Product Details

SNP ID

rs139672719

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:117520952 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGGGCCCCAGGCTCAGCAGGCCGCC[A/C]GGGAAGTCAACACGGCGTCGCTGTG

Phenotype

MIM: 610237

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

MED30 PubMed Links

Gene Details

Gene

MED30

Gene Name

mediator complex subunit 30

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001282986.1	407	Silent Mutation	AGG,CGG	R26R	NP_001269915.1
NM_080651.3	407	Silent Mutation	AGG,CGG	R26R	NP_542382.1
XM_011517360.2	407	Silent Mutation	AGG,CGG	R26R	XP_011515662.1

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