Product Details

SNP ID

rs41313993

Assay Type

Functionally Tested

NCBI dbSNP Submissions

13

Location

Chr.1:114397011 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAAGTTGATTAAATGATAACTAGTG[A/G]TAGTGTTTCCTAAACCCTAAGTATG

Phenotype

MIM: 605769

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

TRIM33 PubMed Links

Additional Information

For this assay, SNP(s) [rs144710406] 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

TRIM33

Gene Name

tripartite motif containing 33

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015906.3	3380	UTR 3			NP_056990.3
NM_033020.2	3380	UTR 3			NP_148980.2
XM_005270936.3	3380	UTR 3			XP_005270993.1
XM_005270937.3	3380	UTR 3			XP_005270994.1
XM_011541568.2	3380	UTR 3			XP_011539870.1
XM_017001452.1	3380	UTR 3			XP_016856941.1
XM_017001453.1	3380	UTR 3			XP_016856942.1
XM_017001454.1	3380	Intron			XP_016856943.1

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