Product Details

SNP ID: rs13229349
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:158731839 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TTTTGACAACTCAAGAGTGTCTGAC[A/G]TCGCTGGGATCCTGGAGTGCTGAGT
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	5116	UTR 3			NP_065779.1