ClinVar for Gene (Select 238) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3368654	NM_004304.5(ALK):c.787+4A>G	ALK	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 3363875	NM_004304.5(ALK):c.1750G>A (p.Val584Ile)	ALK (V584I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3361645	NM_004304.5(ALK):c.829T>C (p.Ser277Pro)	ALK (S277P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3359933	NM_004304.5(ALK):c.2050_2075del (p.Leu684fs)	ALK (L684fs)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 3345842	NM_004304.5(ALK):c.663_667+1dup	ALK	Duplication (splice donor variant)	ALK-related disorder	GUncertain significance
Select item 3343159	NM_004304.5(ALK):c.2914G>T (p.Val972Leu)	ALK (V972L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3343070	NM_004304.5(ALK):c.2281G>C (p.Gly761Arg)	ALK (G761R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3343060	NM_004304.5(ALK):c.1120G>C (p.Glu374Gln)	ALK (E374Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3343015	NM_004304.5(ALK):c.2138A>C (p.Glu713Ala)	ALK (E713A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3286688	NM_004304.5(ALK):c.1208C>T (p.Ala403Val)	ALK (A403V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3286677	NM_004304.5(ALK):c.3269C>A (p.Thr1090Asn)	ALK (T1090N +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3286610	NM_004304.5(ALK):c.3380T>G (p.Phe1127Cys)	ALK (F1127C +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3286592	NM_004304.5(ALK):c.738C>T (p.Thr246=)	ALK	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3286574	NM_004304.5(ALK):c.3246G>C (p.Lys1082Asn)	ALK (K1082N +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3286544	NM_004304.5(ALK):c.2045A>C (p.His682Pro)	ALK (H682P)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3286531	NM_004304.5(ALK):c.3736A>C (p.Ile1246Leu)	ALK (I1246L +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3286520	NM_004304.5(ALK):c.2984G>T (p.Cys995Phe)	ALK (C995F)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3286512	NM_004304.5(ALK):c.3659C>T (p.Ser1220Phe)	ALK (S1220F +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3286502	NM_004304.5(ALK):c.1236C>G (p.Arg412=)	ALK	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3286486	NM_004304.5(ALK):c.2991G>A (p.Met997Ile)	ALK (M997I)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3286465	NM_004304.5(ALK):c.26T>A (p.Leu9His)	ALK (L9H)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3286454	NM_004304.5(ALK):c.3132C>G (p.Leu1044=)	ALK	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3286434	NM_004304.5(ALK):c.2403A>G (p.Ile801Met)	ALK (I801M)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3286405	NM_004304.5(ALK):c.1733G>A (p.Gly578Asp)	ALK (G578D)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3286395	NM_004304.5(ALK):c.1743C>G (p.Val581=)	ALK	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3286375	NM_004304.5(ALK):c.4707A>C (p.Val1569=)	ALK	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3286364	NM_004304.5(ALK):c.108G>C (p.Pro36=)	ALK	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3286344	NM_004304.5(ALK):c.2890A>G (p.Ile964Val)	ALK (I964V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3286333	NM_004304.5(ALK):c.2490G>A (p.Met830Ile)	ALK (M830I)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3286323	NM_004304.5(ALK):c.3516-2A>G	ALK	Single nucleotide variant (splice acceptor variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3286304	NM_004304.5(ALK):c.1921G>A (p.Glu641Lys)	ALK (E641K)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3286293	NM_004304.5(ALK):c.2905G>A (p.Ala969Thr)	ALK (A969T)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3286267	NM_004304.5(ALK):c.64G>C (p.Gly22Arg)	ALK (G22R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3286260	NM_004304.5(ALK):c.2784C>T (p.Cys928=)	ALK	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3286251	NM_004304.5(ALK):c.4274T>C (p.Leu1425Pro)	ALK (L1425P +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3286240	NM_004304.5(ALK):c.4395C>T (p.Val1465=)	ALK	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3286220	NM_004304.5(ALK):c.728G>C (p.Trp243Ser)	ALK (W243S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3286201	NM_004304.5(ALK):c.966T>G (p.Leu322=)	ALK	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3286192	NM_004304.5(ALK):c.322G>C (p.Val108Leu)	ALK (V108L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3286184	NM_004304.5(ALK):c.2079C>G (p.Pro693=)	ALK	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3286166	NM_004304.5(ALK):c.1752C>A (p.Val584=)	ALK	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3286135	NM_004304.5(ALK):c.1244C>G (p.Ser415Cys)	ALK (S415C)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3286126	NM_004304.5(ALK):c.1427T>A (p.Val476Glu)	ALK (V476E)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3286117	NM_004304.5(ALK):c.4231G>A (p.Val1411Met)	ALK (V343M +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3286106	NM_004304.5(ALK):c.1179C>G (p.Ile393Met)	ALK (I393M)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3286095	NM_004304.5(ALK):c.4068G>A (p.Gly1356=)	ALK	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3286077	NM_004304.5(ALK):c.3761del (p.Asn1254fs)	ALK (N186fs +1 more)	Deletion (frameshift variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3286067	NM_004304.5(ALK):c.2540G>A (p.Arg847Lys)	ALK (R847K)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3286055	NM_004304.5(ALK):c.2700C>A (p.Ala900=)	ALK	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3286045	NM_004304.5(ALK):c.3016T>C (p.Cys1006Arg)	ALK (C1006R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3286034	NM_004304.5(ALK):c.2106C>T (p.Asn702=)	ALK	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3286014	NM_004304.5(ALK):c.4856G>A (p.Gly1619Glu)	ALK (G1619E +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3286003	NM_004304.5(ALK):c.2826A>G (p.Ala942=)	ALK	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3285998	NM_004304.5(ALK):c.2592C>T (p.Asn864=)	ALK	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3285979	NM_004304.5(ALK):c.2147G>A (p.Ser716Asn)	ALK (S716N)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285964	NM_004304.5(ALK):c.4073+3A>C	ALK	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285954	NM_004304.5(ALK):c.1401G>C (p.Glu467Asp)	ALK (E467D)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285944	NM_004304.5(ALK):c.97G>C (p.Ala33Pro)	ALK (A33P)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285936	NM_004304.5(ALK):c.972C>A (p.Asn324Lys)	ALK (N324K)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285929	NM_004304.5(ALK):c.4852C>A (p.Pro1618Thr)	ALK (P1618T +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285919	NM_004304.5(ALK):c.1012A>G (p.Met338Val)	ALK (M338V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285910	NM_004304.5(ALK):c.3119T>C (p.Val1040Ala)	ALK (V1040A)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285896	NM_004304.5(ALK):c.717T>C (p.Asp239=)	ALK	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3285885	NM_004304.5(ALK):c.3440T>A (p.Val1147Glu)	ALK (V79E +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285874	NM_004304.5(ALK):c.295C>A (p.Leu99Ile)	ALK (L99I)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285864	NM_004304.5(ALK):c.40C>G (p.Leu14Val)	ALK (L14V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285833	NM_004304.5(ALK):c.4204G>A (p.Gly1402Ser)	ALK (G1402S +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285823	NM_004304.5(ALK):c.4086G>A (p.Met1362Ile)	ALK (M294I +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285813	NM_004304.5(ALK):c.636G>A (p.Gln212=)	ALK	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3285794	NM_004304.5(ALK):c.3737T>C (p.Ile1246Thr)	ALK (I178T +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285785	NM_004304.5(ALK):c.1604C>G (p.Thr535Ser)	ALK (T535S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285767	NM_004304.5(ALK):c.2067G>A (p.Gly689=)	ALK	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3285759	NM_004304.5(ALK):c.4141del (p.Glu1381fs)	ALK (E313fs +1 more)	Deletion (frameshift variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285748	NM_004304.5(ALK):c.3424C>T (p.Pro1142Ser)	ALK (P74S +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285737	NM_004304.5(ALK):c.2722C>A (p.Gln908Lys)	ALK (Q908K)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285730	NM_004304.5(ALK):c.4688C>A (p.Thr1563Asn)	ALK (T1563N +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285723	NM_004304.5(ALK):c.2425A>G (p.Arg809Gly)	ALK (R809G)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285713	NM_004304.5(ALK):c.378G>A (p.Val126=)	ALK	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3285695	NM_004304.5(ALK):c.811C>A (p.Pro271Thr)	ALK (P271T)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285675	NM_004304.5(ALK):c.4236T>C (p.Pro1412=)	ALK	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3285665	NM_004304.5(ALK):c.302T>C (p.Leu101Ser)	ALK (L101S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285656	NM_004304.5(ALK):c.1965G>T (p.Leu655=)	ALK	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3285647	NM_004304.5(ALK):c.94C>A (p.Pro32Thr)	ALK (P32T)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285636	NM_004304.5(ALK):c.2781dup (p.Cys928fs)	ALK (C928fs)	Duplication (frameshift variant)	Hereditary cancer-predisposing syndrome	GBenign
Select item 3285606	NM_004304.5(ALK):c.3836+1G>T	ALK	Single nucleotide variant (splice donor variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285597	NM_004304.5(ALK):c.2042T>C (p.Val681Ala)	ALK (V681A)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285548	NM_004304.5(ALK):c.4333C>G (p.Pro1445Ala)	ALK (P1445A +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285458	NM_004304.5(ALK):c.3217C>G (p.Leu1073Val)	ALK (L1073V +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285422	NM_004304.5(ALK):c.1930A>G (p.Ile644Val)	ALK (I644V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285420	NM_004304.5(ALK):c.188T>C (p.Leu63Pro)	ALK (L63P)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285415	NM_004304.5(ALK):c.4597C>G (p.Leu1533Val)	ALK (L1533V +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285357	NM_004304.5(ALK):c.4278C>A (p.Val1426=)	ALK	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3285321	NM_004304.5(ALK):c.4181A>G (p.Asn1394Ser)	ALK (N326S +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285287	NM_004304.5(ALK):c.4106A>C (p.Gln1369Pro)	ALK (Q301P +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285237	NM_004304.5(ALK):c.2604A>G (p.Leu868=)	ALK	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3285221	NM_004304.5(ALK):c.2194G>T (p.Asp732Tyr)	ALK (D732Y)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285208	NM_004304.5(ALK):c.4068G>C (p.Gly1356=)	ALK	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3285167	NM_004304.5(ALK):c.1621G>A (p.Ala541Thr)	ALK (A541T)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3285115	NM_004304.5(ALK):c.4254T>C (p.Pro1418=)	ALK	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3285003	NM_004304.5(ALK):c.3907G>A (p.Glu1303Lys)	ALK (E235K +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance

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