List of variants in gene ALK reported as likely pathogenic for embryonal neoplasm

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_004304.5(ALK):c.3749T>C (p.Ile1250Thr)	rs113994092	0.00001
NM_004304.5(ALK):c.3383G>C (p.Gly1128Ala)	rs113994088
NM_004304.5(ALK):c.3497T>G (p.Met1166Arg)	rs1057520019
NM_004304.5(ALK):c.3520T>C (p.Phe1174Leu)	rs281864719
NM_004304.5(ALK):c.3522C>G (p.Phe1174Leu)	rs863225281
NM_004304.5(ALK):c.3575G>C (p.Arg1192Pro)	rs113994089
NM_004304.5(ALK):c.3718T>G (p.Leu1240Val)	rs863225282
NM_004304.5(ALK):c.3733T>A (p.Phe1245Ile)	rs281864720
NM_004304.5(ALK):c.3733T>C (p.Phe1245Leu)	rs281864720
NM_004304.5(ALK):c.3824G>T (p.Arg1275Leu)	rs113994087

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