Product Details

SNP ID
rs144755172
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:36141384 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGCAAGGAAGATGCCTGAAGTGGTC[A/G]CACTCAGGATCCGGGCTCCTCTGCT
Phenotype
MIM: 607253
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
APOL3 PubMed Links

Gene Details

Gene
APOL3
Gene Name
apolipoprotein L3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_014349.2 1996 Missense Mutation GAG,GGG E271G NP_055164.1
NM_030644.1 1996 Missense Mutation GAG,GGG E271G NP_085147.1
NM_145639.1 1996 Missense Mutation GAG,GGG E271G NP_663614.1
NM_145640.2 1996 Missense Mutation GAG,GGG E342G NP_663615.1
NM_145641.2 1996 Missense Mutation GAG,GGG E142G NP_663616.1
NM_145642.2 1996 Missense Mutation GAG,GGG E142G NP_663617.1
XM_006724324.1 1996 Missense Mutation XP_006724387.1
XM_006724325.2 1996 Missense Mutation XP_006724388.1
XM_017028946.1 1996 Missense Mutation XP_016884435.1
XM_017028947.1 1996 Missense Mutation XP_016884436.1
XM_017028948.1 1996 Missense Mutation XP_016884437.1
XM_017028949.1 1996 Missense Mutation XP_016884438.1
XM_017028950.1 1996 Missense Mutation XP_016884439.1
XM_017028951.1 1996 Missense Mutation XP_016884440.1
XM_017028952.1 1996 Missense Mutation XP_016884441.1

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