Product Details

SNP ID: rs2069745
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:132659067 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: ACCGCCTCCCATCTGATTTGTCTTG[C/G]TCAACAGTGGCCCAGGCCACTCCTA
Phenotype: MIM: 147683
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: IL13 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002188.2		Intron			NP_002179.2

There are no transcripts associated with this gene.