Product Details

SNP ID

rs140164059

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:36141550 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTTCACTCCCAATGGTTTGTGTGG[C/T]TTCGTAATAATTATTAAGAAGGGAA

Phenotype

MIM: 607253

Polymorphism

C/T, 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	1830	Missense Mutation	ACC,GCC	T216A	NP_055164.1
NM_030644.1	1830	Missense Mutation	ACC,GCC	T216A	NP_085147.1
NM_145639.1	1830	Missense Mutation	ACC,GCC	T216A	NP_663614.1
NM_145640.2	1830	Missense Mutation	ACC,GCC	T287A	NP_663615.1
NM_145641.2	1830	Missense Mutation	ACC,GCC	T87A	NP_663616.1
NM_145642.2	1830	Missense Mutation	ACC,GCC	T87A	NP_663617.1
XM_006724324.1	1830	Missense Mutation	ACC,GCC	T216A	XP_006724387.1
XM_006724325.2	1830	Missense Mutation	ACC,GCC	T216A	XP_006724388.1
XM_017028946.1	1830	Missense Mutation	ACC,GCC	T217A	XP_016884435.1
XM_017028947.1	1830	Missense Mutation	ACC,GCC	T217A	XP_016884436.1
XM_017028948.1	1830	Missense Mutation	ACC,GCC	T217A	XP_016884437.1
XM_017028949.1	1830	Missense Mutation	ACC,GCC	T217A	XP_016884438.1
XM_017028950.1	1830	Missense Mutation	ACC,GCC	T217A	XP_016884439.1
XM_017028951.1	1830	Missense Mutation	ACC,GCC	T217A	XP_016884440.1
XM_017028952.1	1830	Missense Mutation	ACC,GCC	T87A	XP_016884441.1

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