Product Details

SNP ID

rs147636121

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:17477161 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCCTCAGCCGCCGCCGGTCCCTGC[A/G]CCTCAACCGCAGCAGTCGCCGGCGC

Phenotype

MIM: 609878

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

MED9 PubMed Links

Gene Details

Gene

MED9

Gene Name

mediator complex subunit 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018019.2	176	Silent Mutation	GCA,GCG	A40A	NP_060489.1

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