Product Details

SNP ID
rs56328668
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:61944017 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCACAAGGCTTAATTTCTCAAATAA[A/G]TCTACTGAGCTTTTCTAATGGTTAT
Phenotype
MIM: 603808
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
MED13 PubMed Links

Gene Details

Gene
MED13
Gene Name
mediator complex subunit 13
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_005121.2 8468 UTR 3 NP_005112.2
XM_011525551.2 8468 UTR 3 XP_011523853.1
XM_011525552.2 8468 Intron XP_011523854.1
XM_011525553.2 8468 UTR 3 XP_011523855.1

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