Product Details

SNP ID: rs2615487
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.4:87609311 on Build GRCh38
Set Membership: HapMap Validated
Context Sequence [VIC/FAM]: AACTGTAGCTCAGAAACTGGACACG[C/T]ATCACTCTGGCCTTGGCTGCAGGTA
Phenotype: MIM: 125485
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: DSPP PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014208.3		Intron			NP_055023.2