Product Details

SNP ID

rs12302426

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:72096124 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTGATTCCTTAAGATAAATCTTTT[C/G]TTATGTGTATACACACACACACACA

Phenotype

MIM: 606950

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

TRHDE PubMed Links

Additional Information

For this assay, SNP(s) [rs144560604] 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

TRHDE

Gene Name

thyrotropin releasing hormone degrading enzyme

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_013381.2		Intron			NP_037513.1
XM_005268819.4		Intron			XP_005268876.1
XM_011538248.2		Intron			XP_011536550.1
XM_017019243.1		Intron			XP_016874732.1
XM_017019244.1		Intron			XP_016874733.1

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