ClinVar Miner

List of variants in gene TRIOBP reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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Gene type:
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Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_001039141.3(TRIOBP):c.5886A>G (p.Pro1962=) rs372220018 0.00171
NM_001039141.3(TRIOBP):c.3954C>T (p.Ser1318=) rs200990219 0.00157
NM_001039141.3(TRIOBP):c.4728T>C (p.Arg1576=) rs112874177 0.00143
NM_001039141.3(TRIOBP):c.6741G>A (p.Leu2247=) rs375013523 0.00137
NM_001039141.3(TRIOBP):c.4139A>G (p.Glu1380Gly) rs202059880 0.00133
NM_001039141.3(TRIOBP):c.5224C>T (p.Leu1742Phe) rs200493962 0.00129
NM_001039141.3(TRIOBP):c.5058C>G (p.Pro1686=) rs113459040 0.00123
NM_001039141.3(TRIOBP):c.4099C>T (p.Arg1367Trp) rs191589773 0.00097
NM_001039141.3(TRIOBP):c.363C>A (p.Ser121=) rs201843208 0.00091
NM_001039141.3(TRIOBP):c.202A>G (p.Thr68Ala) rs200529550 0.00063
NM_001039141.3(TRIOBP):c.5166C>G (p.Asp1722Glu) rs183189469 0.00061
NM_001039141.3(TRIOBP):c.6771G>A (p.Gln2257=) rs200793989 0.00058
NM_001039141.3(TRIOBP):c.4103G>A (p.Arg1368Gln) rs182816010 0.00040
NM_001039141.3(TRIOBP):c.6324+235C>T rs146823511 0.00040
NM_001039141.3(TRIOBP):c.4329A>G (p.Leu1443=) rs547759535 0.00035
NM_001039141.3(TRIOBP):c.4497T>G (p.Thr1499=) rs139919698 0.00034
NM_001039141.3(TRIOBP):c.4783C>T (p.Arg1595Cys) rs201117318 0.00034
NM_001039141.3(TRIOBP):c.6324+191G>A rs181741158 0.00031
NM_001039141.3(TRIOBP):c.6556G>A (p.Gly2186Ser) rs191901426 0.00031
NM_001039141.3(TRIOBP):c.5853G>A (p.Leu1951=) rs55821172 0.00030
NM_001039141.3(TRIOBP):c.483G>A (p.Glu161=) rs368119524 0.00028
NM_001039141.3(TRIOBP):c.6792G>A (p.Ser2264=) rs371118329 0.00026
NM_001039141.3(TRIOBP):c.6007G>A (p.Gly2003Ser) rs397516554 0.00021
NM_001039141.3(TRIOBP):c.4935A>G (p.Ala1645=) rs371078565 0.00020
NM_001039141.3(TRIOBP):c.409A>G (p.Ser137Gly) rs201008196 0.00017
NM_001039141.3(TRIOBP):c.4932C>T (p.Pro1644=) rs192500421 0.00016
NM_001039141.3(TRIOBP):c.6324+162G>A rs201529268 0.00016
NM_001039141.3(TRIOBP):c.6515G>A (p.Arg2172Gln) rs200528850 0.00013
NM_001039141.3(TRIOBP):c.6324+177G>A rs150061404 0.00009
NM_001039141.3(TRIOBP):c.5949C>T (p.Ser1983=) rs746538137 0.00006
NM_001039141.3(TRIOBP):c.6324+236G>A rs140572991 0.00006
NM_001039141.3(TRIOBP):c.6325-10C>T rs727503527 0.00006
NM_001039141.3(TRIOBP):c.7017C>T (p.Ile2339=) rs149496377 0.00005
NM_001039141.3(TRIOBP):c.*2+10G>A rs727503531 0.00004
NM_001039141.3(TRIOBP):c.477G>T (p.Arg159Ser) rs188030007 0.00004
NM_001039141.3(TRIOBP):c.7010G>A (p.Arg2337Gln) rs200850285 0.00004
NM_001039141.3(TRIOBP):c.5782A>G (p.Ile1928Val) rs781135139 0.00003
NM_001039141.3(TRIOBP):c.6039C>G (p.Pro2013=) rs876657596 0.00002
NM_001039141.3(TRIOBP):c.6324+194A>G rs727503526 0.00002
NM_001039141.3(TRIOBP):c.6575+14G>A rs577534147 0.00002
NM_001039141.3(TRIOBP):c.96C>T (p.Ala32=) rs563986808 0.00002
NM_001039141.3(TRIOBP):c.273A>G (p.Ala91=) rs876657592 0.00001
NM_001039141.3(TRIOBP):c.4135C>T (p.Pro1379Ser) rs727505118 0.00001
NM_001039141.3(TRIOBP):c.4429T>C (p.Trp1477Arg) rs756650521 0.00001
NM_001039141.3(TRIOBP):c.4548T>C (p.Pro1516=) rs770934306 0.00001
NM_001039141.3(TRIOBP):c.4773C>T (p.Ala1591=) rs876657594 0.00001
NM_001039141.3(TRIOBP):c.5247A>G (p.Ser1749=) rs1172498750 0.00001
NM_001039141.3(TRIOBP):c.6184A>G (p.Ser2062Gly) rs727503525 0.00001
NM_001039141.3(TRIOBP):c.6324+233C>G rs757097829 0.00001
NM_001039141.3(TRIOBP):c.6986G>A (p.Ser2329Asn) rs876657597 0.00001
NM_001039141.3(TRIOBP):c.301G>A (p.Ala101Thr) rs752612856
NM_001039141.3(TRIOBP):c.4101G>A (p.Arg1367=) rs727505244
NM_001039141.3(TRIOBP):c.4244G>A (p.Ser1415Asn) rs727505184
NM_001039141.3(TRIOBP):c.4271T>C (p.Leu1424Pro) rs727505298
NM_001039141.3(TRIOBP):c.4572G>A (p.Glu1524=) rs876657593
NM_001039141.3(TRIOBP):c.4621G>A (p.Ala1541Thr) rs727504784
NM_001039141.3(TRIOBP):c.4645C>T (p.Arg1549Cys) rs727505081
NM_001039141.3(TRIOBP):c.6283T>C (p.Ser2095Pro) rs369453731
NM_001039141.3(TRIOBP):c.6324+9G>A rs376601715
NM_001039141.3(TRIOBP):c.6936+13G>T rs727503529
NM_001039141.3(TRIOBP):c.6975T>C (p.Tyr2325=) rs1601672944

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