Product Details

SNP ID
rs111912421
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:101726726 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGGAAAATCTGGAGAAATGCAAAC[A/G]ATTAATACAGGTAGGTATTGCAATC
Phenotype
MIM: 615864
Polymorphism
A/G, 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_001303401.1 260 Missense Mutation CAA,CGA Q59R NP_001290330.1
NM_024548.3 260 Missense Mutation CAA,CGA Q59R NP_078824.2
XM_006713743.3 260 Missense Mutation CAA,CGA Q59R XP_006713806.1
XM_011513127.1 260 UTR 5 XP_011511429.1
XM_017007178.1 260 Missense Mutation CAA,CGA Q59R XP_016862667.1

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