Product Details

SNP ID
rs201110271
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:89107797 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTCCTTCTCAGCTGCTCTGTTCTC[C/G]ACAGCTTCGGGGAACTGATTCCGCA
Phenotype
MIM: 179611
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
EPHA3 PubMed Links

Gene Details

Gene
EPHA3
Gene Name
EPH receptor A3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_005233.5 199 Missense Mutation CAC,GAC H17D NP_005224.2
NM_182644.2 199 Missense Mutation CAC,GAC H17D NP_872585.1
XM_005264715.2 199 Missense Mutation CAC,GAC H17D XP_005264772.1
XM_005264716.2 199 Missense Mutation CAC,GAC H17D XP_005264773.1

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