NTSR2[gene] and "single gene"[properties] - ClinVar

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Items: 30

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2227763	NM_012344.4(NTSR2):c.1216C>A (p.Pro406Thr)	NTSR2 (P406T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2650686	NM_012344.4(NTSR2):c.1164G>A (p.Pro388=)	NTSR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2370825	NM_012344.4(NTSR2):c.1154G>A (p.Arg385Gln)	NTSR2 (R385Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488272	NM_012344.4(NTSR2):c.1153C>T (p.Arg385Trp)	NTSR2 (R385W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3301319	NM_012344.4(NTSR2):c.1117G>A (p.Val373Ile)	NTSR2 (V373I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202661	NM_012344.4(NTSR2):c.1116C>T (p.Ala372=)	NTSR2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3202659	NM_012344.4(NTSR2):c.1072T>C (p.Tyr358His)	NTSR2 (Y358H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379137	NM_012344.4(NTSR2):c.980C>T (p.Ala327Val)	NTSR2 (A327V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280380	NM_012344.4(NTSR2):c.976G>A (p.Asp326Asn)	NTSR2 (D326N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295201	NM_012344.4(NTSR2):c.913A>G (p.Met305Val)	NTSR2 (M305V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2603201	NM_012344.4(NTSR2):c.907G>A (p.Val303Met)	NTSR2 (V303M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311989	NM_012344.4(NTSR2):c.881G>A (p.Arg294His)	NTSR2 (R294H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3202666	NM_012344.4(NTSR2):c.860G>A (p.Arg287His)	NTSR2 (R287H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 782401	NM_012344.4(NTSR2):c.845G>A (p.Arg282Lys)	NTSR2 (R282K)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 738625	NM_012344.4(NTSR2):c.757C>A (p.Arg253Ser)	NTSR2 (R253S)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3301318	NM_012344.4(NTSR2):c.737C>T (p.Pro246Leu)	NTSR2 (P246L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3202665	NM_012344.4(NTSR2):c.652C>T (p.Pro218Ser)	NTSR2 (P218S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467231	NM_012344.4(NTSR2):c.589C>G (p.Leu197Val)	NTSR2 (L197V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238708	NM_012344.4(NTSR2):c.521T>C (p.Met174Thr)	NTSR2 (M174T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202664	NM_012344.4(NTSR2):c.457C>T (p.Arg153Trp)	NTSR2 (R153W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2606368	NM_012344.4(NTSR2):c.440T>C (p.Leu147Pro)	NTSR2 (L147P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493505	NM_012344.4(NTSR2):c.315C>G (p.Asp105Glu)	NTSR2 (D105E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512952	NM_012344.4(NTSR2):c.293A>G (p.His98Arg)	NTSR2 (H98R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204313	NM_012344.4(NTSR2):c.288G>T (p.Trp96Cys)	NTSR2 (W96C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2650687	NM_012344.4(NTSR2):c.192C>A (p.Arg64=)	NTSR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2457826	NM_012344.4(NTSR2):c.164A>G (p.His55Arg)	NTSR2 (H55R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202662	NM_012344.4(NTSR2):c.155T>C (p.Leu52Pro)	NTSR2 (L52P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332446	NM_012344.4(NTSR2):c.134T>C (p.Leu45Pro)	NTSR2 (L45P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552274	NM_012344.4(NTSR2):c.95A>T (p.Lys32Met)	NTSR2 (K32M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3301320	NM_012344.4(NTSR2):c.12C>A (p.Ser4Arg)	NTSR2 (S4R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 30