ClinVar Miner

List of variants in gene TRIO reported as likely pathogenic for developmental disorder of mental health

Included ClinVar conditions (728):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_007118.4(TRIO):c.1665_1666delinsTT (p.Trp555_Gln556delinsCysTer) rs2152305937
NM_007118.4(TRIO):c.1863C>G (p.Tyr621Ter) rs140745100
NM_007118.4(TRIO):c.2302C>T (p.Gln768Ter) rs1554062562
NM_007118.4(TRIO):c.2570dup (p.Asn857fs) rs2152340697
NM_007118.4(TRIO):c.2638_2641dup (p.Leu881fs)
NM_007118.4(TRIO):c.298C>T (p.Arg100Ter)
NM_007118.4(TRIO):c.3224C>T (p.Thr1075Ile) rs1745368018
NM_007118.4(TRIO):c.3232C>T (p.Arg1078Trp)
NM_007118.4(TRIO):c.3570+3G>A rs2152354197
NM_007118.4(TRIO):c.3571C>T (p.Gln1191Ter)
NM_007118.4(TRIO):c.3657dup (p.Cys1220fs) rs1554068529
NM_007118.4(TRIO):c.3908C>T (p.Thr1303Ile) rs1746764895
NM_007118.4(TRIO):c.4085A>G (p.Tyr1362Cys)
NM_007118.4(TRIO):c.4103A>G (p.Asp1368Gly) rs2152363791
NM_007118.4(TRIO):c.4276G>T (p.Val1426Phe) rs1579522661
NM_007118.4(TRIO):c.4300C>T (p.Leu1434Phe) rs1747352673
NM_007118.4(TRIO):c.4382C>G (p.Pro1461Arg) rs1747667518
NM_007118.4(TRIO):c.4382C>T (p.Pro1461Leu) rs1747667518
NM_007118.4(TRIO):c.4387C>T (p.Arg1463Ter) rs748670822
NM_007118.4(TRIO):c.4394A>G (p.Asn1465Ser) rs1747669042
NM_007118.4(TRIO):c.4495del (p.Thr1499fs) rs2152373759
NM_007118.4(TRIO):c.4716G>A (p.Lys1572=)
NM_007118.4(TRIO):c.5619G>A (p.Met1873Ile)
NM_007118.4(TRIO):c.5680T>A (p.Leu1894Ile) rs2126522675
NM_007118.4(TRIO):c.5763+1G>T
NM_007118.4(TRIO):c.6092dup (p.Leu2031fs) rs752676391
NM_007118.4(TRIO):c.6153+1G>A rs1755124330
NM_007118.4(TRIO):c.651_652del (p.Arg217fs) rs1736840999
NM_007118.4(TRIO):c.6554_6557del (p.Glu2185fs) rs2126611738
NM_007118.4(TRIO):c.704del (p.Glu235fs) rs2152284932
NM_007118.4(TRIO):c.7050del (p.Val2351fs)
NM_007118.4(TRIO):c.7317_7345del (p.Ser2440fs)
NM_007118.4(TRIO):c.757dup (p.Ala253fs)
Single allele

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