Product Details

SNP ID

rs111308948

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:188139856 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCAGGGCAGCTACGGGAGGATGCCC[A/G]CCACTGCCAAGGCGCTCTCCGATGA

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

TRIML1 PubMed Links

Additional Information

For this assay, SNP(s) [rs13131525] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

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	413	Missense Mutation	ACC,GCC	T100A	NP_848651.2
XM_006714207.3	413	Missense Mutation	ACC,GCC	T100A	XP_006714270.1
XM_011531919.1	413	Missense Mutation	ACC,GCC	T3A	XP_011530221.1

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