Product Details

SNP ID
rs201061871
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:35295701 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCGTCTCCATCCCCTGCCGCTTTGA[A/C]TTCCCGGATGAGCTGCGGCCCGCTG
Phenotype
MIM: 159460
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
MAG PubMed Links

Gene Details

Gene
MAG
Gene Name
myelin associated glycoprotein
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001199216.1 333 Missense Mutation GAA,GAC E20D NP_001186145.1
NM_002361.3 333 Missense Mutation GAA,GAC E45D NP_002352.1
NM_080600.2 333 Missense Mutation GAA,GAC E45D NP_542167.1

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