Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTTGATCAAGTTTTACTATCGATGC[C/T]TGTAGTGCATAAAGTGCTTGCAGTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
3 submissions
|
||||||||||||||||||||
Phenotype: |
MIM: 603929 | ||||||||||||||||||||
Literature Links: |
EIF4G3 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
EIF4G3 - eukaryotic translation initiation factor 4 gamma 3 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001198801.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1551 | NP_001185730.1 | |
NM_001198802.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1521 | NP_001185731.1 | |
NM_001198803.2 | 5653 | Intron | NP_001185732.1 | |||
NM_003760.4 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1515 | NP_003751.2 | |
XM_011542356.2 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1607 | XP_011540658.1 | |
XM_011542361.2 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1570 | XP_011540663.1 | |
XM_011542370.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1608 | XP_011540672.1 | |
XM_011542371.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1563 | XP_011540673.1 | |
XM_011542374.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1552 | XP_011540676.1 | |
XM_011542375.2 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1552 | XP_011540677.1 | |
XM_011542381.2 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1067 | XP_011540683.1 | |
XM_017002672.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1608 | XP_016858161.1 | |
XM_017002673.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1601 | XP_016858162.1 | |
XM_017002674.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1600 | XP_016858163.1 | |
XM_017002675.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1597 | XP_016858164.1 | |
XM_017002676.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1590 | XP_016858165.1 | |
XM_017002677.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1590 | XP_016858166.1 | |
XM_017002678.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1571 | XP_016858167.1 | |
XM_017002679.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1570 | XP_016858168.1 | |
XM_017002680.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1570 | XP_016858169.1 | |
XM_017002681.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1569 | XP_016858170.1 | |
XM_017002682.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1563 | XP_016858171.1 | |
XM_017002683.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1563 | XP_016858172.1 | |
XM_017002684.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1563 | XP_016858173.1 | |
XM_017002685.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1560 | XP_016858174.1 | |
XM_017002686.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1559 | XP_016858175.1 | |
XM_017002687.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1559 | XP_016858176.1 | |
XM_017002688.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1559 | XP_016858177.1 | |
XM_017002689.1 | 5653 | Intron | XP_016858178.1 | |||
XM_017002690.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1558 | XP_016858179.1 | |
XM_017002691.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1553 | XP_016858180.1 | |
XM_017002692.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1552 | XP_016858181.1 | |
XM_017002693.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1552 | XP_016858182.1 | |
XM_017002694.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1533 | XP_016858183.1 | |
XM_017002695.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1532 | XP_016858184.1 | |
XM_017002696.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1526 | XP_016858185.1 | |
XM_017002697.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1525 | XP_016858186.1 | |
XM_017002698.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1522 | XP_016858187.1 | |
XM_017002699.1 | 5653 | Intron | XP_016858188.1 | |||
XM_017002700.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1515 | XP_016858189.1 | |
XM_017002701.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1514 | XP_016858190.1 | |
XM_017002702.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1492 | XP_016858191.1 | |
XM_017002703.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1467 | XP_016858192.1 | |
XM_017002704.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1466 | XP_016858193.1 | |
XM_017002705.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1328 | XP_016858194.1 | |
XM_017002706.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1291 | XP_016858195.1 | |
XM_017002707.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1272 | XP_016858196.1 | |
XM_017002708.1 | 5653 | Silent Mutation | CAA,CAG | Q,Q 1235 | XP_016858197.1 | |
XM_017002709.1 | 5653 | Intron | XP_016858198.1 | |||
XM_017002710.1 | 5653 | Intron | XP_016858199.1 | |||
XM_017002711.1 | 5653 | Intron | XP_016858200.1 | |||
XM_017002712.1 | 5653 | Intron | XP_016858201.1 |