Product Details

SNP ID

rs17108246

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:70588275 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTTGGGAGTTGGTTTTTGGCCCTTG[A/G]ATGGTAAAAGAAATGGCTCAGGAAT

Phenotype

MIM: 602984

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

MED6 PubMed Links

Gene Details

Gene

MED6

Gene Name

mediator complex subunit 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001284209.1		Intron			NP_001271138.1
NM_001284210.1		Intron			NP_001271139.1
NM_001284211.1		Intron			NP_001271140.1
NM_005466.3		Intron			NP_005457.2

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