Product Details

SNP ID
rs199797593
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:117520969 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGCCGCCCGGGAAGTCAACACGGC[G/T]TCGCTGTGCCGCATCGGGCAGGAGA
Phenotype
MIM: 610237
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
MED30 PubMed Links

Gene Details

Gene
MED30
Gene Name
mediator complex subunit 30
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001282986.1 424 Silent Mutation GCG,GCT A31A NP_001269915.1
NM_080651.3 424 Silent Mutation GCG,GCT A31A NP_542382.1
XM_011517360.2 424 Silent Mutation GCG,GCT A31A XP_011515662.1

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