Product Details

SNP ID
rs112023970
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.18:76980839 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGTCAGCTAGAGGTGCCAGGGCAGC[C/T]GAGGGGAACTGCCAGCGACAACAGG
Phenotype
MIM: 159430
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
MBP PubMed Links

Gene Details

Gene
MBP
Gene Name
myelin basic protein
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001025081.1 Intron NP_001020252.1
NM_001025090.1 Intron NP_001020261.1
NM_001025092.1 Intron NP_001020263.1
NM_001025100.1 Intron NP_001020271.1
NM_001025101.1 Intron NP_001020272.1
NM_002385.2 Intron NP_002376.1
XM_011526009.2 Intron XP_011524311.1
XM_017025778.1 Intron XP_016881267.1
XM_017025779.1 Intron XP_016881268.1
XM_017025780.1 Intron XP_016881269.1

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