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ACTTACAGCTGCTGCTCGACCCTTC[C/T]GGAGGCTAGAGGCTTCACGGGATCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
2 submissions
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Phenotype: |
MIM: 612805 | ||||||||||||||||||||
Literature Links: |
MIR6878 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | 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 |
MIR6878 - microRNA 6878 | ||||||
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There are no transcripts associated with this gene. |
TARS2 - threonyl-tRNA synthetase 2, mitochondrial (putative) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271895.1 | 636 | Missense Mutation | CGG,TGG | R,W 196 | NP_001258824.1 | |
NM_001271896.1 | 636 | Missense Mutation | CGG,TGG | R,W 196 | NP_001258825.1 | |
NM_025150.4 | 636 | Missense Mutation | CGG,TGG | R,W 196 | NP_079426.2 | |
XM_006711555.1 | 636 | Missense Mutation | CGG,TGG | R,W 196 | XP_006711618.1 | |
XM_006711556.1 | 636 | Missense Mutation | CGG,TGG | R,W 196 | XP_006711619.1 | |
XM_017002394.1 | 636 | Missense Mutation | CGG,TGG | R,W 196 | XP_016857883.1 | |
XM_017002395.1 | 636 | Missense Mutation | CGG,TGG | R,W 196 | XP_016857884.1 |