Product Details

SNP ID
rs200930577
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:74095985 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGAATTTGCAGCTTCCTTCAAAAG[C/T]GTAAGTAATATCCCTTACCTACTGA
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
LIN52 PubMed Links

Gene Details

Gene
LIN52
Gene Name
lin-52 DREAM MuvB core complex component
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001024674.2 276 Silent Mutation AGC,AGT S48S NP_001019845.1
XM_011537320.2 276 Silent Mutation AGC,AGT S80S XP_011535622.1
XM_011537321.2 276 Silent Mutation AGC,AGT S80S XP_011535623.1
XM_011537322.2 276 Silent Mutation AGC,AGT S48S XP_011535624.2
XM_017021763.1 276 Silent Mutation AGC,AGT S46S XP_016877252.1
XM_017021764.1 276 Silent Mutation AGC,AGT S48S XP_016877253.1

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