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CTGCCACGGCCAGCTTGTAGCGAGC[A/G]GTGTTCATGCCCGCGCTGCGGCGCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
3 submissions
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Phenotype: |
MIM: 604733 | ||||||||||||||||||||
Literature Links: |
WARS2 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 |
WARS2 - tryptophanyl tRNA synthetase 2, mitochondrial | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015836.3 | 747 | Silent Mutation | ACC,ACT | T,T 299 | NP_056651.1 | |
NM_201263.2 | 747 | UTR 3 | NP_957715.1 | |||
XM_005270350.3 | 747 | Silent Mutation | ACC,ACT | T,T 281 | XP_005270407.1 | |
XM_011540494.2 | 747 | Silent Mutation | ACC,ACT | T,T 276 | XP_011538796.1 | |
XM_011540495.2 | 747 | Silent Mutation | ACC,ACT | T,T 213 | XP_011538797.1 | |
XM_017000038.1 | 747 | Silent Mutation | ACC,ACT | T,T 280 | XP_016855527.1 | |
XM_017000039.1 | 747 | Silent Mutation | ACC,ACT | T,T 276 | XP_016855528.1 | |
XM_017000040.1 | 747 | Silent Mutation | ACC,ACT | T,T 242 | XP_016855529.1 | |
XM_017000041.1 | 747 | Silent Mutation | ACC,ACT | T,T 186 | XP_016855530.1 | |
XM_017000042.1 | 747 | UTR 3 | XP_016855531.1 |