Product Details

SNP ID
rs201029431
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:135362939 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTAAATCTGTGGGGGTTTTGCTGGG[G/T]GGTCTGAAGGCTGTCTGAAAGCCTG
Phenotype
MIM: 604911
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
CNOT4 PubMed Links

Gene Details

Gene
CNOT4
Gene Name
CCR4-NOT transcription complex subunit 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001008225.2 2419 Intron NP_001008226.1
NM_001190847.1 2419 Silent Mutation CCA,CCC P625P NP_001177776.1
NM_001190848.1 2419 Intron NP_001177777.1
NM_001190849.1 2419 Silent Mutation CCA,CCC P693P NP_001177778.1
NM_001190850.1 2419 Silent Mutation CCA,CCC P696P NP_001177779.1
NM_013316.3 2419 Silent Mutation CCA,CCC P622P NP_037448.2
XM_017012235.1 2419 Silent Mutation CCA,CCC P696P XP_016867724.1

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