Product Details

SNP ID
rs199735397
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:93667786 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAAGTTTAAGAAGTATGGGAGAGGG[A/T]CATCGACAGGCCAAAGAAAATGTGA
Phenotype
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
CEP295 PubMed Links

Gene Details

Gene
CEP295
Gene Name
centrosomal protein 295
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_033395.1 403 Silent Mutation GGA,GGT G96G NP_203753.1
XM_005274366.1 403 Silent Mutation GGA,GGT G96G XP_005274423.1
XM_005274367.2 403 Silent Mutation GGA,GGT G96G XP_005274424.1
XM_005274368.2 403 Silent Mutation GGA,GGT G96G XP_005274425.1
XM_011543047.1 403 Silent Mutation GGA,GGT G96G XP_011541349.1
XM_011543048.1 403 Silent Mutation GGA,GGT G96G XP_011541350.1
XM_011543049.1 403 Silent Mutation GGA,GGT G96G XP_011541351.1
XM_011543050.2 403 Intron XP_011541352.1
XM_011543053.2 403 Intron XP_011541355.1
XM_011543054.2 403 Intron XP_011541356.1
XM_017018470.1 403 Silent Mutation GGA,GGT G96G XP_016873959.1
XM_017018471.1 403 Silent Mutation GGA,GGT G96G XP_016873960.1
XM_017018472.1 403 Silent Mutation GGA,GGT G96G XP_016873961.1
XM_017018473.1 403 UTR 5 XP_016873962.1
XM_017018474.1 403 Intron XP_016873963.1
XM_017018475.1 403 UTR 5 XP_016873964.1
XM_017018476.1 403 Intron XP_016873965.1

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