Product Details

SNP ID
rs7285167
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.22:36227874 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTGGTGCCGCTTTGGTCCAAGTTGC[A/G]GGCTTGGGCTCGTGCCCGCAATTTG
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 1021 Intron NP_112092.2
NM_145637.2 1021 Missense Mutation AGC,GGC S182G NP_663612.2
XM_011530074.1 1021 Intron XP_011528376.1
XM_011530075.1 1021 Intron XP_011528377.1
XM_011530076.2 1021 Intron XP_011528378.1
XM_011530077.2 1021 Intron XP_011528379.1
XM_011530078.1 1021 Intron XP_011528380.1
XM_017028724.1 1021 Intron XP_016884213.1

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