Product Details

SNP ID

rs4242099

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:43449486 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCAAGAAAACGAAAAATAAAAATGC[A/G]AATCTATTAAAAGAGCCCATCTGAA

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

TMEM267 PubMed Links

Additional Information

For this assay, SNP(s) [rs117224037] 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

TMEM267

Gene Name

transmembrane protein 267

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_022483.4		Intron			NP_071928.2
XM_005248333.4		Intron			XP_005248390.1
XM_005248335.3		Intron			XP_005248392.1
XM_006714486.3		Intron			XP_006714549.1
XM_011514074.2		Intron			XP_011512376.1
XM_011514075.2		Intron			XP_011512377.1

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