C__29707352_10

• SNP ID: rs9879808
• Gene: MOBP
• Gene Name: myelin-associated oligodendrocyte basic protein
• Set Membership: -
• Chromosome Location: Chr.3: 39479428 - 39479428 on Build GRCh38
• Polymorphism: C/T, Transition substitution
• Context Sequence [VIC/FAM]:

  TTTTTTCAAATAGCCCTTCTGAGAT[C/T]TGATATGTATTAATAAGGAATGGGA

Assay Details

Species:	Human
dbSNP Submissions:	NA
Phenotype:	MIM: 600948
Literature Links:	MOBP PubMed Links
Allele Nomenclature:
Minor Allele Frequency:

1000Genome	Applied Biosystems^®	HapMap
Global T (0.10) (0.90)	Caucasian - Not Available	CEPH (CEU) - Not Available
EAS - Not Available	African American - Not Available	YRI (Yoruba) - Not Available
SAS - Not Available	Chinese - Not Available	CHB (Han Chinese) - Not Available
AFR - Not Available	Japanese - Not Available	JPT (Japanese) - Not Available
EUR - Not Available
AMR - Not Available

MOBP - myelin-associated oligodendrocyte basic protein
Transcript Accession	SNP Location	SNP Type	Observed Codons	Observed Amino Acid	Protein ID
NM_001278322.1		Intron			NP_001265251.1
NM_001278323.1		Intron			NP_001265252.1
NM_182935.3		Intron			NP_891980.1

More Information

Panther Classification:

Molecular Function -

myelin protein

Gene Ontology Categories:

Process(es)

nervous system development

Function(s)

protein binding
structural constituent of myelin sheath