List of variants in gene TRIOBP reported as benign for auditory system disorder

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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: 20

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HGVS	dbSNP	gnomAD frequency
NM_001039141.3(TRIOBP):c.6324+46C>G	rs5756810	0.96820
NM_001039141.3(TRIOBP):c.4129T>C (p.Trp1377Arg)	rs8140958	0.96815
NM_001039141.3(TRIOBP):c.3899A>G (p.His1300Arg)	rs739138	0.58971
NM_001039141.3(TRIOBP):c.4063-21A>C	rs13054052	0.54357
NM_001039141.3(TRIOBP):c.650G>A (p.Ser217Asn)	rs12628603	0.54098
NM_001039141.3(TRIOBP):c.3975G>A (p.Gln1325=)	rs7284476	0.35508
NM_001039141.3(TRIOBP):c.3885C>T (p.Ser1295=)	rs739137	0.35439
NM_001039141.3(TRIOBP):c.2589C>A (p.Asn863Lys)	rs9610841	0.35396
NM_001039141.3(TRIOBP):c.3559T>C (p.Phe1187Leu)	rs5756795	0.35350
NM_001039141.3(TRIOBP):c.-14C>G	rs12484441	0.18268
NM_001039141.3(TRIOBP):c.2477C>T (p.Ser826Leu)	rs41296243	0.01649
NM_001039141.3(TRIOBP):c.3089C>G (p.Pro1030Arg)	rs193043234	0.00922
NM_001039141.3(TRIOBP):c.*3-4T>C	rs145222008	0.00848
NM_001039141.3(TRIOBP):c.6741G>A (p.Leu2247=)	rs375013523	0.00137
NM_001039141.3(TRIOBP):c.634G>A (p.Gly212Ser)	rs201794404	0.00115
NM_001039141.3(TRIOBP):c.2201C>T (p.Ser734Phe)	rs199794705	0.00069
NM_001039141.3(TRIOBP):c.4077T>C (p.Pro1359=)	rs139074745	0.00058
NM_001039141.3(TRIOBP):c.1193_1195del (p.Gln398del)	rs55745992
NM_001039141.3(TRIOBP):c.1478G>A (p.Ser493Asn)	rs4821700
NM_001039141.3(TRIOBP):c.6472+19dup	rs3833924

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