List of variants in gene combination TBCEL-TECTA, TECTA reported as benign by PreventionGenetics, part of Exact Sciences

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: 16

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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.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.4422C>T (p.Asn1474=)	rs33981325	0.02261
NM_005422.4(TECTA):c.5012C>T (p.Ser1671Leu)	rs142948530	0.00672
NM_005422.4(TECTA):c.5384-19G>A	rs7111480	0.00609
NM_005422.4(TECTA):c.790+12C>T	rs138644808	0.00563
NM_005422.4(TECTA):c.-1-12T>C	rs145916279	0.00352
NM_005422.4(TECTA):c.3304G>A (p.Val1102Ile)	rs34658230	0.00253
NM_005422.4(TECTA):c.1436C>T (p.Pro479Leu)	rs35107075	0.00186

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