Product Details

SNP ID
rs73323492
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:93501797 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTAACAACATACATTGAGGTAAATG[C/T]TTTTTCAAGCACTTAGAGAACAGTC
Phenotype
MIM: 610000
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CEP55 PubMed Links

Gene Details

Gene
CEP55
Gene Name
centrosomal protein 55
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001127182.1 Intron NP_001120654.1
NM_018131.4 Intron NP_060601.3
XM_011539918.1 Intron XP_011538220.1
XM_011539919.1 Intron XP_011538221.1
XM_011539920.2 Intron XP_011538222.1
XM_017016372.1 Intron XP_016871861.1
XM_017016373.1 Intron XP_016871862.1

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