Product Details

SNP ID
rs9883677
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:151092758 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAAAGAGGAGGCAAGGGAGATACTT[C/G]ATTTCAGAAAGCTCCTCACCTGAGA
Phenotype
MIM: 611318
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
MED12L PubMed Links

Gene Details

Gene
MED12L
Gene Name
mediator complex subunit 12 like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_053002.5 Intron NP_443728.3
XM_006713487.3 Intron XP_006713550.1
XM_011512390.2 Intron XP_011510692.1
XM_011512394.2 Intron XP_011510696.1
XM_011512399.2 Intron XP_011510701.1
XM_017005676.1 Intron XP_016861165.1
XM_017005677.1 Intron XP_016861166.1
XM_017005678.1 Intron XP_016861167.1
XM_017005679.1 Intron XP_016861168.1
XM_017005680.1 Intron XP_016861169.1
XM_017005681.1 Intron XP_016861170.1

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