Product Details

SNP ID

rs16919376

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:93788092 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGACAGAGATGTGTGTTCTCTATGA[C/T]GTTCTCAGTATTGTTAGGGATAAAA

Phenotype

MIM: 603810

Polymorphism

C/T, Transition 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	617	Silent Mutation	GAC,GAT	D114D	NP_004259.3
XM_011543068.2	617	Silent Mutation	GAC,GAT	D114D	XP_011541370.1

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