Product Details

SNP ID
rs138171902
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:25966583 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGAAGCCACCTGCTCCATCTGCCTG[A/G]GCCTGATGACGAACCCAGTAAGCAT
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
TRIM38 PubMed Links

Gene Details

Gene
TRIM38
Gene Name
tripartite motif containing 38
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_006355.4 650 Missense Mutation AGC,GGC S21G NP_006346.1
XM_005248799.4 650 Missense Mutation AGC,GGC S21G XP_005248856.1
XM_005248800.4 650 Missense Mutation AGC,GGC S21G XP_005248857.1
XM_017010175.1 650 Missense Mutation AGC,GGC S21G XP_016865664.1

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