Product Details

SNP ID
rs200563532
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.22:36227886 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGTCCAAGTTGCGGGCTTGGGCTC[A/G]TGCCCGCAATTTGTTTACTAGTTCT
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 1009 Intron NP_112092.2
NM_145637.2 1009 Nonsense Mutation CGA,TGA R178* NP_663612.2
XM_011530074.1 1009 Intron XP_011528376.1
XM_011530075.1 1009 Intron XP_011528377.1
XM_011530076.2 1009 Intron XP_011528378.1
XM_011530077.2 1009 Intron XP_011528379.1
XM_011530078.1 1009 Intron XP_011528380.1
XM_017028724.1 1009 Intron XP_016884213.1

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