List of variants in gene TPRN reported as likely pathogenic for not provided

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001128228.3(TPRN):c.1402dup (p.Gln468fs)	rs760851760
NM_001128228.3(TPRN):c.1964dup (p.Gly656fs)	rs1341134360
NM_001128228.3(TPRN):c.225_235dup (p.Leu79fs)	rs387906221

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