Product Details

SNP ID
rs149889819
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.19:54143156 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTGCCTCAAGAAGGTGTCCGAGGG[C/T]GTGGAGCAGTTTGAAGATATTTGGC
Phenotype
MIM: 604910
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
CNOT3 PubMed Links

Gene Details

Gene
CNOT3
Gene Name
CCR4-NOT transcription complex subunit 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_014516.3 421 Silent Mutation GGC,GGT G21G NP_055331.1
XM_005278279.1 421 Silent Mutation GGC,GGT G21G XP_005278336.1
XM_005278280.2 421 Silent Mutation GGC,GGT G21G XP_005278337.1
XM_005278281.1 421 Silent Mutation GGC,GGT G21G XP_005278338.1
XM_005278282.2 421 Silent Mutation GGC,GGT G21G XP_005278339.1
XM_011526992.1 421 Silent Mutation GGC,GGT G21G XP_011525294.1
XM_011526993.2 421 Silent Mutation GGC,GGT G21G XP_011525295.1

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