Product Details

SNP ID: rs201594392
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.2:219418705 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GGCTGGGGACCACCCGCACGCCCTC[C/T]TCCTACGGCGCAGGCGAGCTGCTGG
Phenotype: MIM: 125660
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: DES PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001927.3	329	Silent Mutation	TCC,TCT	S81S	NP_001918.3