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GGTGGGGGCTCTCCTGGGCCCCTAC[A/G]CCTCTGGCTCATACTCCTGATATTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602569 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
EIF4E1B 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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EIF4E1B - eukaryotic translation initiation factor 4E family member 1B | ||||||
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There are no transcripts associated with this gene. |
MIR4281 - microRNA 4281 | ||||||
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There are no transcripts associated with this gene. |
SNCB - synuclein beta | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001001502.2 | 692 | Missense Mutation | GCG,GTG | A,V 134 | NP_001001502.1 | |
NM_001318034.1 | 692 | Missense Mutation | GCG,GTG | A,V 120 | NP_001304963.1 | |
NM_001318035.1 | 692 | Missense Mutation | GCG,GTG | A,V 104 | NP_001304964.1 | |
NM_001318036.1 | 692 | Missense Mutation | GCG,GTG | A,V 120 | NP_001304965.1 | |
NM_001318037.1 | 692 | Missense Mutation | GCG,GTG | A,V 104 | NP_001304966.1 | |
NM_003085.4 | 692 | Missense Mutation | GCG,GTG | A,V 134 | NP_003076.1 | |
XM_006714914.3 | 692 | Intron | XP_006714977.1 | |||
XM_006714915.3 | 692 | Intron | XP_006714978.1 | |||
XM_006714916.2 | 692 | Missense Mutation | GCG,GTG | A,V 134 | XP_006714979.1 | |
XM_011534640.2 | 692 | Intron | XP_011532942.1 |