Product Details

SNP ID

rs145069838

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:188091535 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAATGAGGGACATCTCGGTCACATT[A/G]TAGAATGATATCTGCCCGTGTTCGC

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

TRIML2 PubMed Links

Additional Information

For this assay, SNP(s) [rs17881718] are located under a probe 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	1446	Silent Mutation	TAC,TAT	Y409Y	NP_001290348.1
NM_173553.2	1446	UTR 3			NP_775824.2
XM_011531737.2	1446	Silent Mutation	TAC,TAT	Y384Y	XP_011530039.1
XM_011531738.1	1446	Silent Mutation	TAC,TAT	Y384Y	XP_011530040.1
XM_011531739.1	1446	Silent Mutation	TAC,TAT	Y292Y	XP_011530041.1
XM_017007882.1	1446	Silent Mutation	TAC,TAT	Y384Y	XP_016863371.1

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