Product Details

SNP ID

rs132619

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:36141623 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCATAACTTCCTTAAATACCTTCAA[G/T]CGGTCAATGCTGGTTGCAGTCAGCC

Phenotype

MIM: 607253

Polymorphism

G/T, Transversion 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	1757	Silent Mutation	CGA,CGC	R191R	NP_055164.1
NM_030644.1	1757	Silent Mutation	CGA,CGC	R191R	NP_085147.1
NM_145639.1	1757	Silent Mutation	CGA,CGC	R191R	NP_663614.1
NM_145640.2	1757	Silent Mutation	CGA,CGC	R262R	NP_663615.1
NM_145641.2	1757	Silent Mutation	CGA,CGC	R62R	NP_663616.1
NM_145642.2	1757	Silent Mutation	CGA,CGC	R62R	NP_663617.1
XM_006724324.1	1757	Silent Mutation	CGA,CGC	R191R	XP_006724387.1
XM_006724325.2	1757	Silent Mutation	CGA,CGC	R191R	XP_006724388.1
XM_017028946.1	1757	Silent Mutation	CGA,CGC	R192R	XP_016884435.1
XM_017028947.1	1757	Silent Mutation	CGA,CGC	R192R	XP_016884436.1
XM_017028948.1	1757	Silent Mutation	CGA,CGC	R192R	XP_016884437.1
XM_017028949.1	1757	Silent Mutation	CGA,CGC	R192R	XP_016884438.1
XM_017028950.1	1757	Silent Mutation	CGA,CGC	R192R	XP_016884439.1
XM_017028951.1	1757	Silent Mutation	CGA,CGC	R192R	XP_016884440.1
XM_017028952.1	1757	Silent Mutation	CGA,CGC	R62R	XP_016884441.1

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