ClinVar Miner

List of variants in gene TRIOBP reported as likely pathogenic for not provided

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Total variants: 17
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HGVS dbSNP gnomAD frequency
NM_001039141.3(TRIOBP):c.5014G>T (p.Gly1672Ter) rs200045032 0.00054
NM_001039141.3(TRIOBP):c.1933C>T (p.Gln645Ter) rs377748152 0.00016
NM_001039141.3(TRIOBP):c.163C>T (p.Arg55Ter) rs369119867 0.00011
NM_001039141.3(TRIOBP):c.3073C>T (p.Arg1025Ter) rs776962899 0.00006
NM_001039141.3(TRIOBP):c.629-1G>C rs766809690 0.00005
NM_001039141.3(TRIOBP):c.5184+1G>A rs575123401 0.00004
NM_001039141.3(TRIOBP):c.4130G>A (p.Trp1377Ter) rs747619979 0.00001
NM_001039141.3(TRIOBP):c.1866_1867del (p.Asp622fs) rs2145833327
NM_001039141.3(TRIOBP):c.2609_2619del (p.Gln870fs) rs1180979609
NM_001039141.3(TRIOBP):c.3854_3855del (p.Arg1285fs) rs750744696
NM_001039141.3(TRIOBP):c.4062+2T>C rs1057520081
NM_001039141.3(TRIOBP):c.4232_4233del (p.Arg1411fs) rs1233777224
NM_001039141.3(TRIOBP):c.4436dup (p.Thr1480fs)
NM_001039141.3(TRIOBP):c.4526_4527del (p.Arg1509fs) rs1601639680
NM_001039141.3(TRIOBP):c.5233C>T (p.Arg1745Ter)
NM_001039141.3(TRIOBP):c.5305del (p.Val1769fs)
NM_001039141.3(TRIOBP):c.6849+1G>T rs2145882160

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