Product Details

SNP ID: rs11995570
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.8:39921211 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: AAGATTAATTTTTTTTTTTAAAGAT[C/T]GCTGGGAAAAGTGGGTGAATCACCT
Phenotype: MIM: 147435
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: IDO1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002164.5		Intron			NP_002155.1