Product Details

SNP ID

rs11539353

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:93784611 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GATGGCACCGAGACGTACCTGCCCC[A/C]GCTGTCCATGTCGCAGAATCTGGCG

Phenotype

MIM: 603810

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

MED17 PubMed Links

Gene Details

Gene

MED17

Gene Name

mediator complex subunit 17

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004268.4	373	Missense Mutation	CAG,CCG	Q33P	NP_004259.3
XM_011543068.2	373	Missense Mutation	CAG,CCG	Q33P	XP_011541370.1

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