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

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

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.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.628+2T>C
NM_001039141.3(TRIOBP):c.6849+1G>T	rs2145882160

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