ClinVar Miner

List of variants in gene ALK reported as benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 50
Download table as spreadsheet
HGVS dbSNP
NM_004304.4(ALK):c.1110G>A (p.Glu370=) rs138784554
NM_004304.4(ALK):c.1128C>T (p.Leu376=) rs200396075
NM_004304.4(ALK):c.1234C>T (p.Arg412Cys) rs147102592
NM_004304.4(ALK):c.1427T>C (p.Val476Ala) rs35093491
NM_004304.4(ALK):c.1464C>T (p.Gly488=) rs56165377
NM_004304.4(ALK):c.1689C>T (p.Asn563=) rs565743321
NM_004304.4(ALK):c.1719C>T (p.Thr573=) rs74830770
NM_004304.4(ALK):c.1943C>T (p.Thr648Ile) rs116202066
NM_004304.4(ALK):c.2011C>T (p.Pro671Ser) rs145780832
NM_004304.4(ALK):c.2039C>T (p.Thr680Ile) rs35228363
NM_004304.4(ALK):c.2109C>T (p.Asn703=) rs560163657
NM_004304.4(ALK):c.2127C>A (p.Asn709Lys) rs376175333
NM_004304.4(ALK):c.2133C>T (p.Ser711=) rs77102810
NM_004304.4(ALK):c.2148C>T (p.Ser716=) rs55733526
NM_004304.4(ALK):c.2175C>T (p.Ile725=) rs57881134
NM_004304.4(ALK):c.2268C>T (p.Gly756=) rs149853746
NM_004304.4(ALK):c.2343C>T (p.Asp781=) rs61754933
NM_004304.4(ALK):c.2430C>T (p.Ser810=) rs150292405
NM_004304.4(ALK):c.2451C>T (p.Gly817=) rs183314518
NM_004304.4(ALK):c.2526C>T (p.Ala842=) rs145271283
NM_004304.4(ALK):c.2613C>T (p.Asn871=) rs150557024
NM_004304.4(ALK):c.2632+8G>A rs199653862
NM_004304.4(ALK):c.2676C>T (p.Ala892=) rs138668699
NM_004304.4(ALK):c.267C>A (p.Gly89=) rs192127241
NM_004304.4(ALK):c.2772T>G (p.Gly924=) rs749286400
NM_004304.4(ALK):c.2915-9T>C rs373765395
NM_004304.4(ALK):c.2928C>T (p.His976=) rs75895956
NM_004304.4(ALK):c.3035C>T (p.Thr1012Met) rs35073634
NM_004304.4(ALK):c.3057C>A (p.Val1019=) rs138406372
NM_004304.4(ALK):c.3336G>A (p.Pro1112=) rs146074150
NM_004304.4(ALK):c.3408C>T (p.Ser1136=) rs56146053
NM_004304.4(ALK):c.3594C>T (p.Leu1198=) rs56071005
NM_004304.4(ALK):c.3600G>A (p.Ala1200=) rs56247462
NM_004304.4(ALK):c.3600G>C (p.Ala1200=) rs56247462
NM_004304.4(ALK):c.3939-8A>G rs3738869
NM_004304.4(ALK):c.4203T>C (p.Tyr1401=) rs55772745
NM_004304.4(ALK):c.4303_4305delGAG (p.Glu1435del) rs138827116
NM_004304.4(ALK):c.4473G>A (p.Lys1491=) rs148987382
NM_004304.4(ALK):c.4480G>A (p.Gly1494Arg) rs199940609
NM_004304.4(ALK):c.4573A>G (p.Lys1525Glu) rs139437088
NM_004304.4(ALK):c.4596C>T (p.Asn1532=) rs1881422
NM_004304.4(ALK):c.4785C>T (p.Ala1595=) rs76150405
NM_004304.4(ALK):c.4836G>A (p.Lys1612=) rs78174819
NM_004304.4(ALK):c.487G>T (p.Val163Leu) rs55697431
NM_004304.4(ALK):c.592G>A (p.Val198Met) rs77677701
NM_004304.4(ALK):c.597C>T (p.Gly199=) rs200868013
NM_004304.4(ALK):c.645T>C (p.Leu215=) rs115392387
NM_004304.4(ALK):c.776G>A (p.Arg259His) rs138686378
NM_004304.4(ALK):c.846C>T (p.Asp282=) rs56116528
NM_004304.5(ALK):c.3837-9_3837-7dup rs373764155

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.