Product Details

SNP ID

rs143664908

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:71122179 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGTAACCATGGTGAATGAGTTGGAC[C/T]TAGCTGTTTCTATCTGGTAGACCAT

Phenotype

MIM: 300188

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MED12 PubMed Links

Gene Details

Gene

MED12

Gene Name

mediator complex subunit 12

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005120.2		Intron			NP_005111.2

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