Product Details

SNP ID
rs138186337
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:57694764 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTCTTTCCCAGAGCCAATCTTCGGA[C/T]GTGGTGATTGTCTCCTCTAAGTACA
Phenotype
MIM: 609677
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
OS9 PubMed Links

Gene Details

Gene
OS9
Gene Name
OS9, endoplasmic reticulum lectin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001017956.2 316 Silent Mutation GAC,GAT D59D NP_001017956.1
NM_001017957.2 316 Silent Mutation GAC,GAT D59D NP_001017957.1
NM_001017958.2 316 Silent Mutation GAC,GAT D59D NP_001017958.1
NM_001261420.1 316 Silent Mutation GAC,GAT D59D NP_001248349.1
NM_001261421.1 316 Silent Mutation GAC,GAT D59D NP_001248350.1
NM_001261422.1 316 Silent Mutation GAC,GAT D59D NP_001248351.1
NM_001261423.1 316 Intron NP_001248352.1
NM_006812.3 316 Silent Mutation GAC,GAT D59D NP_006803.1
XM_005268581.1 316 Silent Mutation GAC,GAT D59D XP_005268638.1
XM_006719200.1 316 Silent Mutation GAC,GAT D59D XP_006719263.1
XM_006719201.1 316 Silent Mutation GAC,GAT D59D XP_006719264.1

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