Product Details

SNP ID: rs138012316
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.10:122698026 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AAAACTACATTCATTTTTATTTCTC[G/T]TCTTTTTGTGTTTTTTCCCTCTGCC
Phenotype
Polymorphism: G/T, Transversion substitution
Allele Nomenclature
Literature Links: C10orf120 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001010912.2	747	Silent Mutation			NP_001010912.1