Product Details

SNP ID
rs148139786
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:55953197 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTGGAACCCTATAAACTTGAAAAT[A/G]CAAGATTGAGTAGAGAAAATAATGA
Phenotype
MIM: 611423
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CEP135 PubMed Links

Gene Details

Gene
CEP135
Gene Name
centrosomal protein 135
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_025009.4 494 Missense Mutation ACA,GCA T76A NP_079285.2
XM_005265788.3 494 UTR 5 XP_005265845.1
XM_006714055.2 494 Missense Mutation ACA,GCA T76A XP_006714118.1
XM_011534412.2 494 Intron XP_011532714.1

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