List of variants in gene NPM1 reported as uncertain significance for connective tissue 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_002520.7(NPM1):c.*101T>C	rs530255077
NM_002520.7(NPM1):c.*1del	rs2113301429
NM_002520.7(NPM1):c.*29A>T	rs200638434
NM_002520.7(NPM1):c.*2A>G	rs2113301446
NM_002520.7(NPM1):c.*33T>C	rs2113301714
NM_002520.7(NPM1):c.*73T>C	rs2113302170
NM_002520.7(NPM1):c.*75C>T	rs2113302182
NM_002520.7(NPM1):c.*76T>C	rs2113302197
NM_002520.7(NPM1):c.*80T>A	rs2113302213
NM_002520.7(NPM1):c.*81A>T	rs1271696160
NM_002520.7(NPM1):c.*98C>T	rs2113302335
NR_149149.2(NPM1):n.858_859del	rs2113301411

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