List of variants in gene NPM1 reported as pathogenic for bone cancer

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_002520.7(NPM1):c.860_863dup (p.Trp288fs)	rs587776806
NM_002520.7(NPM1):c.863_864insCATG (p.Trp288fs)	rs1554138188
NM_002520.7(NPM1):c.863_864insCCTG (p.Trp288fs)	rs1554138189
NM_002520.7(NPM1):c.863_864insCGTG (p.Trp288fs)	rs1554138188
NM_002520.7(NPM1):c.864_873delinsTTTAAGGATTCGTC (p.Trp288fs)	rs1581263026
NM_002520.7(NPM1):c.869_875delinsCCCTGGCTAGG (p.Trp290fs)	rs1561878500
NM_002520.7(NPM1):c.875del (p.Lys292fs)	rs2113301331
NM_002520.7(NPM1):c.885A>G (p.Ter295=)	rs2113301391

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