ClinVar Miner

List of variants in gene NONO studied for X-linked disease

Included ClinVar conditions (275):
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Gene type:
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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_007363.5(NONO):c.154+11G>C rs142366840 0.01069
NM_007363.5(NONO):c.107C>T (p.Pro36Leu) rs750695677 0.00001
NM_007363.5(NONO):c.107del (p.Pro36fs) rs1602385860
NM_007363.5(NONO):c.1093C>T (p.Arg365Ter) rs869025345
NM_007363.5(NONO):c.1131G>A (p.Ala377=) rs869025343
NM_007363.5(NONO):c.1171+1G>T rs876661316
NM_007363.5(NONO):c.1171G>T (p.Gly391Cys) rs1114167441
NM_007363.5(NONO):c.1191_1192del (p.Asn397fs) rs2031508845
NM_007363.5(NONO):c.1242del (p.Gly415fs) rs2148040741
NM_007363.5(NONO):c.1394dup (p.Asn466fs) rs869025344
NM_007363.5(NONO):c.154+1GT[2]
NM_007363.5(NONO):c.201_202dup (p.Lys68fs) rs2148033408
NM_007363.5(NONO):c.276_288del (p.Lys92fs)
NM_007363.5(NONO):c.279_282del (p.Phe94fs) rs2148033495
NM_007363.5(NONO):c.298_307del (p.Ala100fs)
NM_007363.5(NONO):c.315_318del (p.His106fs) rs2148033533
NM_007363.5(NONO):c.322_348+280del rs2148033540
NM_007363.5(NONO):c.457C>T (p.Arg153Ter) rs2031389522
NM_007363.5(NONO):c.550C>T (p.Arg184Ter) rs1602387702
NM_007363.5(NONO):c.651-1G>C rs2031456898
NM_007363.5(NONO):c.731dup (p.Asn244fs) rs1555950011
NM_007363.5(NONO):c.809G>T (p.Arg270Leu)

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