Product Details

SNP ID: rs2233384
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.2:233032704 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CCCTTCCTGTCCTGCAGAAGGAGAG[A/C]GTGTTCCAGTCGGGAGCCCATGCCT
Phenotype: MIM: 605528
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: NEU2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005383.2	33	Missense Mutation	AGA,AGC	R11S	NP_005374.2