Product Details

SNP ID

rs115862421

Assay Type

Functionally tested

NCBI dbSNP Submissions

12

Location

Chr.1:16129186 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCAGTAAACAGTAGCTACTGTTAT[G/T]ATTACGGTTACTATTATTTCCCCAC

Phenotype

MIM: 176946

Polymorphism

G/T, Transversion 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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