Product Details

SNP ID
rs1059048
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:65635680 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AATTCTATGCAAAAGGATTAACAAG[A/G]CATATCATAGGAAATCACTTTGCCC
Phenotype
Polymorphism
A/G, 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 3409 UTR 3 NP_001032402.1
NM_001199165.2 3409 UTR 3 NP_001186094.1
NM_001302891.1 3409 UTR 3 NP_001289820.1
XM_005257119.4 3409 UTR 3 XP_005257176.1
XM_005257125.3 3409 UTR 3 XP_005257182.1
XM_005257126.4 3409 UTR 3 XP_005257183.1
XM_006721740.2 3409 UTR 3 XP_006721803.1
XM_006721744.3 3409 Intron XP_006721807.1
XM_011524461.2 3409 UTR 3 XP_011522763.1
XM_011524462.2 3409 Intron XP_011522764.1
XM_011524463.2 3409 Intron XP_011522765.1
XM_011524464.2 3409 UTR 3 XP_011522766.1
XM_011524465.2 3409 UTR 3 XP_011522767.1
XM_011524466.2 3409 UTR 3 XP_011522768.1
XM_011524467.2 3409 UTR 3 XP_011522769.1
XM_017024302.1 3409 UTR 3 XP_016879791.1
XM_017024303.1 3409 Intron XP_016879792.1

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