List of variants in gene TCTN3 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_015631.6(TCTN3):c.630T>C (p.Ala210=)	rs41299157	0.00543
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.1425G>A (p.Arg475=)	rs144543830	0.00065
NM_015631.6(TCTN3):c.324C>T (p.Asp108=)	rs566756038	0.00001
NM_015631.6(TCTN3):c.606A>G (p.Gln202=)	rs777642622	0.00001
NM_015631.6(TCTN3):c.1203+69T>C
NM_015631.6(TCTN3):c.1792C>T (p.Leu598=)
NM_015631.6(TCTN3):c.770G>A (p.Arg257His)	rs758733887

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