Product Details

SNP ID

rs148324701

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:157138824 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTATGACCTGAATTTTCTCTTTGA[C/T]GTTCATTCTGTCCAGTACAATTGTT

Phenotype

MIM: 605045

Polymorphism

C/T, 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	716	Missense Mutation			NP_001094286.1
NM_004270.4	716	Missense Mutation			NP_004261.1

View Full Product Details