Product Details

SNP ID
rs200416866
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.20:34850032 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCGGGCCAGGCTGTCACTCAGGTTC[C/T]GGTTCAAGGTCAGGACATTCAGCAG
Phenotype
MIM: 612342
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
GGT7 PubMed Links

Gene Details

Gene
GGT7
Gene Name
gamma-glutamyltransferase 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_178026.2 1276 Missense Mutation CAG,CGG Q585R NP_821158.2
XM_011528782.2 1276 Missense Mutation CAG,CGG Q351R XP_011527084.1
XM_011528783.2 1276 Missense Mutation CAG,CGG Q302R XP_011527085.1
XM_017027809.1 1276 Missense Mutation CAG,CGG Q585R XP_016883298.1
XM_017027810.1 1276 UTR 3 XP_016883299.1
XM_017027811.1 1276 Intron XP_016883300.1

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