Product Details

SNP ID
rs10513982
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.18:69860560 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GCATTGCAGTTAATTCTAGAAGCTA[C/T]TTTTCTACCTATTGAATCACTAGAA
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 4407 Intron NP_001290547.1
NM_001303619.1 4407 Intron NP_001290548.1
NM_006566.3 4407 Intron NP_006557.2
XM_005266642.3 4407 UTR 3 XP_005266699.1
XM_005266643.3 4407 UTR 3 XP_005266700.1
XM_006722374.3 4407 UTR 3 XP_006722437.1
XM_017025524.1 4407 UTR 3 XP_016881013.1
XM_017025525.1 4407 UTR 3 XP_016881014.1
XM_017025526.1 4407 UTR 3 XP_016881015.1
XM_017025527.1 4407 UTR 3 XP_016881016.1

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