Product Details

SNP ID
rs139179327
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:115126578 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTGAATTCCTCCACTGCCCATTAA[G/T]GCAAATGCTGGATACAGTGTATGTG
Phenotype
MIM: 609317
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
TRIM36 PubMed Links

Gene Details

Gene
TRIM36
Gene Name
tripartite motif containing 36
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001017397.1 2633 Intron NP_001017397.1
NM_001017398.1 2633 Intron NP_001017398.1
NM_001300752.1 2633 Silent Mutation NP_001287681.1
NM_001300759.1 2633 Silent Mutation NP_001287688.1
NM_018700.3 2633 Silent Mutation NP_061170.2
XM_017009621.1 2633 Silent Mutation XP_016865110.1
XM_017009622.1 2633 Silent Mutation XP_016865111.1
XM_017009623.1 2633 Intron XP_016865112.1

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