"Ambry Genetics"[submitter] AND "LAG3"[gene] - ClinVar

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

Search results

Items: 52

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3117346	NM_002286.6(LAG3):c.89C>G (p.Pro30Arg)	LAG3 (P30R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3117335	NM_002286.6(LAG3):c.133A>G (p.Ser45Gly)	LAG3 (S45G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351225	NM_002286.6(LAG3):c.224C>A (p.Ala75Asp)	LAG3 (A75D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3289841	NM_002286.6(LAG3):c.226C>T (p.Pro76Ser)	LAG3 (P76S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319081	NM_002286.6(LAG3):c.227C>A (p.Pro76His)	LAG3 (P76H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343811	NM_002286.6(LAG3):c.235C>T (p.Pro79Ser)	LAG3 (P79S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3117339	NM_002286.6(LAG3):c.242C>T (p.Ala81Val)	LAG3 (A81V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3289844	NM_002286.6(LAG3):c.281C>G (p.Pro94Arg)	LAG3 (P94R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286995	NM_002286.6(LAG3):c.367G>T (p.Asp123Tyr)	LAG3, LOC130007274 (D123Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255580	NM_002286.6(LAG3):c.376G>A (p.Gly126Ser)	LAG3, LOC130007274 (G126S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3117340	NM_002286.6(LAG3):c.421C>T (p.Arg141Cys)	LAG3, LOC130007274 (R141C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364384	NM_002286.6(LAG3):c.476C>G (p.Ser159Cys)	LAG3, LOC130007274 (S159C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528484	NM_002286.6(LAG3):c.503A>G (p.Gln168Arg)	LAG3, LOC130007274 (Q168R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260189	NM_002286.6(LAG3):c.521G>A (p.Ser174Asn)	LAG3 (S174N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395787	NM_002286.6(LAG3):c.563A>G (p.Asn188Ser)	LAG3 (N188S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2307673	NM_002286.6(LAG3):c.587G>A (p.Arg196His)	LAG3 (R196H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3117341	NM_002286.6(LAG3):c.601C>T (p.His201Tyr)	LAG3 (H201Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588998	NM_002286.6(LAG3):c.611G>A (p.Arg204Gln)	LAG3 (R204Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216223	NM_002286.6(LAG3):c.616C>T (p.Arg206Trp)	LAG3 (R206W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281709	NM_002286.6(LAG3):c.628C>G (p.Arg210Gly)	LAG3 (R210G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549082	NM_002286.6(LAG3):c.647C>G (p.Ser216Cys)	LAG3 (S216C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370479	NM_002286.6(LAG3):c.650C>T (p.Pro217Leu)	LAG3 (P217L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305265	NM_002286.6(LAG3):c.660C>G (p.His220Gln)	LAG3 (H220Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279007	NM_002286.6(LAG3):c.664G>T (p.Ala222Ser)	LAG3 (A222S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252258	NM_002286.6(LAG3):c.775G>A (p.Val259Ile)	LAG3 (V259I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270082	NM_002286.6(LAG3):c.787G>A (p.Glu263Lys)	LAG3 (E263K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3117343	NM_002286.6(LAG3):c.814G>A (p.Ala272Thr)	LAG3 (A272T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2479584	NM_002286.6(LAG3):c.836G>A (p.Gly279Glu)	LAG3 (G279E)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2480332	NM_002286.6(LAG3):c.841C>T (p.Pro281Ser)	LAG3 (P281S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323298	NM_002286.6(LAG3):c.844T>C (p.Cys282Arg)	LAG3 (C282R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403169	NM_002286.6(LAG3):c.848G>A (p.Arg283His)	LAG3 (R283H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2352522	NM_002286.6(LAG3):c.872G>A (p.Arg291Gln)	LAG3 (R291Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3117344	NM_002286.6(LAG3):c.884C>T (p.Thr295Ile)	LAG3 (T295I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3117345	NM_002286.6(LAG3):c.890A>G (p.Lys297Arg)	LAG3 (K297R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213332	NM_002286.6(LAG3):c.1003A>G (p.Ile335Val)	LAG3 (I335V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2606159	NM_002286.6(LAG3):c.1030G>A (p.Ala344Thr)	LAG3 (A344T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3289839	NM_002286.6(LAG3):c.1040C>T (p.Thr347Ile)	LAG3 (T347I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3117334	NM_002286.6(LAG3):c.1112T>C (p.Val371Ala)	LAG3 (V371A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2323743	NM_002286.6(LAG3):c.1172G>A (p.Arg391Lys)	LAG3 (R391K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3289840	NM_002286.6(LAG3):c.1181C>T (p.Ser394Leu)	LAG3 (S394L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2322314	NM_002286.6(LAG3):c.1201C>G (p.Gln401Glu)	LAG3 (Q401E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2471752	NM_002286.6(LAG3):c.1254G>C (p.Glu418Asp)	LAG3 (E418D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3289843	NM_002286.6(LAG3):c.1270G>T (p.Ala424Ser)	LAG3 (A424S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2249924	NM_002286.6(LAG3):c.1307A>C (p.Gln436Pro)	LAG3 (Q355P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304596	NM_002286.6(LAG3):c.1415A>G (p.His472Arg)	LAG3 (H391R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597106	NM_002286.6(LAG3):c.1436G>A (p.Arg479Gln)	LAG3 (R398Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3117336	NM_002286.6(LAG3):c.1453G>A (p.Ala485Thr)	LAG3 (A485T +1 more)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 3117337	NM_002286.6(LAG3):c.1501G>A (p.Glu501Lys)	LAG3 (E501K +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3117338	NM_002286.6(LAG3):c.1507G>A (p.Glu503Lys)	LAG3 (E503K +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2380893	NM_002286.6(LAG3):c.1539A>T (p.Glu513Asp)	LAG3 (E513D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518135	NM_002286.6(LAG3):c.1541C>G (p.Pro514Arg)	LAG3 (P514R +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2204417	NM_002286.6(LAG3):c.1571A>G (p.Gln524Arg)	LAG3 (Q443R +1 more)	Single nucleotide variant (missense variant)	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: 52