Product Details

SNP ID

rs1378879

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.11:87041924 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TTTATACTTCTAGGTTGTCAAGTCA[A/G]ATTGTTGCAGTTGCCATTATTGCTA

Phenotype

MIM: 616360

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

TMEM135 PubMed Links

Additional Information

For this assay, SNP(s) [rs78724988] 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

TMEM135

Gene Name

transmembrane protein 135

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001168724.1		Intron			NP_001162195.1
NM_022918.3		Intron			NP_075069.3
XM_017018140.1		Intron			XP_016873629.1
XM_017018141.1		Intron			XP_016873630.1
XM_017018142.1		Intron			XP_016873631.1

View Full Product Details