Product Details

SNP ID

rs9261536

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:30163572 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCTCTCTTTCTCTCTCTCTGTCTCT[C/T]AGCCTTGCAGCCGTTTCCCTCTGCG

Phenotype

MIM: 605701

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

TRIM10 PubMed Links

Additional Information

For this assay, SNP(s) [rs546780690] 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

TRIM10

Gene Name

tripartite motif containing 10

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006778.3	367	Intron			NP_006769.2
NM_052828.2	367	Intron			NP_439893.2
XM_011514221.1	367	Intron			XP_011512523.1
XM_011514222.2	367	Intron			XP_011512524.1
XM_011514223.2	367	Intron			XP_011512525.1
XM_011514225.1	367	Intron			XP_011512527.1

Gene

TRIM15

Gene Name

tripartite motif containing 15

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_033229.2	367	UTR 5			NP_150232.2
XM_011514987.1	367	UTR 5			XP_011513289.1
XM_011514988.2	367	Intron			XP_011513290.1

View Full Product Details