Product Details

SNP ID
rs3802353
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:131863388 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GGGGGCGTGTGGAAGATTCCAGCAA[C/T]GGAAAGCCTGGCCAGGCTGGAGCAC
Phenotype
MIM: 605044
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
MED27 PubMed Links

Gene Details

Gene
MED27
Gene Name
mediator complex subunit 27
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001253881.1 Intron NP_001240810.1
NM_001253882.1 Intron NP_001240811.1
NM_004269.3 Intron NP_004260.2
XM_005272236.3 Intron XP_005272293.1
XM_017015329.1 Intron XP_016870818.1
XM_017015330.1 Intron XP_016870819.1

View Full Product Details