Product Details

SNP ID

rs11970677

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:41908544 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAAGCACATTTTTGCTTCCCAACCT[A/G]TCTTAAAGCATACTAAGGAAAGGTA

Phenotype

MIM: 612915

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

MED20 PubMed Links

Gene Details

Gene

MED20

Gene Name

mediator complex subunit 20

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001305455.1		Intron			NP_001292384.1
NM_001305456.1		Intron			NP_001292385.1
NM_001305457.1		Intron			NP_001292386.1
NM_004275.4		Intron			NP_004266.2

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