Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601065 MIM: 605812 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
AARS 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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AARS - alanyl-tRNA synthetase | ||||||
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There are no transcripts associated with this gene. |
DDX19B - DEAD-box helicase 19B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001014449.2 | 44 | Intron | NP_001014449.1 | |||
NM_001014451.2 | 44 | Intron | NP_001014451.1 | |||
NM_001257172.1 | 44 | Missense Mutation | CGC,TGC | R,C 11 | NP_001244101.1 | |
NM_001257173.1 | 44 | UTR 5 | NP_001244102.1 | |||
NM_001257174.1 | 44 | Intron | NP_001244103.1 | |||
NM_001257175.1 | 44 | Intron | NP_001244104.1 | |||
NM_007242.5 | 44 | Intron | NP_009173.1 | |||
XM_006721127.2 | 44 | Intron | XP_006721190.1 | |||
XM_011522832.2 | 44 | Missense Mutation | CGC,TGC | R,C 11 | XP_011521134.1 | |
XM_011522833.2 | 44 | Missense Mutation | CGC,TGC | R,C 11 | XP_011521135.1 | |
XM_011522834.2 | 44 | Missense Mutation | CGC,TGC | R,C 11 | XP_011521136.1 | |
XM_017022890.1 | 44 | UTR 5 | XP_016878379.1 |