Product Details

SNP ID: rs199677542
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:117989520 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ATGACCTTACCGCAGTGACCTTGGA[C/T]CTGTACCACAGCAATGGCTACCGGG
Phenotype: MIM: 146933
Polymorphism: C/T, 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	344	Silent Mutation	GAC,GAT	D89D	NP_001549.2