Product Details

SNP ID

rs4828122

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:85026668 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTAGAATTTTTTTTTCTACCAGATA[C/G]GCTAGGTCATCAGATCCCTAGGACA

Phenotype

MIM: 300955

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

APOOL PubMed Links

Gene Details

Gene

APOOL

Gene Name

apolipoprotein O like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_198450.5		Intron			NP_940852.3
XM_011530859.2		Intron			XP_011529161.1
XM_017029271.1		Intron			XP_016884760.1
XM_017029272.1		Intron			XP_016884761.1
XM_017029273.1		Intron			XP_016884762.1

View Full Product Details