Product Details

SNP ID
rs202022682
Assay Type
Functionally tested
NCBI dbSNP Submissions
3
Location
Chr.1:3816284 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTCAGCGGCGCTGTCCCTCACCTGG[C/T]TGCAGTGCCGGGGCCTTCTGCAGAA
Phenotype
MIM: 616690
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CEP104 PubMed Links

Gene Details

Gene
CEP104
Gene Name
centrosomal protein 104
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_014704.3 3119 Silent Mutation CAA,CAG Q886Q NP_055519.1
XM_005244815.4 3119 Silent Mutation CAA,CAG Q922Q XP_005244872.1
XM_011542473.2 3119 Silent Mutation CAA,CAG Q928Q XP_011540775.1
XM_011542474.2 3119 Silent Mutation CAA,CAG Q892Q XP_011540776.1
XM_011542475.2 3119 Silent Mutation CAA,CAG Q870Q XP_011540777.1
XM_011542476.2 3119 Silent Mutation CAA,CAG Q862Q XP_011540778.1
XM_011542477.2 3119 Silent Mutation CAA,CAG Q804Q XP_011540779.1
XM_011542478.1 3119 Intron XP_011540780.1
XM_017002917.1 3119 Silent Mutation CAA,CAG Q864Q XP_016858406.1
XM_017002918.1 3119 Silent Mutation CAA,CAG Q828Q XP_016858407.1
XM_017002919.1 3119 Silent Mutation CAA,CAG Q820Q XP_016858408.1

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