Product Details

SNP ID
rs144923413
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:82931011 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGTCTGAAATTTGAGAGGATAACTT[C/T]GTCTTGGCTGCTGTTTGTTGCTGTA
Phenotype
MIM: 613367
Polymorphism
C/T, Transition 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 1905 Silent Mutation ACA,ACG T439T NP_001108479.1
NM_001115008.2 1905 Silent Mutation ACA,ACG T439T NP_001108480.1
NM_001288996.1 1905 Silent Mutation ACA,ACG T571T NP_001275925.1
NM_001288997.1 1905 Silent Mutation ACA,ACG T439T NP_001275926.1
NM_194282.3 1905 Silent Mutation ACA,ACG T660T NP_919258.2
XM_005262750.4 1905 Silent Mutation ACA,ACG T660T XP_005262807.1
XM_006714081.3 1905 Silent Mutation ACA,ACG T660T XP_006714144.1
XM_017007728.1 1905 Silent Mutation ACA,ACG T571T XP_016863217.1
XM_017007729.1 1905 Silent Mutation ACA,ACG T259T XP_016863218.1
XM_017007730.1 1905 Silent Mutation ACA,ACG T259T XP_016863219.1

View Full Product Details