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Search Thermo Fisher Scientific
GGGTCGCATGCTGAGCCCCCTGTCC[C/T]GGCACAGGGCGAGGCCCCAGGAGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603917 MIM: 614905 | ||||||||||||||||||||
Literature Links: |
EIF3B PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
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 |
EIF3B - eukaryotic translation initiation factor 3 subunit B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001037283.1 | 687 | Missense Mutation | CCG,CTG | P,L 102 | NP_001032360.1 | |
NM_003751.3 | 687 | Missense Mutation | CCG,CTG | P,L 102 | NP_003742.2 | |
XM_011515599.1 | 687 | Missense Mutation | CCG,CTG | P,L 102 | XP_011513901.1 | |
XM_011515600.1 | 687 | Missense Mutation | CCG,CTG | P,L 102 | XP_011513902.1 | |
XM_011515601.1 | 687 | Intron | XP_011513903.1 | |||
XM_017012752.1 | 687 | Missense Mutation | CCG,CTG | P,L 102 | XP_016868241.1 | |
XM_017012753.1 | 687 | Missense Mutation | CCG,CTG | P,L 102 | XP_016868242.1 |
SNX8 - sorting nexin 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_013321.3 | 687 | Intron | NP_037453.1 | |||
XM_011515329.2 | 687 | Intron | XP_011513631.1 | |||
XM_011515330.1 | 687 | Intron | XP_011513632.1 | |||
XM_017012083.1 | 687 | Intron | XP_016867572.1 | |||
XM_017012084.1 | 687 | Intron | XP_016867573.1 |