Product Details

SNP ID: rs12462533
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.19:51105298 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GGGTGAGAAAATGGGTGGGCCTCCA[A/C]GATTGAACTCAACCCTGCTCTGGTA
Phenotype: MIM: 612694
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: CTU1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_145232.3		Intron			NP_660275.2