Product Details

SNP ID: rs200244502
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.8:39918203 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGGGGCAAAGGTCATGGAGATGTCC[A/G]TAAGGTTTGGAGATTTTCTCAGATT
Phenotype: MIM: 147435
Polymorphism: A/G, 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	413	Missense Mutation	CAT,CGT	H100R	NP_002155.1