Product Details

SNP ID
rs1803527
Assay Type
Functionally tested
NCBI dbSNP Submissions
62
Location
Chr.1:16124918 on Build GRCh38
Set Membership
HapMap JSNP
Context Sequence [VIC/FAM]
AGGGAAGGTCGGCTTGGGAATATCC[C/T]ATATGTCTGTCCGAAGGCTGTGGCG
Phenotype
MIM: 176946
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
EPHA2 PubMed Links

Gene Details

Gene
EPHA2
Gene Name
EPH receptor A2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
XM_017000534.1 3306 UTR 3 XP_016856023.1
XM_017000535.1 3306 UTR 3 XP_016856024.1
XM_017000536.1 3306 UTR 3 XP_016856025.1
XM_017000537.1 3306 Intron XP_016856026.1

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