Product Details

SNP ID
rs201155310
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:2360766 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCAGGAAGCAGATGGAATCGATTCG[G/T]TGATTGTAGTGGACAATGTCCCTCA
Phenotype
MIM: 603917 MIM: 614905
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
EIF3B PubMed Links

Gene Details

Gene
EIF3B
Gene Name
eukaryotic translation initiation factor 3 subunit B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001037283.1 821 Missense Mutation GTG,TTG V186L NP_001032360.1
NM_003751.3 821 Missense Mutation GTG,TTG V186L NP_003742.2
XM_011515599.1 821 Missense Mutation GTG,TTG V186L XP_011513901.1
XM_011515600.1 821 Missense Mutation GTG,TTG V186L XP_011513902.1
XM_011515601.1 821 Missense Mutation GTG,TTG V147L XP_011513903.1
XM_017012752.1 821 Missense Mutation GTG,TTG V186L XP_016868241.1
XM_017012753.1 821 Missense Mutation GTG,TTG V186L XP_016868242.1
Gene
SNX8
Gene Name
sorting nexin 8
There are no transcripts associated with this gene.

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