Product Details

SNP ID

rs142765947

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:65637141 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCTGTACCTTCTGCCTTGATATGT[A/C]GTCAGTTCTTCCTGAAGGATGGAAG

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	3097	Silent Mutation	ACG,ACT	T205T	NP_001032402.1
NM_001199165.2	3097	Silent Mutation	ACG,ACT	T949T	NP_001186094.1
NM_001302891.1	3097	Silent Mutation	ACG,ACT	T907T	NP_001289820.1
XM_005257119.4	3097	Silent Mutation	ACG,ACT	T950T	XP_005257176.1
XM_005257125.3	3097	Silent Mutation	ACG,ACT	T642T	XP_005257182.1
XM_005257126.4	3097	Silent Mutation	ACG,ACT	T541T	XP_005257183.1
XM_006721740.2	3097	Silent Mutation	ACG,ACT	T950T	XP_006721803.1
XM_006721744.3	3097	Intron			XP_006721807.1
XM_011524461.2	3097	Silent Mutation	ACG,ACT	T949T	XP_011522763.1
XM_011524462.2	3097	Intron			XP_011522764.1
XM_011524463.2	3097	Intron			XP_011522765.1
XM_011524464.2	3097	Silent Mutation	ACG,ACT	T879T	XP_011522766.1
XM_011524465.2	3097	Silent Mutation	ACG,ACT	T719T	XP_011522767.1
XM_011524466.2	3097	Silent Mutation	ACG,ACT	T597T	XP_011522768.1
XM_011524467.2	3097	Silent Mutation	ACG,ACT	T544T	XP_011522769.1
XM_017024302.1	3097	Silent Mutation	ACG,ACT	T907T	XP_016879791.1
XM_017024303.1	3097	Intron			XP_016879792.1

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