Product Details

SNP ID
rs55784741
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.4:65324117 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAGAAGCGACATTTACATGAAGTTA[C/T]AATGGCACCATTCCGTTTACCAGCT
Phenotype
MIM: 600004
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
EPHA5 PubMed Links

Gene Details

Gene
EPHA5
Gene Name
EPH receptor A5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001281765.2 3652 Silent Mutation TTA,TTG L1038L NP_001268694.1
NM_001281766.2 3652 Silent Mutation TTA,TTG L1016L NP_001268695.1
NM_001281767.2 3652 Intron NP_001268696.1
NM_001318761.1 3652 Silent Mutation TTA,TTG L969L NP_001305690.1
NM_004439.7 3652 Silent Mutation TTA,TTG L1037L NP_004430.4
NM_182472.4 3652 Silent Mutation TTA,TTG L1015L NP_872272.2
XM_005265653.3 3652 Silent Mutation TTA,TTG L874L XP_005265710.1
XM_011531735.2 3652 Silent Mutation TTA,TTG L926L XP_011530037.1
XM_017007878.1 3652 Silent Mutation TTA,TTG L904L XP_016863367.1
XM_017007879.1 3652 Intron XP_016863368.1
XM_017007880.1 3652 Silent Mutation TTA,TTG L852L XP_016863369.1
XM_017007881.1 3652 Intron XP_016863370.1

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