Product Details

SNP ID
rs141892594
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:101728877 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATAGCTGCACAGCTCTACAGCATCT[C/T]GATTTATCAGACAATAATATATCCC
Phenotype
MIM: 615864
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CEP97 PubMed Links

Gene Details

Gene
CEP97
Gene Name
centrosomal protein 97
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001303401.1 471 Silent Mutation CTC,CTT L129L NP_001290330.1
NM_024548.3 471 Silent Mutation CTC,CTT L129L NP_078824.2
XM_006713743.3 471 Intron XP_006713806.1
XM_011513127.1 471 Silent Mutation CTC,CTT L13L XP_011511429.1
XM_017007178.1 471 Intron XP_016862667.1

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