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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 38

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HGVS	dbSNP	gnomAD frequency
NM_001039141.3(TRIOBP):c.5705A>C (p.Lys1902Thr)	rs138804394	0.00071
NM_001039141.3(TRIOBP):c.5014G>T (p.Gly1672Ter)	rs200045032	0.00054
NM_001039141.3(TRIOBP):c.4666G>A (p.Glu1556Lys)	rs376793698	0.00042
NM_001039141.3(TRIOBP):c.6803G>A (p.Gly2268Asp)	rs200411253	0.00019
NM_001039141.3(TRIOBP):c.5788C>T (p.Arg1930Trp)	rs142769400	0.00017
NM_001039141.3(TRIOBP):c.5167C>A (p.Gln1723Lys)	rs370224413	0.00013
NM_001039141.3(TRIOBP):c.6775C>T (p.Arg2259Cys)	rs536411182	0.00012
NM_001039141.3(TRIOBP):c.6961T>C (p.Tyr2321His)	rs727503530	0.00009
NM_001039141.3(TRIOBP):c.5266C>T (p.Arg1756Trp)	rs774610362	0.00006
NM_001039141.3(TRIOBP):c.6248G>A (p.Arg2083His)	rs185791823	0.00006
NM_001039141.3(TRIOBP):c.6776G>A (p.Arg2259His)	rs554837585	0.00005
NM_001039141.3(TRIOBP):c.5198C>T (p.Pro1733Leu)	rs373745908	0.00004
NM_001039141.3(TRIOBP):c.6196G>A (p.Glu2066Lys)	rs564506970	0.00004
NM_001039141.3(TRIOBP):c.6308C>T (p.Pro2103Leu)	rs200250028	0.00004
NM_001039141.3(TRIOBP):c.6170G>A (p.Arg2057His)	rs377068258	0.00003
NM_001039141.3(TRIOBP):c.6830G>A (p.Arg2277Gln)	rs775565659	0.00003
NM_001039141.3(TRIOBP):c.5891G>A (p.Arg1964His)	rs534138620	0.00002
NM_001039141.3(TRIOBP):c.5929C>T (p.Arg1977Trp)	rs367584370	0.00002
NM_001039141.3(TRIOBP):c.64C>T (p.Arg22Cys)	rs374228600	0.00002
NM_001039141.3(TRIOBP):c.-3A>G	rs779160270	0.00001
NM_001039141.3(TRIOBP):c.115-12A>T	rs781452420	0.00001
NM_001039141.3(TRIOBP):c.4009C>G (p.Gln1337Glu)	rs372970338	0.00001
NM_001039141.3(TRIOBP):c.4062+5G>A	rs876658037	0.00001
NM_001039141.3(TRIOBP):c.5185-12C>G	rs774556951	0.00001
NM_001039141.3(TRIOBP):c.5693C>T (p.Ser1898Leu)	rs727503523	0.00001
NM_001039141.3(TRIOBP):c.5869C>T (p.Gln1957Ter)	rs1277466514	0.00001
NM_001039141.3(TRIOBP):c.6324+240G>A	rs876658038	0.00001
NC_000022.11:g.(?_37738534)_(37741122_?)del
NM_001039141.3(TRIOBP):c.111C>G (p.Tyr37Ter)	rs876658035
NM_001039141.3(TRIOBP):c.202A>T (p.Thr68Ser)	rs200529550
NM_001039141.3(TRIOBP):c.3948G>A (p.Arg1316=)	rs876658036
NM_001039141.3(TRIOBP):c.4703C>G (p.Ala1568Gly)	rs569914227
NM_001039141.3(TRIOBP):c.5117A>G (p.Glu1706Gly)	rs727503522
NM_001039141.3(TRIOBP):c.5193G>C (p.Lys1731Asn)	rs1207596715
NM_001039141.3(TRIOBP):c.5890C>G (p.Arg1964Gly)	rs565618931
NM_001039141.3(TRIOBP):c.5936T>C (p.Leu1979Pro)	rs727503524
NM_001039141.3(TRIOBP):c.6205G>A (p.Glu2069Lys)	rs777449279
NM_001039141.3(TRIOBP):c.6324+214G>A	rs1601661052

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