List of variants in gene ALK reported as uncertain significance for central nervous system neoplasm

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_004304.5(ALK):c.1283-5T>C	rs377214413	0.00012
NM_004304.5(ALK):c.1550A>G (p.His517Arg)	rs367674546	0.00008
NM_004304.5(ALK):c.3115G>A (p.Val1039Met)	rs200080181	0.00007
NM_004304.5(ALK):c.3160G>A (p.Gly1054Ser)	rs375889530	0.00007
NM_004304.5(ALK):c.2633-3C>T	rs200341945	0.00006
NM_004304.5(ALK):c.2194G>A (p.Asp732Asn)	rs768366852	0.00003
NM_004304.5(ALK):c.1582G>A (p.Ala528Thr)	rs758494304	0.00002
NM_004304.5(ALK):c.1193A>G (p.Asn398Ser)	rs754512910	0.00001
NM_004304.5(ALK):c.3271G>A (p.Asp1091Asn)	rs864309584	0.00001
NM_004304.5(ALK):c.623T>C (p.Ile208Thr)	rs372226787	0.00001
NM_004304.5(ALK):c.1517T>C (p.Leu506Pro)	rs762569153
NM_004304.5(ALK):c.164C>A (p.Ala55Glu)	rs1217013970
inv(2)(p23.1p23.2)

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