List of variants in gene TMPRSS3 reported as pathogenic by GeneDx

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001256317.3(TMPRSS3):c.413C>A (p.Ala138Glu)	rs147231991	0.00146
NM_001256317.3(TMPRSS3):c.1273G>A (p.Ala425Thr)	rs56264519	0.00108
NM_001256317.3(TMPRSS3):c.916G>A (p.Ala306Thr)	rs181949335	0.00019
NM_001256317.3(TMPRSS3):c.325C>T (p.Arg109Trp)	rs201632198	0.00009
NM_001256317.3(TMPRSS3):c.46C>T (p.Arg16Ter)	rs976363536	0.00001
NM_001256317.3(TMPRSS3):c.1008del (p.Val337fs)	rs774670393
NM_001256317.3(TMPRSS3):c.1206del (p.Leu404fs)	rs1235521923
NM_001256317.3(TMPRSS3):c.1216T>C (p.Cys406Arg)	rs773780151
NM_001256317.3(TMPRSS3):c.208del (p.His70fs)	rs727503493
NM_001256317.3(TMPRSS3):c.323-6G>A	rs374793617

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