GTG | M,V 89 | NP_001257817.1 | |
NM_001270953.1 | 602 | Missense Mutation | ATG,GTG | M,V 89 | NP_001257882.1 | |
NM_012140.4 | 602 | Missense Mutation | ATG,GTG | M,V 89 | NP_036272.2 | |
XM_017024220.1 | 602 | Missense Mutation | ATG,GTG | M,V 46 | XP_016879709.1 |