Product Details

SNP ID

rs10769932

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:8614792 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGATGGCAGGGACTGCCATGGAACA[C/G]AGCATATGGAAGGTATGGTTGCCAC

Phenotype

MIM: 612000

Polymorphism

C/G, Transversion 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	7852	UTR 3			NP_055633.1
XM_006718397.2	7852	UTR 3			XP_006718460.1
XM_006718398.3	7852	UTR 3			XP_006718461.1
XM_011520504.1	7852	UTR 3			XP_011518806.1
XM_011520507.2	7852	UTR 3			XP_011518809.1
XM_011520508.1	7852	UTR 3			XP_011518810.1
XM_011520509.1	7852	UTR 3			XP_011518811.1
XM_011520510.1	7852	UTR 3			XP_011518812.1
XM_011520511.1	7852	UTR 3			XP_011518813.1
XM_011520512.1	7852	UTR 3			XP_011518814.1
XM_011520513.1	7852	UTR 3			XP_011518815.1
XM_011520514.2	7852	UTR 3			XP_011518816.1
XM_011520515.1	7852	UTR 3			XP_011518817.1
XM_011520516.1	7852	UTR 3			XP_011518818.1
XM_011520517.2	7852	UTR 3			XP_011518819.1
XM_011520518.1	7852	UTR 3			XP_011518820.1
XM_011520519.1	7852	UTR 3			XP_011518821.1
XM_011520522.2	7852	UTR 3			XP_011518824.1
XM_011520523.2	7852	UTR 3			XP_011518825.1
XM_011520524.1	7852	Intron			XP_011518826.1
XM_011520525.1	7852	Intron			XP_011518827.1
XM_011520526.2	7852	UTR 3			XP_011518828.1
XM_011520527.1	7852	UTR 3			XP_011518829.1
XM_017018629.1	7852	UTR 3			XP_016874118.1
XM_017018630.1	7852	UTR 3			XP_016874119.1
XM_017018631.1	7852	UTR 3			XP_016874120.1

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