List of variants in gene TMPRSS3 reported as benign for Autosomal recessive nonsyndromic hearing loss 8

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_001256317.3(TMPRSS3):c.447-13A>G	rs8130564	0.56900
NM_001256317.3(TMPRSS3):c.453G>A (p.Val151=)	rs2839501	0.49190
NM_001256317.3(TMPRSS3):c.*206A>G	rs225309	0.35946
NM_001256317.3(TMPRSS3):c.*2G>A	rs13047838	0.17560
NM_001256317.3(TMPRSS3):c.757A>G (p.Ile253Val)	rs2839500	0.16545
NM_001256317.3(TMPRSS3):c.331G>A (p.Gly111Ser)	rs35227181	0.12359
NM_001256317.3(TMPRSS3):c.157G>A (p.Val53Ile)	rs928302	0.08425
NM_001256317.3(TMPRSS3):c.268G>A (p.Ala90Thr)	rs45598239	0.03352
NM_001256317.3(TMPRSS3):c.-51-7G>C	rs4920100	0.02415
NM_001256317.3(TMPRSS3):c.432A>G (p.Gln144=)	rs61731564	0.02161
NM_001256317.3(TMPRSS3):c.952+17A>G	rs115489719	0.01047
NM_001256317.3(TMPRSS3):c.617-18C>T	rs225431	0.00940
NM_001256317.3(TMPRSS3):c.933C>T (p.Ala311=)	rs145235893	0.00153
NM_001256317.3(TMPRSS3):c.231C>T (p.Tyr77=)	rs139934512	0.00125
NM_024022.2(TMPRSS3):c.617-3_617-2dup	rs34966432

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