Product Details

SNP ID
rs201907391
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:35295711 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCCTGCCGCTTTGACTTCCCGGAT[A/G]AGCTGCGGCCCGCTGTGGTGCATGG
Phenotype
MIM: 159460
Polymorphism
A/G, Transition 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_001199216.1 343 Missense Mutation AAG,GAG K24E NP_001186145.1
NM_002361.3 343 Missense Mutation AAG,GAG K49E NP_002352.1
NM_080600.2 343 Missense Mutation AAG,GAG K49E NP_542167.1

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