"Ambry Genetics"[submitter] AND "LENG8"[gene] - ClinVar

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

Search results

Items: 51

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2366821	NM_052925.4(LENG8):c.26G>A (p.Arg9His)	LENG8 (R9H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2408504	NM_052925.4(LENG8):c.92C>T (p.Thr31Met)	LENG8 (T13M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290469	NM_052925.4(LENG8):c.164C>T (p.Ala55Val)	LENG8 (A55V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597301	NM_052925.4(LENG8):c.169G>A (p.Gly57Ser)	LENG8 (G39S +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2461414	NM_052925.4(LENG8):c.191A>G (p.Asn64Ser)	LENG8 (N46S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118362	NM_052925.4(LENG8):c.194G>T (p.Gly65Val)	LENG8 (G65V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374506	NM_052925.4(LENG8):c.224A>G (p.Gln75Arg)	LENG8 (Q57R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118365	NM_052925.4(LENG8):c.320T>C (p.Met107Thr)	LENG8 (M89T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2243030	NM_052925.4(LENG8):c.397G>A (p.Ala133Thr)	LENG8 (A115T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2236179	NM_052925.4(LENG8):c.439G>A (p.Gly147Ser)	LENG8 (G110S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118366	NM_052925.4(LENG8):c.467C>T (p.Ala156Val)	LENG8 (A156V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541702	NM_052925.4(LENG8):c.512A>T (p.Asn171Ile)	LENG8 (N153I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285948	NM_052925.4(LENG8):c.557G>C (p.Gly186Ala)	LENG8 (G149A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206491	NM_052925.4(LENG8):c.559A>C (p.Thr187Pro)	LENG8 (T187P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118367	NM_052925.4(LENG8):c.595G>A (p.Ala199Thr)	LENG8 (A199T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290468	NM_052925.4(LENG8):c.631G>A (p.Glu211Lys)	LENG8 (E211K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296706	NM_052925.4(LENG8):c.635C>G (p.Pro212Arg)	LENG8 (P194R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2298256	NM_052925.4(LENG8):c.643C>T (p.Pro215Ser)	LENG8 (P215S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290470	NM_052925.4(LENG8):c.644C>A (p.Pro215His)	LENG8 (P197H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384879	NM_052925.4(LENG8):c.698G>A (p.Gly233Asp)	LENG8 (G233D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228429	NM_052925.4(LENG8):c.725C>A (p.Pro242His)	LENG8 (P205H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470499	NM_052925.4(LENG8):c.737C>A (p.Thr246Asn)	LENG8 (T228N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290464	NM_052925.4(LENG8):c.770A>G (p.Gln257Arg)	LENG8 (Q239R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118356	NM_052925.4(LENG8):c.1007G>A (p.Ser336Asn)	LENG8 (S299N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408792	NM_052925.4(LENG8):c.1065G>T (p.Lys355Asn)	LENG8 (K355N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247544	NM_052925.4(LENG8):c.1066C>T (p.Arg356Trp)	LENG8 (R319W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409609	NM_052925.4(LENG8):c.1074G>T (p.Glu358Asp)	LENG8 (E321D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306908	NM_052925.4(LENG8):c.1106C>T (p.Ala369Val)	LENG8 (A332V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304479	NM_052925.4(LENG8):c.1175G>A (p.Arg392Gln)	LENG8 (R374Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118357	NM_052925.4(LENG8):c.1221C>G (p.Phe407Leu)	LENG8 (F370L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118358	NM_052925.4(LENG8):c.1237T>C (p.Ser413Pro)	LENG8 (S376P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315382	NM_052925.4(LENG8):c.1259G>A (p.Arg420His)	LENG8 (R383H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530432	NM_052925.4(LENG8):c.1378C>G (p.Pro460Ala)	LENG8 (P442A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220106	NM_052925.4(LENG8):c.1387C>T (p.Arg463Trp)	LENG8 (R426W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118359	NM_052925.4(LENG8):c.1430C>T (p.Ala477Val)	LENG8 (A477V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524257	NM_052925.4(LENG8):c.1514G>A (p.Arg505Gln)	LENG8 (R468Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2601803	NM_052925.4(LENG8):c.1565G>A (p.Arg522His)	LENG8 (R522H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118360	NM_052925.4(LENG8):c.1661G>T (p.Cys554Phe)	LENG8 (C517F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376367	NM_052925.4(LENG8):c.1752C>G (p.Cys584Trp)	LENG8 (C547W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290467	NM_052925.4(LENG8):c.1859C>T (p.Thr620Met)	LENG8 (T602M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223569	NM_052925.4(LENG8):c.1954G>A (p.Ala652Thr)	LENG8 (A634T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340225	NM_052925.4(LENG8):c.2053T>A (p.Tyr685Asn)	LENG8 (Y648N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290466	NM_052925.4(LENG8):c.2062C>G (p.Arg688Gly)	LENG8 (R651G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549356	NM_052925.4(LENG8):c.2126G>A (p.Gly709Asp)	LENG8 (G709D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287445	NM_052925.4(LENG8):c.2164C>T (p.Pro722Ser)	LENG8 (P704S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118363	NM_052925.4(LENG8):c.2180A>G (p.Tyr727Cys)	LENG8 (Y690C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359202	NM_052925.4(LENG8):c.2215G>C (p.Val739Leu)	LENG8 (V721L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290463	NM_052925.4(LENG8):c.2252C>T (p.Ala751Val)	LENG8 (A751V)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3118364	NM_052925.4(LENG8):c.2309G>A (p.Arg770Gln)	LENG8 (R770Q)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2508066	NM_052925.4(LENG8):c.2348C>T (p.Pro783Leu)	LENG8 (P783L)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2345733	NM_052925.4(LENG8):c.2387A>G (p.Gln796Arg)	LENG8 (Q796R)	Single nucleotide variant (3 prime UTR variant +1 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: 51