Product Details

SNP ID

rs200284390

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:29659393 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGATGAAGTGGAATTGCCATGTCGC[A/G]TATCTCCTGGGAAGAACGCTACAGG

Phenotype

MIM: 159465

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

MOG PubMed Links

Gene Details

Gene

MOG

Gene Name

myelin oligodendrocyte glycoprotein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001008228.2	392	Missense Mutation	ATA,GTA	I55V	NP_001008229.1
NM_001008229.2	392	Missense Mutation	ATA,GTA	I55V	NP_001008230.1
NM_001170418.1	392	Intron			NP_001163889.1
NM_002433.4	392	Missense Mutation	ATA,GTA	I55V	NP_002424.3
NM_206809.3	392	Missense Mutation	ATA,GTA	I55V	NP_996532.2
NM_206810.3	392	Missense Mutation	ATA,GTA	I55V	NP_996533.2
NM_206811.3	392	Missense Mutation	ATA,GTA	I55V	NP_996534.2
NM_206812.3	392	Missense Mutation	ATA,GTA	I55V	NP_996535.2
NM_206814.5	392	Intron			NP_996537.3
XM_005249131.3	392	Missense Mutation	ATA,GTA	I55V	XP_005249188.1

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