Product Details

SNP ID
rs147498582
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:82930966 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACTTTCCGCCTCCACTATTTAAAGC[A/T]GGTGTTGGCCTAGTAAGCAAGTCTG
Phenotype
MIM: 613367
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
LIN54 PubMed Links

Gene Details

Gene
LIN54
Gene Name
lin-54 DREAM MuvB core complex component
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001115007.2 1950 Silent Mutation CCA,CCT P454P NP_001108479.1
NM_001115008.2 1950 Silent Mutation CCA,CCT P454P NP_001108480.1
NM_001288996.1 1950 Silent Mutation CCA,CCT P586P NP_001275925.1
NM_001288997.1 1950 Silent Mutation CCA,CCT P454P NP_001275926.1
NM_194282.3 1950 Silent Mutation CCA,CCT P675P NP_919258.2
XM_005262750.4 1950 Silent Mutation CCA,CCT P675P XP_005262807.1
XM_006714081.3 1950 Silent Mutation CCA,CCT P675P XP_006714144.1
XM_017007728.1 1950 Silent Mutation CCA,CCT P586P XP_016863217.1
XM_017007729.1 1950 Silent Mutation CCA,CCT P274P XP_016863218.1
XM_017007730.1 1950 Silent Mutation CCA,CCT P274P XP_016863219.1

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