Product Details

SNP ID

rs3130250

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.6:29657224 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

GAACAGTAGAGATGGCAAGCTTATC[A/G]AGACCCTCTCTGCCCAGCTGCCTCT

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	244	Silent Mutation	TCA,TCG	S5S	NP_001008229.1
NM_001008229.2	244	Silent Mutation	TCA,TCG	S5S	NP_001008230.1
NM_001170418.1	244	Silent Mutation	TCA,TCG	S5S	NP_001163889.1
NM_002433.4	244	Silent Mutation	TCA,TCG	S5S	NP_002424.3
NM_206809.3	244	Silent Mutation	TCA,TCG	S5S	NP_996532.2
NM_206810.3	244	Silent Mutation	TCA,TCG	S5S	NP_996533.2
NM_206811.3	244	Silent Mutation	TCA,TCG	S5S	NP_996534.2
NM_206812.3	244	Silent Mutation	TCA,TCG	S5S	NP_996535.2
NM_206814.5	244	Silent Mutation	TCA,TCG	S5S	NP_996537.3
XM_005249131.3	244	Silent Mutation	TCA,TCG	S5S	XP_005249188.1

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