Product Details

SNP ID
rs144475271
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:30186257 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CATCGCCCAACGATTCCTCATCTTC[A/G]TCCGTTTCCCAGTCGTCATATCCAT
Phenotype
MIM: 600830
Polymorphism
A/G, Transition 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 1369 Silent Mutation NP_001229712.1
NM_003449.4 1369 Silent Mutation NP_003440.1
XM_005249374.2 1369 Silent Mutation XP_005249431.1
XM_005249375.2 1369 Silent Mutation XP_005249432.1
XM_005249376.2 1369 Silent Mutation XP_005249433.1
XM_005249377.2 1369 Silent Mutation XP_005249434.1
XM_005249378.2 1369 Silent Mutation XP_005249435.1
XM_006715180.2 1369 Silent Mutation XP_006715243.1
XM_011514859.1 1369 Silent Mutation XP_011513161.1
XM_017011263.1 1369 Silent Mutation XP_016866752.1

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