Product Details

SNP ID
rs186261082
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:73127365 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAAGCCGATAAAAAGTCAATTCCAC[A/T]TAACTGAATGGCTGCTAACTAAATA
Phenotype
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
C16orf47 PubMed Links

Gene Details

Gene
C16orf47
Gene Name
chromosome 16 open reading frame 47
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_207385.1 2262 Missense Mutation AAG,ATG K131M NP_997268.1
XM_017023228.1 2262 Missense Mutation AAG,ATG K131M XP_016878717.1
XM_017023229.1 2262 Missense Mutation AAG,ATG K131M XP_016878718.1

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