Product Details

SNP ID: rs917864
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.22:17085042 on Build GRCh38
Set Membership: HapMap Validated
Context Sequence [VIC/FAM]: GGAAAAGAAAGCCTCAGAACGTTCG[C/T]TCGCTGCGTCCCCAGCCGGGGCCGA
Phenotype: MIM: 605461
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: IL17RA PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001289905.1	84	UTR 5			NP_001276834.1
NM_014339.6	84	UTR 5			NP_055154.3