Product Details

SNP ID

rs3109904

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:58812942 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCACTACTCAACAATTATTTTGACT[A/C]CTTACCATGATCAAGGCATTGTTAA

Phenotype

MIM: 606863

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

TOX PubMed Links

Gene Details

Gene

TOX

Gene Name

thymocyte selection associated high mobility group box

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014729.2		Intron			NP_055544.1
XM_017014085.1		Intron			XP_016869574.1

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