Product Details

SNP ID
rs147544193
Assay Type
Functionally Tested
NCBI dbSNP Submissions
2
Location
Chr.1:20817509 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTTTGAAAGTGCTTCAGAGGAACA[A/G]GGACTGTCAGACTCTATGAAGTCCA
Phenotype
MIM: 603929
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
EIF4G3 PubMed Links

Gene Details

Gene
EIF4G3
Gene Name
eukaryotic translation initiation factor 4 gamma 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001198801.1 5338 Silent Mutation NP_001185730.1
NM_001198802.1 5338 Silent Mutation NP_001185731.1
NM_001198803.2 5338 Intron NP_001185732.1
NM_003760.4 5338 Silent Mutation NP_003751.2
XM_011542356.2 5338 Silent Mutation XP_011540658.1
XM_011542361.2 5338 Silent Mutation XP_011540663.1
XM_011542370.1 5338 Silent Mutation XP_011540672.1
XM_011542371.1 5338 Silent Mutation XP_011540673.1
XM_011542374.1 5338 Silent Mutation XP_011540676.1
XM_011542375.2 5338 Silent Mutation XP_011540677.1
XM_011542381.2 5338 Silent Mutation XP_011540683.1
XM_017002672.1 5338 Silent Mutation XP_016858161.1
XM_017002673.1 5338 Silent Mutation XP_016858162.1
XM_017002674.1 5338 Silent Mutation XP_016858163.1
XM_017002675.1 5338 Silent Mutation XP_016858164.1
XM_017002676.1 5338 Silent Mutation XP_016858165.1
XM_017002677.1 5338 Silent Mutation XP_016858166.1
XM_017002678.1 5338 Silent Mutation XP_016858167.1
XM_017002679.1 5338 Silent Mutation XP_016858168.1
XM_017002680.1 5338 Silent Mutation XP_016858169.1
XM_017002681.1 5338 Silent Mutation XP_016858170.1
XM_017002682.1 5338 Silent Mutation XP_016858171.1
XM_017002683.1 5338 Silent Mutation XP_016858172.1
XM_017002684.1 5338 Silent Mutation XP_016858173.1
XM_017002685.1 5338 Silent Mutation XP_016858174.1
XM_017002686.1 5338 Silent Mutation XP_016858175.1
XM_017002687.1 5338 Silent Mutation XP_016858176.1
XM_017002688.1 5338 Silent Mutation XP_016858177.1
XM_017002689.1 5338 Silent Mutation XP_016858178.1
XM_017002690.1 5338 Silent Mutation XP_016858179.1
XM_017002691.1 5338 Silent Mutation XP_016858180.1
XM_017002692.1 5338 Silent Mutation XP_016858181.1
XM_017002693.1 5338 Silent Mutation XP_016858182.1
XM_017002694.1 5338 Silent Mutation XP_016858183.1
XM_017002695.1 5338 Silent Mutation XP_016858184.1
XM_017002696.1 5338 Silent Mutation XP_016858185.1
XM_017002697.1 5338 Silent Mutation XP_016858186.1
XM_017002698.1 5338 Silent Mutation XP_016858187.1
XM_017002699.1 5338 Silent Mutation XP_016858188.1
XM_017002700.1 5338 Silent Mutation XP_016858189.1
XM_017002701.1 5338 Silent Mutation XP_016858190.1
XM_017002702.1 5338 Silent Mutation XP_016858191.1
XM_017002703.1 5338 Silent Mutation XP_016858192.1
XM_017002704.1 5338 Silent Mutation XP_016858193.1
XM_017002705.1 5338 Silent Mutation XP_016858194.1
XM_017002706.1 5338 Silent Mutation XP_016858195.1
XM_017002707.1 5338 Silent Mutation XP_016858196.1
XM_017002708.1 5338 Silent Mutation XP_016858197.1
XM_017002709.1 5338 Silent Mutation XP_016858198.1
XM_017002710.1 5338 Intron XP_016858199.1
XM_017002711.1 5338 Intron XP_016858200.1
XM_017002712.1 5338 Intron XP_016858201.1

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