Product Details

SNP ID
rs141353102
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.6:41909470 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCCATTCTCAAAGAGGGCGAAACA[A/G]CTCAATGGGTACTCTGAGTTGTGCA
Phenotype
MIM: 612915
Polymorphism
A/G, 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_001305455.1 468 Silent Mutation AGC,AGT S12S NP_001292384.1
NM_001305456.1 468 Silent Mutation AGC,AGT S12S NP_001292385.1
NM_001305457.1 468 Silent Mutation AGC,AGT S74S NP_001292386.1
NM_004275.4 468 Silent Mutation AGC,AGT S74S NP_004266.2

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