Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 191050 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
WARS 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)
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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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WARS - tryptophanyl-tRNA synthetase | ||||||
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There are no transcripts associated with this gene. |
WDR25 - WD repeat domain 25 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001161476.1 | 362 | Missense Mutation | CGG,TGG | R,W 88 | NP_001154948.1 | |
NM_024515.4 | 362 | Missense Mutation | CGG,TGG | R,W 88 | NP_078791.3 | |
XM_005268056.4 | 362 | Missense Mutation | CGG,TGG | R,W 88 | XP_005268113.1 | |
XM_005268057.3 | 362 | Intron | XP_005268114.1 | |||
XM_005268058.4 | 362 | Intron | XP_005268115.1 | |||
XM_011537150.2 | 362 | Missense Mutation | CGG,TGG | R,W 88 | XP_011535452.1 | |
XM_011537151.2 | 362 | Intron | XP_011535453.2 | |||
XM_017021639.1 | 362 | Intron | XP_016877128.1 |
Set Membership: |
HapMap |