Product Details

SNP ID

rs200369502

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:29673240 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTGGAATCCTCAAAGTACACTCCT[C/G]GTTTCCATCCACTGGCTCCTGGTTT

Phenotype

MIM: 159465 MIM: 612192

Polymorphism

C/G, Transversion 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	837	Intron			NP_001008229.1
NM_001008229.2	837	Intron			NP_001008230.1
NM_001170418.1	837	Intron			NP_001163889.1
NM_002433.4	837	Intron			NP_002424.3
NM_206809.3	837	Intron			NP_996532.2
NM_206810.3	837	Intron			NP_996533.2
NM_206811.3	837	Intron			NP_996534.2
NM_206812.3	837	Intron			NP_996535.2
NM_206814.5	837	Intron			NP_996537.3
XM_005249131.3	837	Intron			XP_005249188.1

Gene

ZFP57

Gene Name

ZFP57 zinc finger protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001109809.2	837	Missense Mutation	CAG,GAG	Q291E	NP_001103279.2
XM_006715087.3	837	Missense Mutation	CAG,GAG	Q219E	XP_006715150.1
XM_011514570.2	837	Missense Mutation	CAG,GAG	Q291E	XP_011512872.1

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