Product Details

SNP ID
rs200052512
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:41907090 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTCATCACTAACGAATCCCAGCCAC[C/T]GGCACCTGCTGCTGCTTGCGGATCT
Phenotype
MIM: 612915
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
MED20 PubMed Links

Gene Details

Gene
MED20
Gene Name
mediator complex subunit 20
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001305455.1 867 Silent Mutation CCA,CCG P145P NP_001292384.1
NM_001305456.1 867 Silent Mutation CCA,CCG P145P NP_001292385.1
NM_001305457.1 867 UTR 3 NP_001292386.1
NM_004275.4 867 Silent Mutation CCA,CCG P207P NP_004266.2

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