Product Details

SNP ID
rs112281664
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.4:188139767 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCCCGCATTTCCAGTCAAACGAGC[A/G]TCTGGGGAGGCTGGCCAGCATCGCC
Phenotype
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
TRIML1 PubMed Links

Gene Details

Gene
TRIML1
Gene Name
tripartite motif family like 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_178556.3 324 Missense Mutation CAT,CGT H70R NP_848651.2
XM_006714207.3 324 Missense Mutation CAT,CGT H70R XP_006714270.1
XM_011531919.1 324 UTR 5 XP_011530221.1

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