APLN[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1257673	NM_017413.5(APLN):c.*5+186G>C	APLN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1275609	NM_017413.5(APLN):c.*5+62C>T	APLN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2400192	NM_017413.5(APLN):c.202C>T (p.Arg68Cys)	APLN (R68C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3127838	NM_017413.5(APLN):c.176G>A (p.Arg59Gln)	APLN (R59Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527386	NM_017413.5(APLN):c.89A>G (p.Asp30Gly)	APLN (D30G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1253078	NM_017413.5(APLN):c.67+151A>G	APLN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1272734	NM_017413.5(APLN):c.-314T>C	APLN	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign

ClinVar