"PreventionGenetics, part of Exact Sciences"[submitter] AND "TRIP13"[g - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3031748	NM_004237.4(TRIP13):c.51G>A (p.Glu17=)	TRIP13	Single nucleotide variant (synonymous variant)	TRIP13-related disorder	GLikely benign
Select item 2817509	NM_004237.4(TRIP13):c.92+6C>G	TRIP13	Single nucleotide variant (intron variant)	TRIP13-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 747571	NM_004237.4(TRIP13):c.123T>C (p.Ser41=)	TRIP13	Single nucleotide variant (synonymous variant)	TRIP13-related disorder +1 more	GLikely benign
Select item 726741	NM_004237.4(TRIP13):c.277T>C (p.Cys93Arg)	TRIP13 (C93R)	Single nucleotide variant (missense variant)	TRIP13-related disorder +1 more	GBenign
Select item 3061491	NM_004237.4(TRIP13):c.423C>T (p.Tyr141=)	TRIP13	Single nucleotide variant (synonymous variant)	TRIP13-related disorder	GLikely benign
Select item 3045121	NM_004237.4(TRIP13):c.445-5A>G	TRIP13	Single nucleotide variant (intron variant)	TRIP13-related disorder	GLikely benign
Select item 725450	NM_004237.4(TRIP13):c.516C>T (p.Asn172=)	TRIP13	Single nucleotide variant (synonymous variant)	TRIP13-related disorder +1 more	GLikely benign
Select item 3058099	NM_004237.4(TRIP13):c.608+10G>A	TRIP13	Single nucleotide variant (intron variant)	TRIP13-related disorder	GLikely benign
Select item 790007	NM_004237.4(TRIP13):c.614G>A (p.Arg205Gln)	TRIP13 (R205Q)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 2722543	NM_004237.4(TRIP13):c.732C>T (p.Asp244=)	TRIP13	Single nucleotide variant (synonymous variant)	TRIP13-related disorder +1 more	GBenign/Likely benign
Select item 3039276	NM_004237.4(TRIP13):c.778G>A (p.Ala260Thr)	TRIP13 (A260T)	Single nucleotide variant (missense variant)	TRIP13-related disorder	GUncertain significance
Select item 3049309	NM_004237.4(TRIP13):c.825C>T (p.Arg275=)	TRIP13	Single nucleotide variant (synonymous variant)	TRIP13-related disorder	GLikely benign
Select item 3030857	NM_004237.4(TRIP13):c.906C>T (p.Thr302=)	TRIP13	Single nucleotide variant (synonymous variant)	TRIP13-related disorder	GLikely benign
Select item 2636923	NM_004237.4(TRIP13):c.988A>G (p.Ile330Val)	TRIP13 (I330V)	Single nucleotide variant (missense variant)	TRIP13-related disorder	GUncertain significance
Select item 722937	NM_004237.4(TRIP13):c.1110C>T (p.Ser370=)	TRIP13	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 2636088	NM_004237.4(TRIP13):c.1136A>G (p.Lys379Arg)	TRIP13 (K379R)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3054360	NM_004237.4(TRIP13):c.1257C>T (p.Asp419=)	TRIP13	Single nucleotide variant (synonymous variant)	TRIP13-related disorder	GLikely benign
Select item 2898842	NM_004237.4(TRIP13):c.1272G>A (p.Glu424=)	TRIP13	Single nucleotide variant (synonymous variant)	TRIP13-related disorder +1 more	GLikely benign
Select item 735470	NM_004237.4(TRIP13):c.1294A>G (p.Ile432Val)	TRIP13 (I432V)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign