Product Details

SNP ID
rs199870805
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:109424057 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCAGCCCCGGGACTCTCCCTTCTGC[C/G]CCCCTTCCAACGCCTCGTCGTTGTC
Phenotype
Polymorphism
C/G, 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_207645.3 931 Missense Mutation CCC,GCC P142A NP_997528.2
XM_011542817.2 931 Missense Mutation CCC,GCC P289A XP_011541119.1
XM_011542818.2 931 Missense Mutation CCC,GCC P142A XP_011541120.1

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