Product Details

SNP ID
rs187904565
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:32695666 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTAAAGACTGTCAAGGTTTGTGGGT[C/G]AAAGAGCTCTGTACGCATAGAAGGT
Phenotype
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
CNOT10 PubMed Links

Gene Details

Gene
CNOT10
Gene Name
CCR4-NOT transcription complex subunit 10
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001256741.1 133 Intron NP_001243670.1
NM_001256742.1 133 Nonsense Mutation TCA,TGA S14* NP_001243671.1
NM_015442.2 133 Intron NP_056257.1
XM_006713084.3 133 Nonsense Mutation TCA,TGA S14* XP_006713147.1
XM_006713085.3 133 Nonsense Mutation TCA,TGA S14* XP_006713148.1
XM_011533566.2 133 Nonsense Mutation TCA,TGA S14* XP_011531868.1
XM_011533567.2 133 Intron XP_011531869.1
XM_017006109.1 133 Intron XP_016861598.1
XM_017006110.1 133 Intron XP_016861599.1
XM_017006111.1 133 Intron XP_016861600.1
XM_017006112.1 133 Intron XP_016861601.1

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