Product Details

SNP ID

rs184914659

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:93784737 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCGCAGGAGTGGCCGGGCGCCGGGT[C/G]CAGCGCAGACCAGGACGACGAGGAA

Phenotype

MIM: 603810

Polymorphism

C/G, 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	499	Missense Mutation	TCC,TGC	S75C	NP_004259.3
XM_011543068.2	499	Missense Mutation	TCC,TGC	S75C	XP_011541370.1

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