Product Details

SNP ID
rs186435630
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:25966674 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTCTTTAAAAACCCAAGCCAAAAGC[A/G]ACTGAGGCAGGAGACATTCTGCTGT
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_006355.4 741 Missense Mutation CAA,CGA Q51R NP_006346.1
XM_005248799.4 741 Missense Mutation CAA,CGA Q51R XP_005248856.1
XM_005248800.4 741 Missense Mutation CAA,CGA Q51R XP_005248857.1
XM_017010175.1 741 Missense Mutation CAA,CGA Q51R XP_016865664.1

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