List of variants in gene TRIO reported as benign by Invitae

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: 35

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HGVS	dbSNP	gnomAD frequency
NM_007118.4(TRIO):c.3571-4G>A	rs16903450	0.01703
NM_007118.4(TRIO):c.5763+6G>T	rs73749263	0.00916
NM_007118.4(TRIO):c.171C>T (p.Asn57=)	rs55664610	0.00913
NM_007118.4(TRIO):c.7457_7468del (p.Trp2486_Pro2490delinsSer)	rs140308852	0.00802
NM_007118.4(TRIO):c.7391C>T (p.Ala2464Val)	rs115054458	0.00760
NM_007118.4(TRIO):c.347+3A>G	rs16903358	0.00665
NM_007118.4(TRIO):c.4837G>A (p.Ala1613Thr)	rs16903474	0.00590
NM_007118.4(TRIO):c.2811C>G (p.Ala937=)	rs143042118	0.00529
NM_007118.4(TRIO):c.7115C>T (p.Pro2372Leu)	rs199631028	0.00488
NM_007118.4(TRIO):c.8447A>G (p.Lys2816Arg)	rs73749289	0.00475
NM_007118.4(TRIO):c.1179C>T (p.Asn393=)	rs56035446	0.00399
NM_007118.4(TRIO):c.7367C>T (p.Pro2456Leu)	rs75338052	0.00326
NM_007118.4(TRIO):c.8831A>G (p.Asn2944Ser)	rs143213427	0.00279
NM_007118.4(TRIO):c.9247C>T (p.Arg3083Cys)	rs61740945	0.00272
NM_007118.4(TRIO):c.6888C>T (p.Gly2296=)	rs200735300	0.00234
NM_007118.4(TRIO):c.2928G>A (p.Gln976=)	rs148506244	0.00208
NM_007118.4(TRIO):c.9110A>T (p.Lys3037Met)	rs55900671	0.00179
NM_007118.4(TRIO):c.34G>A (p.Ala12Thr)	rs1045136451	0.00141
NM_007118.4(TRIO):c.3639T>C (p.His1213=)	rs140850570	0.00122
NM_007118.4(TRIO):c.2889C>T (p.Ser963=)	rs10064745	0.00113
NM_007118.4(TRIO):c.558A>G (p.Leu186=)	rs141383076	0.00081
NM_007118.4(TRIO):c.3276C>T (p.Ser1092=)	rs145133665	0.00069
NM_007118.4(TRIO):c.7401T>C (p.Ser2467=)	rs377647192	0.00046
NM_007118.4(TRIO):c.1054-7C>T	rs4702026	0.00044
NM_007118.4(TRIO):c.7800C>T (p.Pro2600=)	rs147014315	0.00019
NM_007118.4(TRIO):c.2480G>A (p.Arg827His)	rs370634993	0.00016
NM_007118.4(TRIO):c.2583C>T (p.Ala861=)	rs191608099	0.00009
NM_007118.4(TRIO):c.1209G>A (p.Ser403=)	rs189300218	0.00006
NM_007118.4(TRIO):c.6654C>A (p.Ile2218=)	rs201985481	0.00006
NM_007118.4(TRIO):c.3067-4A>T	rs200412925	0.00005
NM_007118.4(TRIO):c.2588-9T>C	rs377210006	0.00004
NM_007118.4(TRIO):c.8919G>A (p.Ser2973=)	rs564650565	0.00004
NM_007118.4(TRIO):c.3067-10C>T	rs375115645	0.00001
NM_007118.4(TRIO):c.6725C>T (p.Thr2242Met)	rs55916212	0.00001
NM_007118.4(TRIO):c.6877GGC[7] (p.Gly2298dup)	rs749785358

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