"Ambry Genetics"[submitter] AND "LATS1"[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 34

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2363344	NM_004690.4(LATS1):c.3332C>T (p.Ser1111Leu)	LATS1 (S1111L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3117943	NM_004690.4(LATS1):c.3040G>A (p.Asp1014Asn)	LATS1 (D1014N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2463091	NM_004690.4(LATS1):c.2693C>T (p.Ala898Val)	LATS1 (A618V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2524212	NM_004690.4(LATS1):c.2630A>G (p.Asn877Ser)	LATS1 (N597S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3117942	NM_004690.4(LATS1):c.2605C>T (p.Arg869Trp)	LATS1 (R589W +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2532654	NM_004690.4(LATS1):c.2476C>A (p.His826Asn)	LATS1 (H546N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2288121	NM_004690.4(LATS1):c.2137A>G (p.Ile713Val)	LATS1 (I608V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3117941	NM_004690.4(LATS1):c.1937A>G (p.His646Arg)	LATS1 (H541R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3117940	NM_004690.4(LATS1):c.1888C>T (p.Arg630Cys)	LATS1 (R630C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2244677	NM_004690.4(LATS1):c.1811A>G (p.Asp604Gly)	LATS1 (D499G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2261174	NM_004690.4(LATS1):c.1681A>G (p.Lys561Glu)	LATS1 (K456E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2463454	NM_004690.4(LATS1):c.1669C>T (p.Pro557Ser)	LATS1 (P277S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3117939	NM_004690.4(LATS1):c.1657C>G (p.Gln553Glu)	LATS1 (Q273E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2611632	NM_004690.4(LATS1):c.1543A>G (p.Thr515Ala)	LATS1 (T235A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2298175	NM_004690.4(LATS1):c.1505G>A (p.Arg502His)	LATS1 (R397H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3117938	NM_004690.4(LATS1):c.1247G>A (p.Ser416Asn)	LATS1 (S311N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3117936	NM_004690.4(LATS1):c.1202C>T (p.Thr401Ile)	LATS1 (T121I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2386131	NM_004690.4(LATS1):c.1183G>A (p.Ala395Thr)	LATS1 (A115T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2261336	NM_004690.4(LATS1):c.1130C>A (p.Pro377His)	LATS1 (P272H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3117935	NM_004690.4(LATS1):c.1108C>T (p.Arg370Trp)	LATS1 (R90W +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2291065	NM_004690.4(LATS1):c.1105A>G (p.Asn369Asp)	LATS1 (N89D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3117948	NM_004690.4(LATS1):c.988A>G (p.Ile330Val)	LATS1 (I330V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2307725	NM_004690.4(LATS1):c.853A>G (p.Ile285Val)	LATS1 (I285V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3117947	NM_004690.4(LATS1):c.836G>T (p.Gly279Val)	LATS1 (G174V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3117946	NM_004690.4(LATS1):c.826C>T (p.Arg276Cys)	LATS1 (R171C +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2455924	NM_004690.4(LATS1):c.752C>T (p.Pro251Leu)	LATS1 (P146L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3117945	NM_004690.4(LATS1):c.749C>T (p.Pro250Leu)	LATS1 (P145L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2288746	NM_004690.4(LATS1):c.658A>T (p.Ile220Leu)	LATS1 (I220L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2299764	NM_004690.4(LATS1):c.630T>G (p.Asp210Glu)	LATS1 (D210E +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3117944	NM_004690.4(LATS1):c.613C>T (p.Pro205Ser)	LATS1 (P100S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2402416	NM_004690.4(LATS1):c.521G>A (p.Arg174His)	LATS1 (R69H +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2472294	NM_004690.4(LATS1):c.475A>G (p.Ile159Val)	LATS1 (I54V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3117934	NM_004690.4(LATS1):c.100A>G (p.Ile34Val)	LATS1 (I34V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2338596	NM_004690.4(LATS1):c.82C>G (p.Arg28Gly)	LATS1 (R28G)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 34