Product Details

SNP ID

rs149323845

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:61943057 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACTCCACAAAAAAGAAAATACATAC[A/G]TAAAAATTTAAACCACAGTTCTGGG

Phenotype

MIM: 603808

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

MED13 PubMed Links

Gene Details

Gene

MED13

Gene Name

mediator complex subunit 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005121.2	9428	UTR 3			NP_005112.2
XM_011525551.2	9428	UTR 3			XP_011523853.1
XM_011525552.2	9428	Intron			XP_011523854.1
XM_011525553.2	9428	UTR 3			XP_011523855.1

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