ClinVar Miner

List of variants in gene TRIP13 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 54
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HGVS dbSNP gnomAD frequency
NM_004237.4(TRIP13):c.259-54C>G rs7708206 0.17661
NM_004237.4(TRIP13):c.92+151C>G rs13181961 0.16633
NM_004237.4(TRIP13):c.608+39T>G rs12518024 0.14537
NM_004237.4(TRIP13):c.1133+244A>G rs56124764 0.09284
NM_004237.4(TRIP13):c.1204-216del rs56957846 0.09283
NM_004237.4(TRIP13):c.1133+243_1133+244insGT rs58555902 0.09282
NM_004237.4(TRIP13):c.609-151C>T rs45586233 0.08516
NM_004237.4(TRIP13):c.1134-61T>C rs56313889 0.08514
NM_004237.4(TRIP13):c.1134-112T>C rs56315432 0.08510
NM_004237.4(TRIP13):c.672+197G>A rs55900306 0.08499
NM_004237.4(TRIP13):c.1204-233T>G rs60132887 0.08470
NM_004237.4(TRIP13):c.445-33T>C rs6878334 0.08268
NC_000005.10:g.892840G>A rs113990338 0.07486
NM_004237.4(TRIP13):c.1204-13G>A rs58157086 0.06858
NM_004237.4(TRIP13):c.1204-17G>C rs58876062 0.05595
NM_004237.4(TRIP13):c.867-147G>A rs77084821 0.05588
NM_004237.4(TRIP13):c.444+216C>T rs73734002 0.05082
NM_004237.4(TRIP13):c.673-47C>T rs73734409 0.05074
NM_004237.4(TRIP13):c.259-123G>T rs7730877 0.05071
NM_004237.4(TRIP13):c.866+73T>C rs60113694 0.05071
NM_004237.4(TRIP13):c.444+175T>C rs72703173 0.04247
NM_004237.4(TRIP13):c.866+20A>G rs41283157 0.03441
NM_004237.4(TRIP13):c.1105T>C (p.Leu369=) rs35725571 0.03431
NM_004237.4(TRIP13):c.866+12A>G rs72703185 0.03428
NM_004237.4(TRIP13):c.1204-148G>A rs72703199 0.03427
NM_004237.4(TRIP13):c.1021-125G>A rs72703194 0.03424
NM_004237.4(TRIP13):c.444+250G>A rs60979695 0.02992
NM_004237.4(TRIP13):c.536-138C>T rs73020933 0.02991
NM_004237.4(TRIP13):c.673-168T>A rs73020941 0.02419
NM_004237.4(TRIP13):c.259-236C>T rs28672176 0.01989
NM_004237.4(TRIP13):c.535+7T>C rs80338980 0.00980
NM_004237.4(TRIP13):c.866+14G>A rs79236992 0.00503
NM_004237.4(TRIP13):c.277T>C (p.Cys93Arg) rs144634558 0.00313
NM_004237.4(TRIP13):c.1110C>T (p.Ser370=) rs145170850 0.00228
NM_004237.4(TRIP13):c.1020+19del rs148020919
NM_004237.4(TRIP13):c.1020+19dup
NM_004237.4(TRIP13):c.1021-20C>T
NM_004237.4(TRIP13):c.1021-271C>T rs72703193
NM_004237.4(TRIP13):c.1133+144GT[11] rs60208703
NM_004237.4(TRIP13):c.1133+144GT[12] rs60208703
NM_004237.4(TRIP13):c.1133+144GT[9] rs60208703
NM_004237.4(TRIP13):c.1204-216C>G rs1055758128
NM_004237.4(TRIP13):c.258+48del rs66843001
NM_004237.4(TRIP13):c.388+73_388+74insG rs369578570
NM_004237.4(TRIP13):c.388+74A>G rs920980
NM_004237.4(TRIP13):c.608+73del rs369501889
NM_004237.4(TRIP13):c.608+73dup rs369501889
NM_004237.4(TRIP13):c.732C>T (p.Asp244=)
NM_004237.4(TRIP13):c.759+17A>G
NM_004237.4(TRIP13):c.867-197_867-196insGAG rs61088975
NM_004237.4(TRIP13):c.906C>G (p.Thr302=) rs140779385
NM_004237.4(TRIP13):c.92+16C>G
NM_004237.4(TRIP13):c.92+16C>T
NM_004237.4(TRIP13):c.92+220C>G rs75110591

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