List of variants in gene TNC reported as uncertain significance for auditory system disorder

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_002160.4(TNC):c.2374G>T (p.Gly792Cys)	rs150868783	0.00131
NM_002160.4(TNC):c.6211G>A (p.Glu2071Lys)	rs140573419	0.00036
NM_002160.4(TNC):c.6494A>G (p.Gln2165Arg)	rs200330029	0.00021
NM_002160.4(TNC):c.1822C>T (p.Arg608Cys)	rs138819573	0.00009
NM_002160.4(TNC):c.2239C>T (p.Arg747Trp)	rs776411890	0.00007
NM_002160.4(TNC):c.2960C>T (p.Thr987Met)	rs778506429	0.00007
NM_002160.4(TNC):c.2491G>A (p.Asp831Asn)	rs199896561	0.00004
NM_002160.4(TNC):c.1580G>C (p.Cys527Ser)	rs746843738	0.00001
NM_002160.4(TNC):c.1004G>C (p.Gly335Ala)
NM_002160.4(TNC):c.1622G>A (p.Arg541His)
NM_002160.4(TNC):c.2192A>C (p.Glu731Ala)
NM_002160.4(TNC):c.2434A>G (p.Lys812Glu)
NM_002160.4(TNC):c.2795G>C (p.Gly932Ala)	rs766474182
NM_002160.4(TNC):c.4490G>C (p.Gly1497Ala)
NM_002160.4(TNC):c.490C>G (p.Arg164Gly)	rs778273542
NM_002160.4(TNC):c.5692G>A (p.Val1898Ile)
NM_002160.4(TNC):c.6496-18del	rs1419724369
NM_002160.4(TNC):c.6527A>G (p.Glu2176Gly)
NM_002160.4(TNC):c.890A>G (p.Asn297Ser)	rs1554717312

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