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SNP ID

rs557782633

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:184567302 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCAGGGCTGGGGCTGTTTCCCTACA[C/T]CTCTGGCTAAGGCTGCCCCAGCACC

Phenotype

MIM: 601839

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

EPHB3 PubMed Links

Gene Details

Gene

EPHB3

Gene Name

EPH receptor B3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004443.3		Intron			NP_004434.2

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