Product Details

SNP ID
rs7626103
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:68979040 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTATTTAAATACAGAGTCAAATCA[C/T]TTTTAAAATGAAACCATAGAACCCA
Phenotype
MIM: 614789
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
EOGT PubMed Links

Gene Details

Gene
EOGT
Gene Name
EGF domain specific O-linked N-acetylglucosamine transferase
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001278689.1 Intron NP_001265618.1
NM_173654.2 Intron NP_775925.1
XM_005264743.2 Intron XP_005264800.1
XM_011533599.1 Intron XP_011531901.1
XM_011533600.1 Intron XP_011531902.1
XM_011533602.1 Intron XP_011531904.1
XM_011533603.1 Intron XP_011531905.1
XM_017006204.1 Intron XP_016861693.1
XM_017006205.1 Intron XP_016861694.1
XM_017006206.1 Intron XP_016861695.1
XM_017006207.1 Intron XP_016861696.1
XM_017006208.1 Intron XP_016861697.1
XM_017006209.1 Intron XP_016861698.1

View Full Product Details