"Ambry Genetics"[submitter] AND "AGAP2-AS1"[gene] - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2288358	NM_001122772.3(AGAP2):c.3496A>G (p.Ser1166Gly)	AGAP2, AGAP2-AS1 (S810G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518696	NM_001122772.3(AGAP2):c.3482C>T (p.Ala1161Val)	AGAP2, AGAP2-AS1 (A1161V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385819	NM_001122772.3(AGAP2):c.3473C>G (p.Thr1158Arg)	AGAP2, AGAP2-AS1 (T802R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225001	NM_001122772.3(AGAP2):c.3370G>A (p.Gly1124Ser)	AGAP2, AGAP2-AS1 (G1124S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339191	NM_001122772.3(AGAP2):c.3310G>A (p.Val1104Ile)	AGAP2, AGAP2-AS1 (V748I +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2295929	NM_001122772.3(AGAP2):c.3308A>G (p.His1103Arg)	AGAP2, AGAP2-AS1 (H747R +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2306358	NM_001122772.3(AGAP2):c.3198C>G (p.Asp1066Glu)	AGAP2, AGAP2-AS1 (D1066E +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2533753	NM_001122772.3(AGAP2):c.3161T>C (p.Leu1054Pro)	AGAP2, AGAP2-AS1 (L1054P +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2478420	NM_001122772.3(AGAP2):c.3140T>G (p.Leu1047Arg)	AGAP2, AGAP2-AS1 (L691R +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2249878	NM_001122772.3(AGAP2):c.3013G>T (p.Asp1005Tyr)	AGAP2, AGAP2-AS1 (D1005Y +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2309833	NM_001122772.3(AGAP2):c.2969A>T (p.Asp990Val)	AGAP2, AGAP2-AS1 (D990V +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3093737	NM_001122772.3(AGAP2):c.2834T>C (p.Ile945Thr)	AGAP2, AGAP2-AS1 (I945T +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2540332	NM_001122772.3(AGAP2):c.2822A>T (p.Lys941Met)	AGAP2, AGAP2-AS1 (K585M +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3093727	NM_001122772.3(AGAP2):c.2729T>C (p.Leu910Pro)	AGAP2, AGAP2-AS1 (L554P +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance