Product Details

SNP ID
rs1043047
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:115959338 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTGTTTTTTTTCTTTTTCTGCTTA[A/G]AATTGGGTTTCTAGGGAAGAAAAGC
Phenotype
MIM: 608771
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
MED13L PubMed Links

Gene Details

Gene
MED13L
Gene Name
mediator complex subunit 13 like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_015335.4 8616 UTR 3 NP_056150.1
XM_011538080.2 8616 UTR 3 XP_011536382.1
XM_011538081.2 8616 UTR 3 XP_011536383.1
XM_011538082.2 8616 UTR 3 XP_011536384.1
XM_017019090.1 8616 UTR 3 XP_016874579.1

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