Product Details

SNP ID: rs3763412
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:158732395 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GTATTTGTCTATAAAGGTATTGATA[C/T]GCTTCCCAAATAATCCTATATACTA
Phenotype: MIM: 616691
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: ESYT2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020728.2	4560	UTR 3			NP_065779.1