ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 26
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001039141.3(TRIOBP):c.5014G>T (p.Gly1672Ter) rs200045032 0.00054
NM_001039141.3(TRIOBP):c.1039C>T (p.Arg347Ter) rs118204026 0.00010
NM_001039141.3(TRIOBP):c.3073C>T (p.Arg1025Ter) rs776962899 0.00006
NM_001039141.3(TRIOBP):c.3349C>T (p.Arg1117Ter) rs118204031 0.00003
NC_000022.10:g.(?_38111750)_(38111961_?)del
NM_001039141.3(TRIOBP):c.1195C>T (p.Arg399Ter) rs750078356
NM_001039141.3(TRIOBP):c.1222C>T (p.Gln408Ter) rs2145832569
NM_001039141.3(TRIOBP):c.1342del (p.Arg448fs)
NM_001039141.3(TRIOBP):c.1420C>T (p.Arg474Ter) rs1225633423
NM_001039141.3(TRIOBP):c.1960C>T (p.Arg654Ter)
NM_001039141.3(TRIOBP):c.2472del (p.Arg825fs)
NM_001039141.3(TRIOBP):c.251_254+22del rs1555894574
NM_001039141.3(TRIOBP):c.2548C>T (p.Gln850Ter)
NM_001039141.3(TRIOBP):c.2968C>T (p.Arg990Ter) rs1228392408
NM_001039141.3(TRIOBP):c.3214dup (p.Arg1072fs) rs1485334519
NM_001039141.3(TRIOBP):c.3295C>T (p.Gln1099Ter)
NM_001039141.3(TRIOBP):c.3460_3461del (p.Leu1154fs) rs771696726
NM_001039141.3(TRIOBP):c.3487_3533del (p.Pro1163fs) rs1569042640
NM_001039141.3(TRIOBP):c.3616_3617del (p.Leu1206fs)
NM_001039141.3(TRIOBP):c.3718del (p.Leu1240fs)
NM_001039141.3(TRIOBP):c.3854_3855del (p.Arg1285fs) rs750744696
NM_001039141.3(TRIOBP):c.4294G>T (p.Glu1432Ter)
NM_001039141.3(TRIOBP):c.4320_4321del (p.His1440fs)
NM_001039141.3(TRIOBP):c.4987dup (p.Gln1663fs)
NM_001039141.3(TRIOBP):c.5300_5301del (p.Leu1767fs)
NM_001039141.3(TRIOBP):c.6260del (p.Glu2087fs) rs2145871872

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.