"Ambry Genetics"[submitter] AND "NGFR-AS1"[gene] - ClinVar

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Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2325706	NM_002507.4(NGFR):c.328G>T (p.Ala110Ser)	NGFR, NGFR-AS1 (A110S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2402722	NM_002507.4(NGFR):c.348T>A (p.Asp116Glu)	NGFR, NGFR-AS1 (D116E)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2381148	NM_002507.4(NGFR):c.385G>A (p.Glu129Lys)	NGFR, NGFR-AS1 (E129K)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2254360	NM_002507.4(NGFR):c.410C>G (p.Ser137Cys)	NGFR, NGFR-AS1 (S137C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2296521	NM_002507.4(NGFR):c.514G>C (p.Asp172His)	NGFR, NGFR-AS1 (D172H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199183	NM_002507.4(NGFR):c.533G>T (p.Arg178Leu)	NGFR, NGFR-AS1 (R178L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321006	NM_002507.4(NGFR):c.544C>T (p.Arg182Cys)	NGFR, NGFR-AS1 (R182C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469075	NM_002507.4(NGFR):c.553G>A (p.Asp185Asn)	NGFR, NGFR-AS1 (D185N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320093	NM_002507.4(NGFR):c.565G>C (p.Glu189Gln)	NGFR, NGFR-AS1 (E189Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522454	NM_002507.4(NGFR):c.592C>T (p.Arg198Trp)	NGFR, NGFR-AS1 (R198W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380184	NM_002507.4(NGFR):c.601C>G (p.Pro201Ala)	NGFR, NGFR-AS1 (P201A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484675	NM_002507.4(NGFR):c.628C>T (p.Pro210Ser)	NGFR, NGFR-AS1 (P210S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302837	NM_002507.4(NGFR):c.635C>A (p.Thr212Asn)	NGFR, NGFR-AS1 (T212N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323035	NM_002507.4(NGFR):c.734G>A (p.Arg245Gln)	NGFR, NGFR-AS1 (R245Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299610	NM_002507.4(NGFR):c.740C>T (p.Thr247Ile)	NGFR, NGFR-AS1 (T247I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546751	NM_002507.4(NGFR):c.752T>C (p.Leu251Pro)	NGFR, NGFR-AS1 (L251P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199209	NM_002507.4(NGFR):c.862C>T (p.Arg288Trp)	NGFR, NGFR-AS1 (R288W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599881	NM_002507.4(NGFR):c.892G>A (p.Gly298Arg)	NGFR, NGFR-AS1 (G298R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247548	NM_002507.4(NGFR):c.892G>C (p.Gly298Arg)	NGFR, NGFR-AS1 (G298R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318967	NM_002507.4(NGFR):c.989A>G (p.Lys330Arg)	NGFR, NGFR-AS1 (K330R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299609	NM_002507.4(NGFR):c.991G>A (p.Gly331Ser)	NGFR, NGFR-AS1 (G331S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589198	NM_002507.4(NGFR):c.1151G>A (p.Arg384His)	NGFR, NGFR-AS1 (R384H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351700	NM_002507.4(NGFR):c.1184G>C (p.Ser395Thr)	NGFR, NGFR-AS1 (S395T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607454	NM_002507.4(NGFR):c.1197C>G (p.Asp399Glu)	NGFR, NGFR-AS1 (D399E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382150	NM_002507.4(NGFR):c.1198G>A (p.Ala400Thr)	NGFR, NGFR-AS1 (A400T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299607	NM_002507.4(NGFR):c.1216C>T (p.Arg406Cys)	NGFR, NGFR-AS1 (R406C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 26