Product Details

SNP ID: rs3763406
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:158732072 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CACTTCCTCTGGGCTTTGTACCTTT[A/G]ATTGTGTCTACTCTGCCTAAGTGCT
Phenotype: MIM: 616691
Polymorphism: A/G, 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	4883	UTR 3			NP_065779.1