Product Details

SNP ID
rs181081681
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:81811122 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGTGCCAGATGGATGGCGAGGAGAT[G/T]GAGGTCCAGGTCAGTGGGCGGCAGG
Phenotype
MIM: 138033
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
GCGR PubMed Links

Gene Details

Gene
GCGR
Gene Name
glucagon receptor
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000160.4 679 Missense Mutation ATG,ATT M128I NP_000151.1
XM_006722277.1 679 Missense Mutation ATG,ATT M128I XP_006722340.1
XM_011523539.1 679 Missense Mutation ATG,ATT M95I XP_011521841.1
XM_017024446.1 679 Missense Mutation ATG,ATT M126I XP_016879935.1
XM_017024447.1 679 Missense Mutation ATG,ATT M6I XP_016879936.1

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