Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAGCTGGCGCCTACTATCCAGCCCA[A/C]GGGGTGCAGCAGTTTCCCACTGGCG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600495 | ||||||||||||||||||||
Literature Links: |
EIF4G1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
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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 |
EIF4G1 - eukaryotic translation initiation factor 4 gamma 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001194946.1 | 771 | Missense Mutation | CAA,CAC | Q,H 156 | NP_001181875.1 | |
NM_001194947.1 | 771 | Missense Mutation | CAA,CAC | Q,H 156 | NP_001181876.1 | |
NM_001291157.1 | 771 | Missense Mutation | CAA,CAC | Q,H 109 | NP_001278086.1 | |
NM_004953.4 | 771 | Intron | NP_004944.3 | |||
NM_182917.4 | 771 | Missense Mutation | CAA,CAC | Q,H 149 | NP_886553.3 | |
NM_198241.2 | 771 | Missense Mutation | CAA,CAC | Q,H 149 | NP_937884.1 | |
NM_198242.2 | 771 | UTR 5 | NP_937885.1 | |||
NM_198244.2 | 771 | Missense Mutation | CAA,CAC | Q,H 62 | NP_937887.1 |
SNORD66 - small nucleolar RNA, C/D box 66 | ||||||
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There are no transcripts associated with this gene. |