Product Details

SNP ID
rs141361666
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.15:72163291 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCACAAAGAAGACCTTGAGGAGCC[A/G]GTAATCCCAGAGCCTCAGCTCCCCA
Phenotype
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
GRAMD2 PubMed Links

Gene Details

Gene
GRAMD2
Gene Name
GRAM domain containing 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001012642.2 1139 Missense Mutation CGG,TGG R311W NP_001012660.1
XM_011521327.2 1139 Missense Mutation CGG,TGG R310W XP_011519629.1
XM_011521328.2 1139 Missense Mutation CGG,TGG R309W XP_011519630.1
XM_011521329.2 1139 Missense Mutation CGG,TGG R301W XP_011519631.1
XM_011521330.2 1139 Missense Mutation CGG,TGG R299W XP_011519632.1
XM_011521331.2 1139 Missense Mutation CGG,TGG R292W XP_011519633.1
XM_011521332.2 1139 Missense Mutation CGG,TGG R275W XP_011519634.1
XM_011521333.2 1139 Missense Mutation CGG,TGG R275W XP_011519635.1
XM_017021997.1 1139 Missense Mutation CGG,TGG R273W XP_016877486.1
XM_017021998.1 1139 Missense Mutation CGG,TGG R273W XP_016877487.1

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