Product Details

SNP ID: rs2947594
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.10:122697936 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GCGATGGACCGTTCCGGTTTCTTTG[C/T]GGGGAGGAATGATTTGCGATCATTT
Phenotype
Polymorphism: C/T, Transition 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	837	Missense Mutation	ACA,GCA	T269A	NP_001010912.1