Product Details

SNP ID

rs16889828

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:117524160 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGTGAAATCTGTGATCACTCATCCA[A/G]GACCCTTTGGGGCCTATCATAATTG

Phenotype

MIM: 610237

Polymorphism

A/G, Transition 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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