Product Details

SNP ID
rs12605081
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.18:12999965 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CATAAGGTTATAGGAGTACCTCTTG[A/G]CATCAAGGGGAGGAGTGCAGAGCTT
Phenotype
MIM: 616426
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CEP192 PubMed Links

Gene Details

Gene
CEP192
Gene Name
centrosomal protein 192
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_032142.3 Intron NP_115518.3
XM_005258107.3 Intron XP_005258164.1
XM_005258109.3 Intron XP_005258166.1
XM_005258110.1 Intron XP_005258167.1
XM_006722326.3 Intron XP_006722389.1
XM_006722327.3 Intron XP_006722390.1
XM_006722330.3 Intron XP_006722393.1
XM_011525673.2 Intron XP_011523975.1
XM_011525675.2 Intron XP_011523977.1
XM_017025803.1 Intron XP_016881292.1
XM_017025804.1 Intron XP_016881293.1
XM_017025805.1 Intron XP_016881294.1
XM_017025806.1 Intron XP_016881295.1
XM_017025807.1 Intron XP_016881296.1

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