List of variants in gene ALK reported by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_004304.5(ALK):c.4381A>G (p.Ile1461Val)	rs1670283	0.99030
NM_004304.5(ALK):c.27C>G (p.Leu9=)	rs4358080	0.88526
NM_004304.5(ALK):c.1500A>G (p.Gln500=)	rs2293564	0.79300
NM_004304.5(ALK):c.2535T>C (p.Gly845=)	rs2256740	0.63034
NM_004304.5(ALK):c.4587C>G (p.Asp1529Glu)	rs1881421	0.47503
NM_004304.5(ALK):c.3375C>A (p.Gly1125=)	rs3795850	0.27292
NM_004304.5(ALK):c.4472A>G (p.Lys1491Arg)	rs1881420	0.26767
NM_004304.5(ALK):c.3359+6C>T	rs4622670	0.24182
NM_004304.5(ALK):c.3594C>T (p.Leu1198=)	rs56071005	0.00166
NM_004304.5(ALK):c.4785C>T (p.Ala1595=)	rs76150405	0.00104
NM_004304.5(ALK):c.702T>A (p.Pro234=)	rs2246745

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.