Product Details

SNP ID
rs202017359
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.19:35295650 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTCACTGGGGTGCCTGGATGCCCTC[A/G]TCCATCTCGGCCTTCGAAGGCACGT
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_001199216.1 282 Silent Mutation TCA,TCG S3S NP_001186145.1
NM_002361.3 282 Silent Mutation TCA,TCG S28S NP_002352.1
NM_080600.2 282 Silent Mutation TCA,TCG S28S NP_542167.1

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