Product Details

SNP ID
rs997145
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:20512371 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GTAGACTCCTCCCCACCACTGTATT[C/T]ATGACTAGCTCCTTCTTTTAGGTGT
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 Intron NP_001003891.1
NM_001293234.1 Intron NP_001280163.1
NM_001293235.1 Intron NP_001280164.1
NM_001293236.1 Intron NP_001280165.1
NM_001293237.1 Intron NP_001280166.1
NM_015889.4 Intron NP_056973.2
XM_006724263.3 Intron XP_006724326.1
XM_006724264.3 Intron XP_006724327.1
XM_011530214.2 Intron XP_011528516.1
XM_011530215.2 Intron XP_011528517.1
XM_011530218.2 Intron XP_011528520.1
XM_011530219.1 Intron XP_011528521.1
XM_011530220.2 Intron XP_011528522.1
XM_017028817.1 Intron XP_016884306.1
XM_017028818.1 Intron XP_016884307.1
XM_017028819.1 Intron XP_016884308.1
XM_017028820.1 Intron XP_016884309.1
XM_017028821.1 Intron XP_016884310.1
XM_017028822.1 Intron XP_016884311.1
XM_017028823.1 Intron XP_016884312.1
XM_017028824.1 Intron XP_016884313.1

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