Product Details

SNP ID: rs9916859
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:34574442 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GCAGTTGGGCAAAAACCTGAATGAA[A/G]TAAAGGAGCAAGGGGTTAGGGGAAA
Phenotype: MIM: 616178
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: C17orf102 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_207454.2	3678	UTR 3			NP_997337.2

There are no transcripts associated with this gene.