Product Details

SNP ID

rs142798897

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:6372544 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCTCCCCCCGGATGCTTCGATACT[C/T]AGCCATGTCTTCCGGAAATACTTTA

Phenotype

MIM: 612382

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MED10 PubMed Links

Gene Details

Gene

MED10

Gene Name

mediator complex subunit 10

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032286.2	410	Missense Mutation	AAG,GAG	K123E	NP_115662.2

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