Product Details

SNP ID

rs58353604

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:8612861 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCAACTACAGCAGGCTCTAACTGGT[A/G]CAGGATCATGGTGAGGAGCTGCCCA

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	9783	UTR 3			NP_055633.1
XM_006718397.2	9783	UTR 3			XP_006718460.1
XM_006718398.3	9783	UTR 3			XP_006718461.1
XM_011520504.1	9783	UTR 3			XP_011518806.1
XM_011520507.2	9783	UTR 3			XP_011518809.1
XM_011520508.1	9783	UTR 3			XP_011518810.1
XM_011520509.1	9783	UTR 3			XP_011518811.1
XM_011520510.1	9783	UTR 3			XP_011518812.1
XM_011520511.1	9783	UTR 3			XP_011518813.1
XM_011520512.1	9783	UTR 3			XP_011518814.1
XM_011520513.1	9783	UTR 3			XP_011518815.1
XM_011520514.2	9783	UTR 3			XP_011518816.1
XM_011520515.1	9783	UTR 3			XP_011518817.1
XM_011520516.1	9783	UTR 3			XP_011518818.1
XM_011520517.2	9783	UTR 3			XP_011518819.1
XM_011520518.1	9783	UTR 3			XP_011518820.1
XM_011520519.1	9783	UTR 3			XP_011518821.1
XM_011520522.2	9783	UTR 3			XP_011518824.1
XM_011520523.2	9783	UTR 3			XP_011518825.1
XM_011520524.1	9783	Intron			XP_011518826.1
XM_011520525.1	9783	Intron			XP_011518827.1
XM_011520526.2	9783	UTR 3			XP_011518828.1
XM_011520527.1	9783	UTR 3			XP_011518829.1
XM_017018629.1	9783	UTR 3			XP_016874118.1
XM_017018630.1	9783	UTR 3			XP_016874119.1
XM_017018631.1	9783	UTR 3			XP_016874120.1

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