Product Details

SNP ID: rs16888382
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.8:39939897 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CTTTTAGGAAACAAGTAAATGAGGT[C/T]CTAAAAAGTTAAACTGTGACCATAT
Phenotype: MIM: 612129
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: IDO2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_194294.2		Intron			NP_919270.2