Product Details

SNP ID
rs144761656
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:27287618 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATGCGCAAAGGCTCTGGAGGCCCGG[C/T]GCCCCGTGCACCCCCCAGGTAGAAG
Phenotype
MIM: 617007
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
TRIM35 PubMed Links

Gene Details

Gene
TRIM35
Gene Name
tripartite motif containing 35
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001304495.1 1526 UTR 3 NP_001291424.1
NM_171982.4 1526 Missense Mutation ACC,GCC T472A NP_741983.2
XM_005273452.3 1526 UTR 3 XP_005273509.1
XM_011544453.1 1526 Missense Mutation ACC,GCC T322A XP_011542755.1

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