"PreventionGenetics, part of Exact Sciences"[submitter] AND "APOL1"[ge - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1316241	NM_003661.4(APOL1):c.-20+739C>T	APOL1	Single nucleotide variant (5 prime UTR variant +1 more)	APOL1-related condition +1 more	GBenign/Likely benign
Select item 3031206	NM_003661.4(APOL1):c.-20+771T>C	APOL1	Single nucleotide variant (synonymous variant +1 more)	APOL1-related condition	GLikely benign
Select item 3034584	NM_003661.4(APOL1):c.-19-5T>C	APOL1	Single nucleotide variant (5 prime UTR variant +1 more)	APOL1-related condition	GLikely benign
Select item 3036562	NM_003661.4(APOL1):c.315-9C>T	APOL1	Single nucleotide variant (intron variant)	APOL1-related condition	GLikely benign
Select item 1299830	NM_003661.4(APOL1):c.318T>C (p.Asn106=)	APOL1	Single nucleotide variant (synonymous variant)	Focal segmental glomerulosclerosis 4, susceptibility to +2 more	GLikely benign
Select item 3046832	NM_003661.4(APOL1):c.528T>C (p.Asn176=)	APOL1	Single nucleotide variant (synonymous variant)	APOL1-related condition	GLikely benign
Select item 2744195	NM_003661.4(APOL1):c.534G>T (p.Val178=)	APOL1	Single nucleotide variant (synonymous variant)	APOL1-related condition +1 more	GLikely benign
Select item 1170849	NM_003661.4(APOL1):c.684G>A (p.Met228Ile)	APOL1 (M210I +2 more)	Single nucleotide variant (missense variant)	APOL1-related condition +1 more	GBenign
Select item 1170850	NM_003661.4(APOL1):c.764G>A (p.Arg255Lys)	APOL1 (R237K +2 more)	Single nucleotide variant (missense variant)	APOL1-related condition +1 more	GBenign
Select item 771542	NM_003661.4(APOL1):c.767A>G (p.Glu256Gly)	APOL1 (E238G +2 more)	Single nucleotide variant (missense variant)	APOL1-related condition +1 more	GBenign
Select item 731686	NM_003661.4(APOL1):c.809G>A (p.Gly270Asp)	APOL1 (G270D +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 666614	NM_003661.4(APOL1):c.960G>A (p.Arg320=)	APOL1	Single nucleotide variant (synonymous variant)	APOL1-related condition +2 more	GBenign
Select item 3034588	NM_003661.4(APOL1):c.1002G>A (p.Lys334=)	APOL1	Single nucleotide variant (synonymous variant)	APOL1-related condition	GLikely benign
Select item 1564116	NM_003661.4(APOL1):c.1092G>A (p.Lys364=)	APOL1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign