Product Details

SNP ID: rs148466782
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.21:33276637 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GATAAATGCATGAATACTACCTTGA[C/T]GGAATGTGATTTCTCAAGTCTTTCC
Phenotype: MIM: 123889
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: IL10RB PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000628.4	321	Missense Mutation	ACG,ATG	T72M	NP_000619.3