Product Details

SNP ID: rs146901313
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.X:115009546 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CACCAAGGTAGTATCATCTTCTCTG[A/G]TCTCAATTTCATAATCAAAACACCT
Phenotype: MIM: 300130
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: IL13RA2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000640.2	952	Missense Mutation	ACC,ATC	T276I	NP_000631.1