Product Details

SNP ID
rs746842
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.10:92291231 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GCCCGCGGTCCATGGACCGGAACCT[C/G]GGGCCGACGGACGGGAACCCGGGCC
Phenotype
MIM: 610606 MIM: 610637
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
CPEB3 PubMed Links
Additional Information
For this assay, SNP(s) [rs115311029] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene
CPEB3
Gene Name
cytoplasmic polyadenylation element binding protein 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001178137.1 69 Intron NP_001171608.1
NM_014912.4 69 Intron NP_055727.3
XM_005269630.4 69 Intron XP_005269687.1
XM_006717714.3 69 Intron XP_006717777.1
XM_006717715.3 69 Intron XP_006717778.1
XM_011539514.2 69 Intron XP_011537816.1
XM_011539515.2 69 Intron XP_011537817.1
XM_011539517.2 69 Intron XP_011537819.1
XM_011539518.2 69 Intron XP_011537820.1
XM_011539519.2 69 Intron XP_011537821.1
XM_011539520.2 69 Intron XP_011537822.1
XM_011539522.2 69 Intron XP_011537824.1
XM_011539523.2 69 Intron XP_011537825.1
XM_017015927.1 69 Intron XP_016871416.1
Gene
MARCH5
Gene Name
membrane associated ring-CH-type finger 5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_017824.4 69 UTR 5 NP_060294.1
XM_011539886.2 69 UTR 5 XP_011538188.1

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