Product Details

SNP ID
rs113961195
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:41907166 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CATGGTATCTGCTGGGCCGTAGACC[A/G]CATCATGTCTGTTCCCAAACACTGC
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_001305455.1 791 Missense Mutation GCG,GTG A120V NP_001292384.1
NM_001305456.1 791 Missense Mutation GCG,GTG A120V NP_001292385.1
NM_001305457.1 791 UTR 3 NP_001292386.1
NM_004275.4 791 Missense Mutation GCG,GTG A182V NP_004266.2

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