"Ambry Genetics"[submitter] AND "ADAP2"[gene] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3080045	NM_018404.3(ADAP2):c.40C>G (p.Leu14Val)	ADAP2, LOC130060645 (L14V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3268693	NM_018404.3(ADAP2):c.100G>A (p.Asp34Asn)	ADAP2 (D34N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080020	NM_018404.3(ADAP2):c.211G>C (p.Asp71His)	ADAP2 (D71H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2620414	NM_018404.3(ADAP2):c.217A>G (p.Ile73Val)	ADAP2 (I73V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080029	NM_018404.3(ADAP2):c.229A>T (p.Met77Leu)	ADAP2 (M83L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2330906	NM_018404.3(ADAP2):c.251G>A (p.Arg84His)	ADAP2 (R84H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080034	NM_018404.3(ADAP2):c.258G>T (p.Lys86Asn)	ADAP2 (K92N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2486753	NM_018404.3(ADAP2):c.295A>C (p.Ile99Leu)	ADAP2 (I99L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080040	NM_018404.3(ADAP2):c.316C>G (p.Leu106Val)	ADAP2 (L106V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2550720	NM_018404.3(ADAP2):c.359G>A (p.Arg120Gln)	ADAP2 (R120Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2207892	NM_018404.3(ADAP2):c.434A>G (p.Asp145Gly)	ADAP2 (D145G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2481016	NM_018404.3(ADAP2):c.482G>T (p.Gly161Val)	ADAP2 (G161V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2344457	NM_018404.3(ADAP2):c.518G>T (p.Ser173Ile)	ADAP2 (S173I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3268709	NM_018404.3(ADAP2):c.650G>A (p.Ser217Asn)	ADAP2 (S217N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2314314	NM_018404.3(ADAP2):c.651T>A (p.Ser217Arg)	ADAP2 (S217R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3268702	NM_018404.3(ADAP2):c.665T>A (p.Val222Glu)	ADAP2 (V228E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2327162	NM_018404.3(ADAP2):c.686G>A (p.Arg229His)	ADAP2 (R235H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2341670	NM_018404.3(ADAP2):c.785T>C (p.Met262Thr)	ADAP2 (M268T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2511460	NM_018404.3(ADAP2):c.835G>A (p.Ala279Thr)	ADAP2 (A279T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2210341	NM_018404.3(ADAP2):c.892G>A (p.Glu298Lys)	ADAP2 (E297K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3268711	NM_018404.3(ADAP2):c.899G>T (p.Gly300Val)	ADAP2 (G299V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080072	NM_018404.3(ADAP2):c.929G>T (p.Gly310Val)	ADAP2 (G309V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3268685	NM_018404.3(ADAP2):c.964C>G (p.Arg322Gly)	ADAP2 (R328G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2470255	NM_018404.3(ADAP2):c.1018G>C (p.Val340Leu)	ADAP2 (V339L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2327329	NM_018404.3(ADAP2):c.1132C>A (p.Arg378Ser)	ADAP2 (R352S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 25