Product Details

SNP ID: rs201980658
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:117988399 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CTCCCCAGGGACAGAGCTGCCCAGC[C/G]CTCCGTCTGTGTGGTTTGAAGCAGA
Phenotype: MIM: 146933
Polymorphism: C/G, Transversion 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	162	Missense Mutation	CCT,GCT	P29A	NP_001549.2