Product Details

SNP ID
rs3177117
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:221418045 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AACCAGATTGCAGGGTTGTATACGG[C/T]AACTACTTTATTATTTTCAAATGCA
Phenotype
MIM: 602188
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
EPHA4 PubMed Links

Gene Details

Gene
EPHA4
Gene Name
EPH receptor A4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001304536.1 6398 UTR 3 NP_001291465.1
NM_001304537.1 6398 UTR 3 NP_001291466.1
NM_004438.4 6398 UTR 3 NP_004429.1
XM_005246374.2 6398 UTR 3 XP_005246431.1

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