List of variants reported as benign for autosomal dominant nonsyndromic hearing loss 12 by Illumina Laboratory Services, Illumina

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Total variants: 29

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HGVS	dbSNP	gnomAD frequency
NM_005422.4(TECTA):c.5171G>A (p.Ser1724Asn)	rs526433	0.99235
NM_005422.4(TECTA):c.1485A>G (p.Ala495=)	rs536069	0.76077
NM_005422.4(TECTA):c.2805T>C (p.Tyr935=)	rs586473	0.73877
NM_005422.4(TECTA):c.1111A>G (p.Arg371Gly)	rs612969	0.48670
NM_005422.4(TECTA):c.4098G>A (p.Thr1366=)	rs12275038	0.28426
NM_005422.4(TECTA):c.4105+13C>T	rs7130952	0.26144
NM_005422.4(TECTA):c.2256C>T (p.Ile752=)	rs10502247	0.25910
NM_005422.4(TECTA):c.5634C>T (p.Ser1878=)	rs2155369	0.10906
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.4422C>T (p.Asn1474=)	rs33981325	0.02261
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.4533C>T (p.Phe1511=)	rs77628498	0.01098
NM_005422.4(TECTA):c.5383+3G>A	rs73583199	0.01071
NM_005422.4(TECTA):c.6250+4T>C	rs143302176	0.00811
NM_005422.4(TECTA):c.5012C>T (p.Ser1671Leu)	rs142948530	0.00672
NM_005422.4(TECTA):c.790+12C>T	rs138644808	0.00563
NM_005422.4(TECTA):c.2781T>C (p.His927=)	rs142903119	0.00395
NM_005422.4(TECTA):c.972G>C (p.Val324=)	rs147790742	0.00271
NM_005422.4(TECTA):c.1436C>T (p.Pro479Leu)	rs35107075	0.00186
NM_005422.4(TECTA):c.1651G>A (p.Val551Met)	rs200857366	0.00026
NM_005422.4(TECTA):c.4315C>A (p.Leu1439Ile)	rs202199158	0.00026
NM_005422.4(TECTA):c.4061C>T (p.Thr1354Ile)	rs148440178	0.00017
NM_005422.4(TECTA):c.6458C>T (p.Thr2153Met)	rs146965680	0.00007
NM_005422.4(TECTA):c.6428C>T (p.Ser2143Leu)	rs538443920	0.00004
NM_005422.4(TECTA):c.3750T>C (p.Asp1250=)	rs372087934	0.00003
NM_005422.4(TECTA):c.4295A>G (p.Lys1432Arg)	rs530918606	0.00002

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