List of variants in gene NONO reported as pathogenic for not provided

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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_007363.5(NONO):c.1009C>T (p.Arg337Ter)	rs1085307870
NM_007363.5(NONO):c.103C>T (p.Gln35Ter)	rs1057524408
NM_007363.5(NONO):c.1071dup (p.Gln358fs)
NM_007363.5(NONO):c.1131G>A (p.Ala377=)	rs869025343
NM_007363.5(NONO):c.1289del (p.Pro430fs)	rs1064796806
NM_007363.5(NONO):c.217C>T (p.Arg73Ter)	rs1555949215
NM_007363.5(NONO):c.230_231del (p.Phe77fs)	rs1057518476
NM_007363.5(NONO):c.245del (p.Pro82fs)	rs1602386427
NM_007363.5(NONO):c.550C>T (p.Arg184Ter)	rs1602387702

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