Product Details

SNP ID

rs36073794

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:157138869 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTGTTGCTATCATCAGCATCCATT[A/G]GTTCAGTTTTTACTCTCATTCCTGC

Phenotype

MIM: 605045

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

MED7 PubMed Links

Gene Details

Gene

MED7

Gene Name

mediator complex subunit 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001100816.1	671	Missense Mutation	CCA,CTA	P188L	NP_001094286.1
NM_004270.4	671	Missense Mutation	CCA,CTA	P188L	NP_004261.1

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