Product Details

SNP ID
rs148816646
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:109423689 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGGCGTTGCCGCCGTGTCTCCTCA[A/C]CCGGACCTTTGCTTCCCCCAACGCC
Phenotype
Polymorphism
A/C, 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_207645.3 563 Missense Mutation AAC,ACC N19T NP_997528.2
XM_011542817.2 563 Missense Mutation AAC,ACC N166T XP_011541119.1
XM_011542818.2 563 Missense Mutation AAC,ACC N19T XP_011541120.1

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