Product Details

SNP ID: rs3767609
Assay Type: Functionally Tested
NCBI dbSNP Submissions: 27
Location: Chr.1:111414895 on Build GRCh38
Set Membership: HapMap JSNP
Context Sequence [VIC/FAM]: CCTCCAGGGCTCACAGACTGATGAC[T/C]CACAGGGGTCACAGACTGATGACCC
Phenotype: MIM: 603578
Polymorphism: T/C, Transition Substitution
Allele Nomenclature
Literature Links: OVGP1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002557.3	1662	Missense Mutation	AGT,GGT	S536G	NP_002548.3