List of variants in gene combination TBCEL-TECTA, TECTA reported as likely benign for nonsyndromic genetic hearing loss

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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: 35

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HGVS	dbSNP	gnomAD frequency
NM_005422.4(TECTA):c.56A>G (p.Gln19Arg)	rs35507522	0.03926
NM_005422.4(TECTA):c.624+11C>G	rs73599492	0.03810
NM_005422.4(TECTA):c.5733T>G (p.Val1911=)	rs516678	0.03205
NM_005422.4(TECTA):c.3012C>G (p.Thr1004=)	rs61291716	0.02153
NM_005422.4(TECTA):c.4751G>C (p.Ser1584Thr)	rs34963131	0.02137
NM_005422.4(TECTA):c.5383+3G>A	rs73583199	0.01071
NM_005422.4(TECTA):c.-1-12T>C	rs145916279	0.00352
NM_005422.4(TECTA):c.701A>G (p.Gln234Arg)	rs144682235	0.00179
NM_005422.4(TECTA):c.2061C>G (p.Asn687Lys)	rs139165033	0.00171
NM_005422.4(TECTA):c.3097C>T (p.Arg1033Trp)	rs142486386	0.00149
NM_005422.4(TECTA):c.3492C>T (p.Thr1164=)	rs144012985	0.00138
NM_005422.4(TECTA):c.4720A>G (p.Ile1574Val)	rs147354818	0.00123
NM_005422.4(TECTA):c.1085G>T (p.Ser362Ile)	rs149001418	0.00104
NM_005422.4(TECTA):c.1002C>T (p.Asp334=)	rs35282525	0.00090
NM_005422.4(TECTA):c.2367+9C>T	rs368080945	0.00079
NM_005422.4(TECTA):c.4611C>T (p.Pro1537=)	rs138477419	0.00057
NM_005422.4(TECTA):c.1509C>T (p.Cys503=)	rs61733565	0.00050
NM_005422.4(TECTA):c.1291A>T (p.Thr431Ser)	rs138843691	0.00033
NM_005422.4(TECTA):c.5836T>C (p.Tyr1946His)	rs144343770	0.00032
NM_005422.4(TECTA):c.4315C>A (p.Leu1439Ile)	rs202199158	0.00026
NM_005422.4(TECTA):c.1461A>G (p.Gly487=)	rs202127508	0.00024
NM_005422.4(TECTA):c.3556C>T (p.Arg1186Trp)	rs148098950	0.00018
NM_005422.4(TECTA):c.5488G>A (p.Val1830Met)	rs189181502	0.00011
NM_005422.4(TECTA):c.4163G>A (p.Arg1388His)	rs150016625	0.00009
NM_005422.4(TECTA):c.65-14A>G	rs201171064	0.00009
NM_005422.4(TECTA):c.3511G>A (p.Val1171Met)	rs186780639	0.00008
NM_005422.4(TECTA):c.1621G>A (p.Val541Met)	rs370652301	0.00006
NM_005422.4(TECTA):c.1794G>C (p.Pro598=)	rs570667892	0.00003
NM_005422.4(TECTA):c.487-7C>G	rs368627411	0.00002
NM_005422.4(TECTA):c.5205C>T (p.Ala1735=)	rs762504147	0.00001
NM_005422.4(TECTA):c.5908G>A (p.Ala1970Thr)	rs202079138	0.00001
NM_005422.4(TECTA):c.805C>G (p.Arg269Gly)	rs777704329	0.00001
NM_005422.4(TECTA):c.29G>C (p.Trp10Ser)	rs1591433475
NM_005422.4(TECTA):c.4004G>A (p.Gly1335Glu)	rs148619105
NM_005422.4(TECTA):c.90A>T (p.Pro30=)	rs577470721

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