Product Details

SNP ID
rs1805749
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:8992295 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTTCTGAGTGTGCTGCTATACCAG[C/T]GGATCCTGTGCCAGGGTAAGTGCAA
Phenotype
MIM: 604874
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
KLRG1 PubMed Links

Gene Details

Gene
KLRG1
Gene Name
killer cell lectin like receptor G1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_005810.3 728 Missense Mutation CGG,TGG R58W NP_005801.3
XM_017018682.1 728 Missense Mutation CGG,TGG R58W XP_016874171.1
XM_017018683.1 728 Missense Mutation CGG,TGG R58W XP_016874172.1
XM_017018684.1 728 Missense Mutation CGG,TGG R58W XP_016874173.1
XM_017018685.1 728 Missense Mutation CGG,TGG R58W XP_016874174.1

View Full Product Details