Product Details

SNP ID

rs200537697

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:29673078 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGTGCTTGGTTCTTAAGTACAGATG[C/G]CTGGTTCTGGGCCATAGGACCCTCA

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	999	Intron			NP_001008229.1
NM_001008229.2	999	Intron			NP_001008230.1
NM_001170418.1	999	Intron			NP_001163889.1
NM_002433.4	999	Intron			NP_002424.3
NM_206809.3	999	Intron			NP_996532.2
NM_206810.3	999	Intron			NP_996533.2
NM_206811.3	999	Intron			NP_996534.2
NM_206812.3	999	Intron			NP_996535.2
NM_206814.5	999	Intron			NP_996537.3
XM_005249131.3	999	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	999	Missense Mutation	CCA,GCA	P345A	NP_001103279.2
XM_006715087.3	999	Missense Mutation	CCA,GCA	P273A	XP_006715150.1
XM_011514570.2	999	Missense Mutation	CCA,GCA	P345A	XP_011512872.1

View Full Product Details