Product Details

SNP ID
rs201833020
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:101726667 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATTTACCCTGTGAAGCTGATATTCA[C/G]ACTTTGATTCTGGATAAAAATCAGA
Phenotype
MIM: 615864
Polymorphism
C/G, Transversion 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_001303401.1 201 Silent Mutation CAC,CAG H39Q NP_001290330.1
NM_024548.3 201 Silent Mutation CAC,CAG H39Q NP_078824.2
XM_006713743.3 201 Missense Mutation CAC,CAG H39Q XP_006713806.1
XM_011513127.1 201 UTR 5 XP_011511429.1
XM_017007178.1 201 Missense Mutation CAC,CAG H39Q XP_016862667.1

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