Product Details

SNP ID: rs148441092
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:117989506 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CCAGACCCTGTCCTATGACCTTACC[A/G]CAGTGACCTTGGACCTGTACCACAG
Phenotype: MIM: 146933
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: IL10RA PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001558.3	330	Missense Mutation	ACA,GCA	T85A	NP_001549.2