Product Details

SNP ID
rs201222628
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:36228077 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGAGTTGGACACCACATTGGCAATG[A/G]TGGTGCCTCTGTGGACCTGCTCAAC
Phenotype
MIM: 607252
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
APOL2 PubMed Links

Gene Details

Gene
APOL2
Gene Name
apolipoprotein L2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_030882.3 818 Intron NP_112092.2
NM_145637.2 818 Missense Mutation ACC,ATC T114I NP_663612.2
XM_011530074.1 818 Intron XP_011528376.1
XM_011530075.1 818 Intron XP_011528377.1
XM_011530076.2 818 Intron XP_011528378.1
XM_011530077.2 818 Intron XP_011528379.1
XM_011530078.1 818 Intron XP_011528380.1
XM_017028724.1 818 Intron XP_016884213.1

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