List of variants in gene KIT reported as pathogenic for thymus 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000222.3(KIT):c.2089C>T (p.His697Tyr)	rs763308199	0.00010
NM_000222.3(KIT):c.1468G>A (p.Glu490Lys)	rs1057519701
NM_000222.3(KIT):c.1657T>A (p.Tyr553Asn)	rs1057519704
NM_000222.3(KIT):c.1669T>C (p.Trp557Arg)	rs121913235
NM_000222.3(KIT):c.1676T>C (p.Val559Ala)	rs121913517
NM_000222.3(KIT):c.1676TTG[1] (p.Val560del)	rs121913685
NM_000222.3(KIT):c.1727T>C (p.Leu576Pro)	rs121913513
NM_000222.3(KIT):c.1730_1738del (p.Pro577_Asp579del)	rs1131692239
NM_000222.3(KIT):c.2460T>A (p.Asp820Glu)	rs1057519711

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