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CCGACACCGCCGATGCCAGGGCGCC[C/T]GTGGCCTCATCCGCCACTTCCAGGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 192150 MIM: 609693 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
VARS 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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VARS - valyl-tRNA synthetase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006295.2 | 3848 | Silent Mutation | ACA,ACG | T,T 1143 | NP_006286.1 | |
XM_005249362.2 | 3848 | Silent Mutation | ACA,ACG | T,T 1144 | XP_005249419.1 | |
XM_017011246.1 | 3848 | Silent Mutation | ACA,ACG | T,T 561 | XP_016866735.1 | |
XM_017011247.1 | 3848 | Silent Mutation | ACA,ACG | T,T 561 | XP_016866736.1 |
VWA7 - von Willebrand factor A domain containing 7 | ||||||
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There are no transcripts associated with this gene. |