Product Details

SNP ID: rs144479719
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:66315167 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGGTTAGTGGGGCTCTGAGAGGGCA[A/G]GAGGGTGGGGAGGGCTGCGGGCTGG
Phenotype: MIM: 606064
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: CD248 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020404.2	1878	Silent Mutation	CTG,TTG	L621L	NP_065137.1