List of variants in gene TRIP11 reported as benign for not specified

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: 26

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_004239.4(TRIP11):c.5479G>A (p.Gly1827Ser)	rs1051340	0.29281
NM_004239.4(TRIP11):c.115A>T (p.Met39Leu)	rs17127898	0.06056
NM_004239.4(TRIP11):c.5255G>A (p.Arg1752Lys)	rs11851376	0.03105
NM_004239.4(TRIP11):c.4812T>C (p.Asp1604=)	rs17127837	0.02457
NM_004239.4(TRIP11):c.405T>C (p.Ala135=)	rs77981249	0.01569
NM_004239.4(TRIP11):c.5781G>A (p.Ser1927=)	rs3742719	0.01567
NM_004239.4(TRIP11):c.4727G>A (p.Arg1576His)	rs35007347	0.01467
NM_004239.4(TRIP11):c.2651A>G (p.Asp884Gly)	rs34967261	0.01405
NM_004239.4(TRIP11):c.3306T>C (p.Phe1102=)	rs34151071	0.01402
NM_004239.4(TRIP11):c.1527+6A>G	rs17127844	0.01376
NM_004239.4(TRIP11):c.2931C>T (p.Thr977=)	rs7152887	0.01366
NM_004239.4(TRIP11):c.2383G>C (p.Val795Leu)	rs34699762	0.01322
NM_004239.4(TRIP11):c.202-7T>A	rs56034853	0.01303
NM_004239.4(TRIP11):c.3118A>G (p.Ile1040Val)	rs34805848	0.01111
NM_004239.4(TRIP11):c.3714G>A (p.Glu1238=)	rs34919898	0.01101
NM_004239.4(TRIP11):c.5160+59A>G	rs117502191	0.00901
NM_004239.4(TRIP11):c.5651A>G (p.His1884Arg)	rs74071672	0.00895
NM_004239.4(TRIP11):c.2134G>A (p.Glu712Lys)	rs143524436	0.00835
NM_004239.4(TRIP11):c.1517A>C (p.Glu506Ala)	rs2273186	0.00816
NM_004239.4(TRIP11):c.4507A>G (p.Met1503Val)	rs34839498	0.00686
NM_004239.4(TRIP11):c.2217T>C (p.Tyr739=)	rs35009380	0.00682
NM_004239.4(TRIP11):c.3858G>A (p.Gln1286=)	rs35798420	0.00558
NM_004239.4(TRIP11):c.1904C>G (p.Ser635Cys)	rs59635749	0.00410
NM_004239.4(TRIP11):c.5086G>A (p.Glu1696Lys)	rs80200454	0.00410
NM_004239.4(TRIP11):c.5246A>C (p.Glu1749Ala)	rs2273183	0.00188
NM_004239.4(TRIP11):c.4139C>T (p.Thr1380Ile)	rs117748213	0.00042

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.