Product Details

SNP ID

rs201585762

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:188091548 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCGGTCACATTGTAGAATGATATC[G/T]GCCCGTGTTCGCAGTCAAGGAAAAC

Phenotype

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

TRIML2 PubMed Links

Additional Information

For this assay, SNP(s) [rs2279550] 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

TRIML2

Gene Name

tripartite motif family like 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001303419.1	1433	Missense Mutation			NP_001290348.1
NM_173553.2	1433	UTR 3			NP_775824.2
XM_011531737.2	1433	Missense Mutation			XP_011530039.1
XM_011531738.1	1433	Missense Mutation			XP_011530040.1
XM_011531739.1	1433	Missense Mutation			XP_011530041.1
XM_017007882.1	1433	Missense Mutation			XP_016863371.1

View Full Product Details