Product Details

SNP ID
rs138823718
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:109424054 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAGGCAGCCCCGGGACTCTCCCTTC[A/T]GCGCCCCTTCCAACGCCTCGTCGTT
Phenotype
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
C11orf87 PubMed Links

Gene Details

Gene
C11orf87
Gene Name
chromosome 11 open reading frame 87
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_207645.3 928 Missense Mutation AGC,TGC S141C NP_997528.2
XM_011542817.2 928 Missense Mutation AGC,TGC S288C XP_011541119.1
XM_011542818.2 928 Missense Mutation AGC,TGC S141C XP_011541120.1

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