Product Details

SNP ID
rs200065531
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:35295716 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCGCTTTGACTTCCCGGATGAGCT[C/G]CGGCCCGCTGTGGTGCATGGTGTCT
Phenotype
MIM: 159460
Polymorphism
C/G, 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_001199216.1 348 Silent Mutation CTC,CTG L25L NP_001186145.1
NM_002361.3 348 Silent Mutation CTC,CTG L50L NP_002352.1
NM_080600.2 348 Silent Mutation CTC,CTG L50L NP_542167.1

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