List of variants in gene ALK reported as likely benign for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 36

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HGVS	dbSNP	gnomAD frequency
NM_004304.5(ALK):c.1719C>T (p.Thr573=)	rs74830770	0.00577
NM_004304.5(ALK):c.3515+18C>T	rs79325200	0.00409
NM_004304.5(ALK):c.4836G>A (p.Lys1612=)	rs78174819	0.00363
NM_004304.5(ALK):c.3837-9_3837-7dup	rs373764155	0.00279
NM_004304.5(ALK):c.592G>A (p.Val198Met)	rs77677701	0.00221
NM_004304.5(ALK):c.2632+11dup	rs766699720	0.00205
NM_004304.5(ALK):c.1110G>A (p.Glu370=)	rs138784554	0.00195
NM_004304.5(ALK):c.3594C>T (p.Leu1198=)	rs56071005	0.00166
NM_004304.5(ALK):c.1817+11T>C	rs185559774	0.00139
NM_004304.5(ALK):c.4785C>T (p.Ala1595=)	rs76150405	0.00104
NM_004304.5(ALK):c.2148C>T (p.Ser716=)	rs55733526	0.00096
NM_004304.5(ALK):c.932G>A (p.Arg311His)	rs150966028	0.00063
NM_004304.5(ALK):c.3939-8A>G	rs3738869	0.00054
NM_004304.5(ALK):c.1234C>T (p.Arg412Cys)	rs147102592	0.00053
NM_004304.5(ALK):c.2451C>T (p.Gly817=)	rs183314518	0.00039
NM_004304.5(ALK):c.2633-4G>A	rs199575811	0.00031
NM_004304.5(ALK):c.3336G>A (p.Pro1112=)	rs146074150	0.00019
NM_004304.5(ALK):c.487G>T (p.Val163Leu)	rs55697431	0.00019
NM_004304.5(ALK):c.1626G>C (p.Pro542=)	rs143916398	0.00013
NM_004304.5(ALK):c.3173-11C>T	rs79339096	0.00013
NM_004304.5(ALK):c.3139G>A (p.Ala1047Thr)	rs370049091	0.00011
NM_004304.5(ALK):c.1752C>T (p.Val584=)	rs367912697	0.00009
NM_004304.5(ALK):c.4812C>T (p.Tyr1604=)	rs753750497	0.00008
NM_004304.5(ALK):c.-6G>A	rs778056023	0.00002
NM_004304.5(ALK):c.4480G>A (p.Gly1494Arg)	rs199940609	0.00002
NM_004304.5(ALK):c.102G>A (p.Ala34=)	rs561278614	0.00001
NM_004304.5(ALK):c.171C>T (p.Asp57=)	rs138165457	0.00001
NM_004304.5(ALK):c.2816-9G>A	rs200463420	0.00001
NM_004304.5(ALK):c.3123C>T (p.Thr1041=)	rs773260725	0.00001
NM_004304.5(ALK):c.3359+7G>A	rs778841767	0.00001
NM_004304.5(ALK):c.3091C>T (p.Leu1031=)	rs755537480
NM_004304.5(ALK):c.3120G>A (p.Val1040=)	rs1553394893
NM_004304.5(ALK):c.3172+12G>C	rs1271239593
NM_004304.5(ALK):c.3375C>T (p.Gly1125=)	rs3795850
NM_004304.5(ALK):c.4146G>A (p.Arg1382=)	rs1553387973
NM_004304.5(ALK):c.4297GAG[2] (p.Glu1435del)	rs138827116

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