Product Details

SNP ID

rs2293998

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:132868446 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACACTGGACAATCTGACCAAGTGAA[A/C]CCCAATCCATGCTTCATCCTCCCAC

Phenotype

MIM: 188450

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

TG PubMed Links

Additional Information

For this assay, SNP(s) [rs77300255] 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

TG

Gene Name

thyroglobulin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003235.4		Intron			NP_003226.4
XM_005251038.4		Intron			XP_005251095.1
XM_005251040.4		Intron			XP_005251097.1
XM_005251042.4		Intron			XP_005251099.1
XM_006716622.3		Intron			XP_006716685.1
XM_017013793.1		Intron			XP_016869282.1
XM_017013794.1		Intron			XP_016869283.1
XM_017013795.1		Intron			XP_016869284.1
XM_017013796.1		Intron			XP_016869285.1
XM_017013797.1		Intron			XP_016869286.1
XM_017013798.1		Intron			XP_016869287.1
XM_017013799.1		Intron			XP_016869288.1
XM_017013800.1		Intron			XP_016869289.1

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