Product Details

SNP ID
rs111998125
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.11:8617566 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTCTGAGCCCAGGAGGAGTTCAGAT[A/G]TATACATGGCTCCTGAGCCCTGGAC
Phenotype
MIM: 612000
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
TRIM66 PubMed Links

Gene Details

Gene
TRIM66
Gene Name
tripartite motif containing 66
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_014818.1 5078 UTR 3 NP_055633.1
XM_006718397.2 5078 UTR 3 XP_006718460.1
XM_006718398.3 5078 UTR 3 XP_006718461.1
XM_011520504.1 5078 UTR 3 XP_011518806.1
XM_011520507.2 5078 UTR 3 XP_011518809.1
XM_011520508.1 5078 UTR 3 XP_011518810.1
XM_011520509.1 5078 UTR 3 XP_011518811.1
XM_011520510.1 5078 UTR 3 XP_011518812.1
XM_011520511.1 5078 UTR 3 XP_011518813.1
XM_011520512.1 5078 UTR 3 XP_011518814.1
XM_011520513.1 5078 UTR 3 XP_011518815.1
XM_011520514.2 5078 UTR 3 XP_011518816.1
XM_011520515.1 5078 UTR 3 XP_011518817.1
XM_011520516.1 5078 UTR 3 XP_011518818.1
XM_011520517.2 5078 UTR 3 XP_011518819.1
XM_011520518.1 5078 UTR 3 XP_011518820.1
XM_011520519.1 5078 UTR 3 XP_011518821.1
XM_011520522.2 5078 UTR 3 XP_011518824.1
XM_011520523.2 5078 UTR 3 XP_011518825.1
XM_011520524.1 5078 Intron XP_011518826.1
XM_011520525.1 5078 Intron XP_011518827.1
XM_011520526.2 5078 UTR 3 XP_011518828.1
XM_011520527.1 5078 UTR 3 XP_011518829.1
XM_017018629.1 5078 UTR 3 XP_016874118.1
XM_017018630.1 5078 UTR 3 XP_016874119.1
XM_017018631.1 5078 UTR 3 XP_016874120.1

View Full Product Details