Product Details

SNP ID
rs143397084
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:188091699 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTCTCTCCGGAAGCTCTGGCCGTGC[C/T]GCCCTTCGCGTCTGCAGAGCCGTGG
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
TRIML2 PubMed Links

Gene Details

Gene
TRIML2
Gene Name
tripartite motif family like 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001303419.1 1282 Missense Mutation AGC,GGC S355G NP_001290348.1
NM_173553.2 1282 UTR 3 NP_775824.2
XM_011531737.2 1282 Missense Mutation AGC,GGC S330G XP_011530039.1
XM_011531738.1 1282 Missense Mutation AGC,GGC S330G XP_011530040.1
XM_011531739.1 1282 Missense Mutation AGC,GGC S238G XP_011530041.1
XM_017007882.1 1282 Missense Mutation AGC,GGC S330G XP_016863371.1

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