Product Details

SNP ID
rs75946839
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:20508261 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGTGACCCCCCGAAGGAATGTGGA[C/T]TTTGCCGAAGGATGGCAGGAAGCCG
Phenotype
MIM: 607372
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
MED15 PubMed Links

Gene Details

Gene
MED15
Gene Name
mediator complex subunit 15
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001003891.2 214 Intron NP_001003891.1
NM_001293234.1 214 Intron NP_001280163.1
NM_001293235.1 214 Intron NP_001280164.1
NM_001293236.1 214 Intron NP_001280165.1
NM_001293237.1 214 UTR 5 NP_001280166.1
NM_015889.4 214 Intron NP_056973.2
XM_006724263.3 214 Intron XP_006724326.1
XM_006724264.3 214 Intron XP_006724327.1
XM_011530214.2 214 Intron XP_011528516.1
XM_011530215.2 214 Intron XP_011528517.1
XM_011530218.2 214 Intron XP_011528520.1
XM_011530219.1 214 Intron XP_011528521.1
XM_011530220.2 214 Intron XP_011528522.1
XM_017028817.1 214 Intron XP_016884306.1
XM_017028818.1 214 Intron XP_016884307.1
XM_017028819.1 214 Intron XP_016884308.1
XM_017028820.1 214 Intron XP_016884309.1
XM_017028821.1 214 Intron XP_016884310.1
XM_017028822.1 214 Intron XP_016884311.1
XM_017028823.1 214 Intron XP_016884312.1
XM_017028824.1 214 Intron XP_016884313.1

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