List of variants in gene NUMA1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_006185.4(NUMA1):c.1430A>G (p.Asn477Ser)	rs145185561	0.00288
NM_006185.4(NUMA1):c.981G>A (p.Leu327=)	rs143260427	0.00051
NM_006185.4(NUMA1):c.1033A>T (p.Thr345Ser)
NM_006185.4(NUMA1):c.1505C>G (p.Ser502Cys)
NM_006185.4(NUMA1):c.2752C>T (p.Arg918Cys)
NM_006185.4(NUMA1):c.3587G>A (p.Arg1196His)

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