Product Details

SNP ID
rs763361
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.18:69864406 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TCCATGGATTGATTGGTAGGTTGAC[C/T]GGTAGAGATGGGACTTCTATAGTTA
Phenotype
MIM: 605397
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CD226 PubMed Links

Gene Details

Gene
CD226
Gene Name
CD226 molecule
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001303618.1 561 Missense Mutation NP_001290547.1
NM_001303619.1 561 Missense Mutation NP_001290548.1
NM_006566.3 561 Missense Mutation NP_006557.2
XM_005266642.3 561 Missense Mutation XP_005266699.1
XM_005266643.3 561 Missense Mutation XP_005266700.1
XM_006722374.3 561 Missense Mutation XP_006722437.1
XM_017025524.1 561 Missense Mutation XP_016881013.1
XM_017025525.1 561 Missense Mutation XP_016881014.1
XM_017025526.1 561 Missense Mutation XP_016881015.1
XM_017025527.1 561 Missense Mutation XP_016881016.1

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