Product Details

SNP ID
rs182452644
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:78236385 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCGTGAAGCTGCGCCGCGACAGCG[C/T]GGCGGACTTCTTCTCCCACTACGAG
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CEP78 PubMed Links

Gene Details

Gene
CEP78
Gene Name
centrosomal protein 78
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001098802.1 324 Missense Mutation GCG,GTG A12V NP_001092272.1
NM_032171.1 324 Missense Mutation GCG,GTG A12V NP_115547.1
XM_005252263.4 324 Missense Mutation GCG,GTG A12V XP_005252320.1
XM_005252265.2 324 Missense Mutation GCG,GTG A12V XP_005252322.1
XM_005252266.4 324 UTR 5 XP_005252323.1
XM_017015192.1 324 Missense Mutation GCG,GTG A12V XP_016870681.1
XM_017015193.1 324 Missense Mutation GCG,GTG A12V XP_016870682.1
XM_017015194.1 324 Missense Mutation GCG,GTG A12V XP_016870683.1
XM_017015195.1 324 Missense Mutation GCG,GTG A12V XP_016870684.1
XM_017015196.1 324 UTR 5 XP_016870685.1

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