Product Details

SNP ID
rs200264212
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:36227659 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAACAACCCTCTCAACCTGTTCACC[G/T]CCTTCAGCTGAGATTCGCCCAATGA
Phenotype
MIM: 607252
Polymorphism
G/T, Transversion 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 1236 Intron NP_112092.2
NM_145637.2 1236 Silent Mutation NP_663612.2
XM_011530074.1 1236 Intron XP_011528376.1
XM_011530075.1 1236 Intron XP_011528377.1
XM_011530076.2 1236 Intron XP_011528378.1
XM_011530077.2 1236 Intron XP_011528379.1
XM_011530078.1 1236 Intron XP_011528380.1
XM_017028724.1 1236 Intron XP_016884213.1

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