Product Details

SNP ID
rs147359880
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:16576182 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGGCCTGGATTCTGTCGAGATCGT[C/T]CTGTGTGACCTCCCGGGTCAGACCA
Phenotype
MIM: 605043
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
MED26 PubMed Links

Gene Details

Gene
MED26
Gene Name
mediator complex subunit 26
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_004831.3 1909 Missense Mutation AAC,GAC N550D NP_004822.2
Gene
SLC35E1
Gene Name
solute carrier family 35 member E1
There are no transcripts associated with this gene.

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