Product Details

SNP ID
rs147508131
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.6:30186042 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGGGCGATGCCCACTCTCCGGGGC[C/G]GCAGTGCTGGGAAAAGCTCAGCCTC
Phenotype
MIM: 600830
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
TRIM26 PubMed Links

Gene Details

Gene
TRIM26
Gene Name
tripartite motif containing 26
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001242783.1 1584 Missense Mutation CCG,CGG P485R NP_001229712.1
NM_003449.4 1584 Missense Mutation CCG,CGG P485R NP_003440.1
XM_005249374.2 1584 Missense Mutation CCG,CGG P485R XP_005249431.1
XM_005249375.2 1584 Missense Mutation CCG,CGG P485R XP_005249432.1
XM_005249376.2 1584 Missense Mutation CCG,CGG P485R XP_005249433.1
XM_005249377.2 1584 Missense Mutation CCG,CGG P485R XP_005249434.1
XM_005249378.2 1584 Missense Mutation CCG,CGG P485R XP_005249435.1
XM_006715180.2 1584 Missense Mutation CCG,CGG P485R XP_006715243.1
XM_011514859.1 1584 Missense Mutation CCG,CGG P408R XP_011513161.1
XM_017011263.1 1584 Missense Mutation CCG,CGG P408R XP_016866752.1

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