Product Details

SNP ID

rs209736

Assay Type

Functionally tested

NCBI dbSNP Submissions

70

Location

Chr.1:22564916 on Build GRCh38

Set Membership

HapMap JSNP

Context Sequence [VIC/FAM]

TGCTGCTCTTCCACGCCCAGACAGA[C/T]CACACATCTGCCCTTCACACACAGC

Phenotype

MIM: 176945

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

EPHA8 PubMed Links

Gene Details

Gene

EPHA8

Gene Name

EPH receptor A8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_011540969.1		Intron			XP_011539271.1
XM_011540970.1		Intron			XP_011539272.1
XM_011540972.1		Intron			XP_011539274.1
XM_011540973.1		Intron			XP_011539275.1
XM_011540975.2		Intron			XP_011539277.1

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