Product Details

SNP ID

rs9261466

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:30136063 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGAAAGCATGAGTCTTTCCACCCCC[C/T]GCCCTGAGATTTACTGACATATGAA

Phenotype

MIM: 616976

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

TRIM40 PubMed Links

Additional Information

For this assay, SNP(s) [rs190348808] 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

TRIM40

Gene Name

tripartite motif containing 40

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001286633.1	66	Intron			NP_001273562.1
NM_138700.4	66	Intron			NP_619645.1
XM_011514305.1	66	UTR 5			XP_011512607.1
XM_011514306.1	66	UTR 5			XP_011512608.1
XM_011514308.1	66	UTR 5			XP_011512610.1
XM_011514309.1	66	UTR 5			XP_011512611.1

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