Product Details

SNP ID
rs201532201
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:35295762 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTCTGGTACTTCAATAGCCCCTAC[C/G]CCAAGAACTACCCCCCGGTGGTCTT
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_001199216.1 394 Missense Mutation CCC,GCC P41A NP_001186145.1
NM_002361.3 394 Missense Mutation CCC,GCC P66A NP_002352.1
NM_080600.2 394 Missense Mutation CCC,GCC P66A NP_542167.1

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