Product Details

SNP ID: rs11871637
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:61412874 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CCGCGGGGCTGGGCCCTCGCGTTCT[C/T]TCTGCGGGAAGTGAGCCGCCGGCCT
Phenotype: MIM: 600747
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: C17orf82 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_203425.2	1124	UTR 3			NP_982249.2

There are no transcripts associated with this gene.