Product Details

SNP ID: rs999332
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.18:74316093 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TGCAGGAGGCCGTGGGCGTTAGAAG[C/T]GTTGCTTTTCCAGTTTGTAAGACCA
Phenotype
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: C18orf63 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001174123.1	219	UTR 5			NP_001167594.1