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

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Items: 52

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2396138	NM_005480.4(TROAP):c.116C>A (p.Ala39Asp)	TROAP, TROAP-AS1 (A39D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3183184	NM_005480.4(TROAP):c.179G>A (p.Arg60His)	TROAP, TROAP-AS1 (R60H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3183187	NM_005480.4(TROAP):c.223C>G (p.Gln75Glu)	TROAP, TROAP-AS1 (Q75E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3183188	NM_005480.4(TROAP):c.247G>A (p.Val83Met)	TROAP, TROAP-AS1 (V83M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3183189	NM_005480.4(TROAP):c.272C>T (p.Pro91Leu)	TROAP, TROAP-AS1 (P91L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623633	NM_005480.4(TROAP):c.332A>G (p.Gln111Arg)	TROAP, TROAP-AS1 (Q111R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379632	NM_005480.4(TROAP):c.352A>G (p.Ile118Val)	TROAP (I118V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3183190	NM_005480.4(TROAP):c.402G>T (p.Glu134Asp)	TROAP (E134D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467747	NM_005480.4(TROAP):c.428G>A (p.Arg143His)	TROAP (R143H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591441	NM_005480.4(TROAP):c.502C>T (p.Arg168Trp)	TROAP (R168W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473856	NM_005480.4(TROAP):c.503G>A (p.Arg168Gln)	TROAP (R168Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510834	NM_005480.4(TROAP):c.542G>A (p.Arg181Gln)	TROAP (R181Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375223	NM_005480.4(TROAP):c.596G>A (p.Arg199Gln)	TROAP (R199Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3183192	NM_005480.4(TROAP):c.717G>A (p.Arg239=)	TROAP	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2354188	NM_005480.4(TROAP):c.796G>A (p.Glu266Lys)	TROAP (E266K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599040	NM_005480.4(TROAP):c.803T>C (p.Val268Ala)	TROAP (V268A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547336	NM_005480.4(TROAP):c.811T>C (p.Ser271Pro)	TROAP (S271P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3183193	NM_005480.4(TROAP):c.982C>T (p.Arg328Trp)	TROAP (R328W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371930	NM_005480.4(TROAP):c.1066C>T (p.Arg356Trp)	TROAP (R356W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370069	NM_005480.4(TROAP):c.1067G>A (p.Arg356Gln)	TROAP (R356Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2467693	NM_005480.4(TROAP):c.1079T>C (p.Met360Thr)	TROAP (M360T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3183180	NM_005480.4(TROAP):c.1101G>C (p.Gln367His)	TROAP (Q367H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376665	NM_005480.4(TROAP):c.1118G>A (p.Arg373His)	TROAP (R373H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3183181	NM_005480.4(TROAP):c.1195G>A (p.Glu399Lys)	TROAP (E399K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317134	NM_005480.4(TROAP):c.1234C>T (p.Pro412Ser)	TROAP (P412S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332527	NM_005480.4(TROAP):c.1235C>T (p.Pro412Leu)	TROAP (P412L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523793	NM_005480.4(TROAP):c.1246C>T (p.Pro416Ser)	TROAP (P416S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317518	NM_005480.4(TROAP):c.1259A>T (p.His420Leu)	TROAP (H420L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485379	NM_005480.4(TROAP):c.1266C>A (p.Asn422Lys)	TROAP (N422K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3183182	NM_005480.4(TROAP):c.1303A>G (p.Ile435Val)	TROAP (I435V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527979	NM_005480.4(TROAP):c.1306G>A (p.Gly436Ser)	TROAP (G436S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2301103	NM_005480.4(TROAP):c.1339G>A (p.Glu447Lys)	TROAP (E447K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552131	NM_005480.4(TROAP):c.1466C>T (p.Ser489Phe)	TROAP (S489F)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2326192	NM_005480.4(TROAP):c.1491C>G (p.His497Gln)	TROAP (H497Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588664	NM_005480.4(TROAP):c.1550C>T (p.Pro517Leu)	TROAP (P517L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402649	NM_005480.4(TROAP):c.1557G>T (p.Glu519Asp)	TROAP (E519D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458953	NM_005480.4(TROAP):c.1600C>T (p.Pro534Ser)	TROAP (P534S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3183183	NM_005480.4(TROAP):c.1679G>A (p.Cys560Tyr)	TROAP (C560Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456647	NM_005480.4(TROAP):c.1700C>T (p.Pro567Leu)	TROAP (P567L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552924	NM_005480.4(TROAP):c.1712G>A (p.Arg571His)	TROAP (R571H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3183185	NM_005480.4(TROAP):c.1837C>T (p.Pro613Ser)	TROAP (P613S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325571	NM_005480.4(TROAP):c.1877C>T (p.Thr626Ile)	TROAP (T626I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332088	NM_005480.4(TROAP):c.1934A>G (p.Glu645Gly)	TROAP (E645G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384196	NM_005480.4(TROAP):c.1943C>A (p.Thr648Asn)	TROAP (T648N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556449	NM_005480.4(TROAP):c.2049C>A (p.Ser683Arg)	TROAP (S683R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368180	NM_005480.4(TROAP):c.2108A>G (p.Asn703Ser)	TROAP (N793S +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3183186	NM_005480.4(TROAP):c.2114C>T (p.Ala705Val)	TROAP (A795V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552132	NM_005480.4(TROAP):c.2144T>A (p.Leu715His)	TROAP (L715H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337141	NM_005480.4(TROAP):c.2161G>T (p.Ala721Ser)	TROAP (A721S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225232	NM_005480.4(TROAP):c.2242C>T (p.Arg748Trp)	TROAP (R748W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487138	NM_005480.4(TROAP):c.2321C>G (p.Pro774Arg)	TROAP (P864R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543246	NM_005480.4(TROAP):c.2323C>G (p.Gln775Glu)	TROAP (Q775E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 52