Product Details

SNP ID

rs5981078

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:71150098 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCCTGAGCGCTTCTAATGCACACC[C/G]GAGCATGGAATGAGACCCGCTGCTG

Phenotype

MIM: 300188 MIM: 300336

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

MED12 PubMed Links

Gene Details

Gene

MED12

Gene Name

mediator complex subunit 12

There are no transcripts associated with this gene.

Gene

NLGN3

Gene Name

neuroligin 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001166660.1		Intron			NP_001160132.1
NM_001321276.1		Intron			NP_001308205.1
NM_018977.3		Intron			NP_061850.2
NM_181303.1		Intron			NP_851820.1

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