Product Details

SNP ID

rs10406927

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:14545319 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTACCCCAGGGCCTTTGCATTCCCC[A/G]CCAGGGAGCCTCATGCTGGCCCTCA

Phenotype

MIM: 610057

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

TECR PubMed Links

Additional Information

For this assay, SNP(s) [rs74852236] 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

TECR

Gene Name

trans-2,3-enoyl-CoA reductase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001321170.1		Intron			NP_001308099.1
NM_138501.5		Intron			NP_612510.1
XM_006722945.1		Intron			XP_006723008.1
XM_011528442.2		Intron			XP_011526744.1

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