Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603892 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
EFTUD2 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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EFTUD2 - elongation factor Tu GTP binding domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001142605.1 | 4236 | UTR 3 | NP_001136077.1 | |||
NM_001258353.1 | 4236 | UTR 3 | NP_001245282.1 | |||
NM_001258354.1 | 4236 | UTR 3 | NP_001245283.1 | |||
NM_004247.3 | 4236 | UTR 3 | NP_004238.3 |
HIGD1B - HIG1 hypoxia inducible domain family member 1B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271880.1 | 4236 | Missense Mutation | AAT,GAT | N,D 87 | NP_001258809.1 | |
NM_016438.3 | 4236 | Missense Mutation | AAT,GAT | N,D 87 | NP_057522.1 | |
XM_006721946.2 | 4236 | Missense Mutation | AAT,GAT | N,D 87 | XP_006722009.1 | |
XM_006721947.3 | 4236 | Missense Mutation | AAT,GAT | N,D 87 | XP_006722010.1 | |
XM_006721948.3 | 4236 | Missense Mutation | AAT,GAT | N,D 87 | XP_006722011.1 | |
XM_011524891.2 | 4236 | Missense Mutation | AAT,GAT | N,D 87 | XP_011523193.1 | |
XM_017024742.1 | 4236 | Missense Mutation | AAT,GAT | N,D 87 | XP_016880231.1 | |
XM_017024743.1 | 4236 | Missense Mutation | AAT,GAT | N,D 87 | XP_016880232.1 |
Set Membership: |
HapMap |