Product Details

SNP ID
rs200543468
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.X:23840348 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGCAGAGCATGGAGTTTTCTACTT[A/G]GTTCCAGGTGAATTCTTCACATTTC
Phenotype
MIM: 300753
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
APOO PubMed Links

Gene Details

Gene
APOO
Gene Name
apolipoprotein O
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_024122.4 1138 Intron NP_077027.1
XM_011545584.2 1138 Silent Mutation ACC,ACT T201T XP_011543886.1
XM_011545585.2 1138 Silent Mutation ACC,ACT T201T XP_011543887.1
XM_011545586.2 1138 Silent Mutation ACC,ACT T201T XP_011543888.1
XM_011545587.2 1138 Silent Mutation ACC,ACT T161T XP_011543889.1
XM_017029837.1 1138 Intron XP_016885326.1

View Full Product Details