Product Details

SNP ID

rs425729

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:117524401 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTAAGCATTTGTTTTAAAGAAGTGG[G/T]TCCTGGTATACACTAGATGTCCGTT

Phenotype

MIM: 610237

Polymorphism

G/T, 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		Intron			NP_001269915.1
NM_080651.3		Intron			NP_542382.1
XM_011517360.2		Intron			XP_011515662.1

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