Product Details

SNP ID: rs28917214
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:151744932 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GGTTGGAGGTTTTAGCCCCATTTTA[A/C]CGATGGGAAGACCAAATCTCTGTAA
Phenotype: MIM: 602270
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: ATOX1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004045.3		Intron			NP_004036.1