Product Details

SNP ID
rs141082353
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:24405180 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATTTATTCTTCAGGTGAAGTGCACC[A/G]GTTTAGAACCTCTGACGTCTCTCAA
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
MRS2 PubMed Links

Gene Details

Gene
MRS2
Gene Name
MRS2, magnesium transporter
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001286264.1 342 Missense Mutation CAG,CGG Q68R NP_001273193.1
NM_001286265.1 342 Missense Mutation CAG,CGG Q68R NP_001273194.1
NM_001286266.1 342 Missense Mutation CAG,CGG Q68R NP_001273195.1
NM_020662.3 342 Missense Mutation CAG,CGG Q68R NP_065713.1
XM_005249242.1 342 Missense Mutation CAG,CGG Q68R XP_005249299.1

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