Product Details

SNP ID: rs1491991
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.3:190388764 on Build GRCh38
Set Membership: HapMap Validated
Context Sequence [VIC/FAM]: AATTCACGTCTTCCATTGCTGCATA[T/C]ATCATATTGAGTAACATTTCAGTAC
Phenotype: MIM: 603959
Polymorphism: T/C, Transition substitution
Allele Nomenclature
Literature Links: CLDN16 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006580.3		Intron			NP_006571.1