ClinVar Miner

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

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Gene type:
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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_007363.5(NONO):c.1132-73T>C rs112643329 0.06947
NM_007363.5(NONO):c.363A>G (p.Leu121=) rs61733878 0.03765
NM_007363.5(NONO):c.747-10T>C rs35702657 0.02536
NM_007363.5(NONO):c.154+150G>C rs5980751 0.01804
NM_007363.5(NONO):c.154+11G>C rs142366840 0.01069
NM_007363.5(NONO):c.1029-15G>A rs12007473 0.00920
NM_007363.5(NONO):c.1179G>T (p.Met393Ile) rs138148374 0.00444
NM_007363.5(NONO):c.650+7G>A rs200412300 0.00094
NM_007363.5(NONO):c.573C>T (p.Gly191=) rs140307297 0.00051
NM_007363.5(NONO):c.1029-4G>C rs200784440 0.00024
NM_007363.5(NONO):c.1131+8T>C rs199640347 0.00020
NM_007363.5(NONO):c.1029-8C>T
NM_007363.5(NONO):c.1132-10dup
NM_007363.5(NONO):c.1210G>A (p.Ala404Thr)
NM_007363.5(NONO):c.1282-19CT[2] rs764838305
NM_007363.5(NONO):c.1282-2dup rs750124873
NM_007363.5(NONO):c.349-14C>T
NM_007363.5(NONO):c.447C>T (p.Ser149=)
NM_007363.5(NONO):c.642G>C (p.Leu214=)
NM_007363.5(NONO):c.650+187G>C rs112470710
NM_007363.5(NONO):c.864C>T (p.Asn288=)
NM_007363.5(NONO):c.943+18A>C
NM_007363.5(NONO):c.944-3del
NM_007363.5(NONO):c.944-3dup

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