Product Details

SNP ID

rs75033823

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:65637177 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTGAAGGATGGAAGCTCTCTTTTG[A/C]AGAAAATTAACCTAGAAAAGACACC

Phenotype

Polymorphism

A/C, Transversion 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	3061	Silent Mutation	CTG,CTT	L193L	NP_001032402.1
NM_001199165.2	3061	Silent Mutation	CTG,CTT	L937L	NP_001186094.1
NM_001302891.1	3061	Silent Mutation	CTG,CTT	L895L	NP_001289820.1
XM_005257119.4	3061	Silent Mutation	CTG,CTT	L938L	XP_005257176.1
XM_005257125.3	3061	Silent Mutation	CTG,CTT	L630L	XP_005257182.1
XM_005257126.4	3061	Silent Mutation	CTG,CTT	L529L	XP_005257183.1
XM_006721740.2	3061	Silent Mutation	CTG,CTT	L938L	XP_006721803.1
XM_006721744.3	3061	Intron			XP_006721807.1
XM_011524461.2	3061	Silent Mutation	CTG,CTT	L937L	XP_011522763.1
XM_011524462.2	3061	Intron			XP_011522764.1
XM_011524463.2	3061	Intron			XP_011522765.1
XM_011524464.2	3061	Silent Mutation	CTG,CTT	L867L	XP_011522766.1
XM_011524465.2	3061	Silent Mutation	CTG,CTT	L707L	XP_011522767.1
XM_011524466.2	3061	Silent Mutation	CTG,CTT	L585L	XP_011522768.1
XM_011524467.2	3061	Silent Mutation	CTG,CTT	L532L	XP_011522769.1
XM_017024302.1	3061	Silent Mutation	CTG,CTT	L895L	XP_016879791.1
XM_017024303.1	3061	Intron			XP_016879792.1

View Full Product Details