"Ambry Genetics"[submitter] AND "APLNR"[gene] - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2258789	NM_005161.6(APLNR):c.922C>G (p.Leu308Val)	APLNR (L308V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2360919	NM_005161.6(APLNR):c.884C>A (p.Thr295Asn)	APLNR (T295N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2252676	NM_005161.6(APLNR):c.811T>G (p.Tyr271Asp)	APLNR (Y271D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3127848	NM_005161.6(APLNR):c.730C>T (p.Arg244Cys)	APLNR (R244C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3127847	NM_005161.6(APLNR):c.721C>T (p.Arg241Trp)	APLNR (R241W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3127846	NM_005161.6(APLNR):c.697C>T (p.Arg233Cys)	APLNR (R233C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3127845	NM_005161.6(APLNR):c.669C>A (p.Phe223Leu)	APLNR (F223L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2531004	NM_005161.6(APLNR):c.631G>T (p.Val211Leu)	APLNR (V211L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2612845	NM_005161.6(APLNR):c.622G>T (p.Val208Leu)	APLNR (V208L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3127844	NM_005161.6(APLNR):c.611C>T (p.Ser204Leu)	APLNR (S204L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2474482	NM_005161.6(APLNR):c.540G>T (p.Gln180His)	APLNR (Q180H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2406523	NM_005161.6(APLNR):c.530C>T (p.Thr177Ile)	APLNR (T177I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3127843	NM_005161.6(APLNR):c.511G>A (p.Gly171Arg)	APLNR (G171R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3127842	NM_005161.6(APLNR):c.452C>A (p.Ala151Glu)	APLNR (A151E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2588667	NM_005161.6(APLNR):c.442G>A (p.Val148Met)	APLNR (V148M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2204570	NM_005161.6(APLNR):c.428G>A (p.Arg143Gln)	APLNR (R143Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2321173	NM_005161.6(APLNR):c.358C>A (p.Leu120Ile)	APLNR (L120I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2467861	NM_005161.6(APLNR):c.349G>A (p.Val117Ile)	APLNR (V117I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3127841	NM_005161.6(APLNR):c.343G>A (p.Ala115Thr)	APLNR (A115T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2235522	NM_005161.6(APLNR):c.332T>C (p.Val111Ala)	APLNR (V111A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2527602	NM_005161.6(APLNR):c.331G>A (p.Val111Ile)	APLNR (V111I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2521129	NM_005161.6(APLNR):c.271C>T (p.Arg91Trp)	APLNR (R91W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2398595	NM_005161.6(APLNR):c.242C>T (p.Thr81Met)	APLNR (T81M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3127839	NM_005161.6(APLNR):c.235G>A (p.Val79Met)	APLNR (V79M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 24