List of variants in gene TARDBP reported as pathogenic 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_007375.4(TARDBP):c.1144G>A (p.Ala382Thr)	rs367543041	0.00003
NM_007375.4(TARDBP):c.1009A>G (p.Met337Val)	rs80356730	0.00001
NM_007375.4(TARDBP):c.1042G>T (p.Gly348Cys)	rs80356733
NM_007375.4(TARDBP):c.1055A>G (p.Asn352Ser)	rs80356734
NM_007375.4(TARDBP):c.943G>A (p.Ala315Thr)	rs80356726

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