Product Details

SNP ID
rs1469857
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.18:69861778 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AGAGTCCCAAAACTATCACGAATTA[A/G]GAATGATGTTAAAAAGATGACAATG
Phenotype
MIM: 605397
Polymorphism
A/G, 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 3189 Intron NP_001290547.1
NM_001303619.1 3189 Intron NP_001290548.1
NM_006566.3 3189 Intron NP_006557.2
XM_005266642.3 3189 UTR 3 XP_005266699.1
XM_005266643.3 3189 UTR 3 XP_005266700.1
XM_006722374.3 3189 UTR 3 XP_006722437.1
XM_017025524.1 3189 UTR 3 XP_016881013.1
XM_017025525.1 3189 UTR 3 XP_016881014.1
XM_017025526.1 3189 UTR 3 XP_016881015.1
XM_017025527.1 3189 UTR 3 XP_016881016.1

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