Product Details

SNP ID: rs12506827
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:4191846 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: ATCTTGGTCATTGCTGTACCCTCAA[A/C]ATGCATAGCAGTCCCTGAACCTCTG
Phenotype: MIM: 607806
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: OTOP1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_177998.1		Intron			NP_819056.1