List of variants in gene TCTN1 reported as likely 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: 19

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HGVS	dbSNP	gnomAD frequency
NM_001082538.3(TCTN1):c.1387T>C (p.Trp463Arg)	rs114568905	0.00194
NM_001082538.3(TCTN1):c.1471A>T (p.Ile491Phe)	rs201894544	0.00146
NM_001082538.3(TCTN1):c.1410C>T (p.Tyr470=)	rs370336923	0.00108
NM_001082538.3(TCTN1):c.298G>A (p.Val100Met)	rs145478892	0.00073
NM_001082538.3(TCTN1):c.960C>T (p.Cys320=)	rs145970332	0.00051
NM_001082538.3(TCTN1):c.1563C>T (p.Tyr521=)	rs368907353	0.00048
NM_001082538.3(TCTN1):c.1671C>A (p.Ser557=)	rs200067409	0.00014
NM_001082538.3(TCTN1):c.-19C>A	rs773061089	0.00005
NM_001082538.3(TCTN1):c.285C>T (p.Pro95=)	rs199664343	0.00005
NM_001082538.3(TCTN1):c.1149C>T (p.Val383=)	rs759588884	0.00002
NM_001082538.3(TCTN1):c.954C>T (p.Ser318=)	rs372535670	0.00002
NM_001082538.3(TCTN1):c.1659G>A (p.Thr553=)	rs777278093	0.00001
NM_001082538.3(TCTN1):c.-8C>T	rs886038410
NM_001082538.3(TCTN1):c.341+10C>T	rs201488724
NM_001082538.3(TCTN1):c.473-10del	rs771463400
NM_001082538.3(TCTN1):c.483A>T (p.Ala161=)
NM_001082538.3(TCTN1):c.624+122A>G
NM_001082538.3(TCTN1):c.699TAA[1] (p.Asn235del)	rs797046038
NM_001082538.3(TCTN1):c.713-227G>A

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