Product Details

SNP ID

rs4908397

Assay Type

Functionally tested

NCBI dbSNP Submissions

7

Location

Chr.1:28329208 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTGCTTCTAGTGTTTAATTGGATAC[A/G]TGTTATGGATGCCGGCTTAGAAGGA

Phenotype

MIM: 612384

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

MED18 PubMed Links

Gene Details

Gene

MED18

Gene Name

mediator complex subunit 18

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001127350.1		Intron			NP_001120822.1
NM_017638.2		Intron			NP_060108.2
XM_005245914.4		Intron			XP_005245971.1

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