Product Details

SNP ID: rs116134185
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:158733095 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGGCTGCTGAGAACAGCAGGGGCCG[A/G]GCTCGCAGCTGTGGCGCCCCCAACC
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	3860	UTR 3			NP_065779.1