Product Details

SNP ID
rs9916106
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:65641273 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGTGACTCTGAGAGAGATGGTCCC[C/T]GTAACAATGCTTTATTTATTTAAAA
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CEP112 PubMed Links

Gene Details

Gene
CEP112
Gene Name
centrosomal protein 112
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001037325.2 Intron NP_001032402.1
NM_001199165.2 Intron NP_001186094.1
NM_001302891.1 Intron NP_001289820.1
XM_005257119.4 Intron XP_005257176.1
XM_005257125.3 Intron XP_005257182.1
XM_005257126.4 Intron XP_005257183.1
XM_006721740.2 Intron XP_006721803.1
XM_006721744.3 Intron XP_006721807.1
XM_011524461.2 Intron XP_011522763.1
XM_011524462.2 Intron XP_011522764.1
XM_011524463.2 Intron XP_011522765.1
XM_011524464.2 Intron XP_011522766.1
XM_011524465.2 Intron XP_011522767.1
XM_011524466.2 Intron XP_011522768.1
XM_011524467.2 Intron XP_011522769.1
XM_017024302.1 Intron XP_016879791.1
XM_017024303.1 Intron XP_016879792.1

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