Product Details

SNP ID
rs1055692
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:93241744 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCACTGAAAATACCTGTTCTTTTGT[G/T]ATGCTCTGCAAGTAAAATAGAAAAA
Phenotype
MIM: 602190
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
EPHA7 PubMed Links

Gene Details

Gene
EPHA7
Gene Name
EPH receptor A7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001288629.1 4920 UTR 3 NP_001275558.1
NM_001288630.1 4920 Intron NP_001275559.1
NM_004440.3 4920 UTR 3 NP_004431.1
XM_005248669.2 4920 UTR 3 XP_005248726.1
XM_005248671.2 4920 Intron XP_005248728.1
XM_017010365.1 4920 UTR 3 XP_016865854.1
XM_017010366.1 4920 Intron XP_016865855.1

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