Product Details

SNP ID: rs12121124
Assay Type: Functionally tested
NCBI dbSNP Submissions: 32
Location: Chr.1:58576329 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CGACCACCACGATGACGGCGATGAG[A/G]CCGGCGGTGAGGCGCTTCATGGAGA
Phenotype: MIM: 137290
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: TACSTD2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002353.2	1166	Silent Mutation	GGC,GGT	G276G	NP_002344.2