Product Details

SNP ID
rs140356022
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:41907215 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCGGGAGCCCCTGGTGTGTGGCTGC[C/T]TAGAAAACTCTGTAGGAACTCGAGC
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_001305455.1 742 Missense Mutation AGC,GGC S104G NP_001292384.1
NM_001305456.1 742 Missense Mutation AGC,GGC S104G NP_001292385.1
NM_001305457.1 742 UTR 3 NP_001292386.1
NM_004275.4 742 Missense Mutation AGC,GGC S166G NP_004266.2

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