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SNP ID

rs148750770

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:16576414 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACAGCTCCTTCCAGTTCGTCTGTTC[A/G]AAGGGGCTCTGGAGGCTGGCCTTGG

Phenotype

MIM: 605043

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

MED26 PubMed Links

Gene Details

Gene

MED26

Gene Name

mediator complex subunit 26

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004831.3	1677	Silent Mutation	TTC,TTT	F472F	NP_004822.2

Gene

SLC35E1

Gene Name

solute carrier family 35 member E1

There are no transcripts associated with this gene.

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