ClinVar Miner

List of variants in gene ALK reported as benign by Sema4, Sema4

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_004304.5(ALK):c.1464C>T (p.Gly488=) rs56165377 0.00615
NM_004304.5(ALK):c.2268C>T (p.Gly756=) rs149853746 0.00304
NM_004304.5(ALK):c.3837-9_3837-7dup rs373764155 0.00279
NM_004304.5(ALK):c.1943C>T (p.Thr648Ile) rs116202066 0.00232
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.2915-9T>C rs373765395 0.00144
NM_004304.5(ALK):c.4785C>T (p.Ala1595=) rs76150405 0.00104
NM_004304.5(ALK):c.776G>A (p.Arg259His) rs138686378 0.00096
NM_004304.5(ALK):c.2613C>T (p.Asn871=) rs150557024 0.00093
NM_004304.5(ALK):c.2430C>T (p.Ser810=) rs150292405 0.00086
NM_004304.5(ALK):c.1277G>C (p.Ser426Thr) rs111796753 0.00054
NM_004304.5(ALK):c.1234C>T (p.Arg412Cys) rs147102592 0.00053
NM_004304.5(ALK):c.4255G>A (p.Glu1419Lys) rs56181542 0.00046
NM_004304.5(ALK):c.2451C>T (p.Gly817=) rs183314518 0.00039
NM_004304.5(ALK):c.1755C>T (p.Ala585=) rs373605278 0.00032
NM_004304.5(ALK):c.2633-4G>A rs199575811 0.00031
NM_004304.5(ALK):c.2526C>T (p.Ala842=) rs145271283 0.00029
NM_004304.5(ALK):c.3102G>A (p.Ser1034=) rs138771319 0.00029
NM_004304.5(ALK):c.310C>T (p.Pro104Ser) rs576431612 0.00026
NM_004304.5(ALK):c.4185C>T (p.Thr1395=) rs571470900 0.00022
NM_004304.5(ALK):c.487G>T (p.Val163Leu) rs55697431 0.00019
NM_004304.5(ALK):c.4407G>A (p.Pro1469=) rs372471601 0.00018
NM_004304.5(ALK):c.2478C>T (p.Tyr826=) rs142126984 0.00016
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.597C>T (p.Gly199=) rs200868013 0.00012
NM_004304.5(ALK):c.1111G>A (p.Ala371Thr) rs149968229 0.00011
NM_004304.5(ALK):c.1648-10G>A rs375646347 0.00011
NM_004304.5(ALK):c.2928C>T (p.His976=) rs75895956 0.00011
NM_004304.5(ALK):c.3139G>A (p.Ala1047Thr) rs370049091 0.00011
NM_004304.5(ALK):c.4473G>A (p.Lys1491=) rs148987382 0.00007
NM_004304.5(ALK):c.1689C>T (p.Asn563=) rs565743321 0.00005
NM_004304.5(ALK):c.4433T>C (p.Met1478Thr) rs141010693 0.00004
NM_004304.5(ALK):c.4425C>T (p.His1475=) rs139039449 0.00003
NM_004304.5(ALK):c.2265C>T (p.His755=) rs770603023 0.00002
NM_004304.5(ALK):c.768G>A (p.Leu256=) rs201536994 0.00001
NM_004304.5(ALK):c.3600G>A (p.Ala1200=) rs56247462
NM_004304.5(ALK):c.886G>A (p.Glu296Lys) rs56077855

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