Product Details

SNP ID

rs184974475

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:29672639 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATGCTTCCATTCCTCCCCAGCCATA[C/G]TGGGGACATCATGAGAGAAGCCAAG

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	1438	Intron			NP_001008229.1
NM_001008229.2	1438	Intron			NP_001008230.1
NM_001170418.1	1438	Intron			NP_001163889.1
NM_002433.4	1438	Intron			NP_002424.3
NM_206809.3	1438	Intron			NP_996532.2
NM_206810.3	1438	Intron			NP_996533.2
NM_206811.3	1438	Intron			NP_996534.2
NM_206812.3	1438	Intron			NP_996535.2
NM_206814.5	1438	Intron			NP_996537.3
XM_005249131.3	1438	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	1438	Missense Mutation	ACT,AGT	T491S	NP_001103279.2
XM_006715087.3	1438	Missense Mutation	ACT,AGT	T419S	XP_006715150.1
XM_011514570.2	1438	Missense Mutation	ACT,AGT	T491S	XP_011512872.1

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