List of variants in gene combination TBCEL-TECTA, TECTA reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_005422.4(TECTA):c.5012C>T (p.Ser1671Leu)	rs142948530	0.00672
NM_005422.4(TECTA):c.2061C>G (p.Asn687Lys)	rs139165033	0.00171
NM_005422.4(TECTA):c.4633G>A (p.Val1545Ile)	rs377156351	0.00024
NM_005422.4(TECTA):c.33C>A (p.Val11=)	rs140393508	0.00015
NM_005422.4(TECTA):c.4824C>T (p.Ile1608=)	rs747713348	0.00011
NM_005422.4(TECTA):c.915C>T (p.Cys305=)	rs367974065	0.00011
NM_005422.4(TECTA):c.2184C>T (p.Ser728=)	rs148638616	0.00007
NM_005422.4(TECTA):c.6401C>T (p.Thr2134Met)	rs372282487	0.00006
NM_005422.4(TECTA):c.3750T>C (p.Asp1250=)	rs372087934	0.00003
NM_005422.4(TECTA):c.1503C>T (p.Ser501=)
NM_005422.4(TECTA):c.3250A>G (p.Met1084Val)
NM_005422.4(TECTA):c.6402G>A (p.Thr2134=)	rs141203939
NM_005422.4(TECTA):c.837C>T (p.Cys279=)	rs1946520391

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