Product Details

SNP ID
rs144009035
Assay Type
Functionally tested
NCBI dbSNP Submissions
18
Location
Chr.1:228408415 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGAGGCTCCATCAGCATGACCGGG[G/T]TTAGGGCAGAGAAGGTGGATAAGTA
Phenotype
MIM: 607868 MIM: 606123
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
TRIM11 PubMed Links

Gene Details

Gene
TRIM11
Gene Name
tripartite motif containing 11
There are no transcripts associated with this gene.

Gene
TRIM17
Gene Name
tripartite motif containing 17
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001024940.2 2137 Missense Mutation AAC,ACC N407T NP_001020111.1
NM_001134855.1 2137 Intron NP_001128327.1
NM_016102.3 2137 Missense Mutation AAC,ACC N407T NP_057186.1
XM_006711779.2 2137 Missense Mutation AAC,ACC N407T XP_006711842.1
XM_011544209.2 2137 Missense Mutation AAC,ACC N407T XP_011542511.1
XM_011544210.2 2137 Missense Mutation AAC,ACC N407T XP_011542512.1
XM_011544211.2 2137 Missense Mutation AAC,ACC N380T XP_011542513.1
XM_017001418.1 2137 UTR 3 XP_016856907.1
XM_017001419.1 2137 UTR 3 XP_016856908.1

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