List of variants in gene TCTN3 reported 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
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_015631.6(TCTN3):c.603T>A (p.Thr201=)	rs10786229	0.35079
NM_015631.6(TCTN3):c.500-11A>T	rs11188434	0.18618
NM_015631.6(TCTN3):c.925G>T (p.Ala309Ser)	rs55859130	0.01420
NM_015631.6(TCTN3):c.630T>C (p.Ala210=)	rs41299157	0.00543
NM_015631.6(TCTN3):c.1030G>A (p.Gly344Arg)	rs141088838	0.00423
NM_015631.6(TCTN3):c.946A>G (p.Thr316Ala)	rs200042949	0.00118
NM_015631.6(TCTN3):c.1764C>T (p.Val588=)	rs137856303	0.00071
NM_015631.6(TCTN3):c.280T>C (p.Leu94=)	rs367982164	0.00062
NM_015631.6(TCTN3):c.1096-14C>A	rs41291568	0.00022
NM_015631.6(TCTN3):c.1537C>T (p.Pro513Ser)	rs755942179	0.00004
NM_015631.6(TCTN3):c.627+1G>A	rs1566074908	0.00001
NM_015631.6(TCTN3):c.1029G>A (p.Leu343=)
NM_015631.6(TCTN3):c.380+10G>C
NM_015631.6(TCTN3):c.628-10T>C
NM_015631.6(TCTN3):c.737-16A>T	rs886038621

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