Product Details

SNP ID
rs11260721
Assay Type
Functionally tested
NCBI dbSNP Submissions
50
Location
Chr.1:16128557 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ACCTCCCAGCCTCCCGGTCTGTTCC[C/T]GCCATGATCTTTGACCATGCACAAG
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 Intron XP_016856023.1
XM_017000535.1 Intron XP_016856024.1
XM_017000536.1 Intron XP_016856025.1
XM_017000537.1 Intron XP_016856026.1

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