Product Details

SNP ID
rs142035564
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:57696337 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGACCTATGGCAATGGGTCCAAGTG[C/T]GACCTTAATGGGAGGCCCCGGGAGG
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_001017956.2 682 Silent Mutation TGC,TGT C181C NP_001017956.1
NM_001017957.2 682 Silent Mutation TGC,TGT C181C NP_001017957.1
NM_001017958.2 682 Silent Mutation TGC,TGT C181C NP_001017958.1
NM_001261420.1 682 Silent Mutation TGC,TGT C181C NP_001248349.1
NM_001261421.1 682 Intron NP_001248350.1
NM_001261422.1 682 Intron NP_001248351.1
NM_001261423.1 682 Silent Mutation TGC,TGT C122C NP_001248352.1
NM_006812.3 682 Silent Mutation TGC,TGT C181C NP_006803.1
XM_005268581.1 682 Silent Mutation TGC,TGT C181C XP_005268638.1
XM_006719200.1 682 Silent Mutation TGC,TGT C181C XP_006719263.1
XM_006719201.1 682 Silent Mutation TGC,TGT C181C XP_006719264.1

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