Product Details

SNP ID

rs1802658

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:15621370 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCCACTCCTGAATCACTAGCGGCAG[A/C]ACTGATTTTTTCCTGTCGTCTTCTC

Phenotype

MIM: 600206

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

EPS8 PubMed Links

Gene Details

Gene

EPS8

Gene Name

epidermal growth factor receptor pathway substrate 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004447.5	2913	Missense Mutation			NP_004438.3
XM_011520605.2	2913	Missense Mutation			XP_011518907.1

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