ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 93
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HGVS dbSNP gnomAD frequency
NM_004239.4(TRIP11):c.139+291G>T rs2295174 0.79561
NM_004239.4(TRIP11):c.1314+162T>C rs2277526 0.65157
NM_004239.4(TRIP11):c.5719+314T>C rs2295162 0.52288
NM_004239.4(TRIP11):c.5160+195G>A rs8007661 0.52278
NM_004239.4(TRIP11):c.140-259C>T rs7143506 0.45546
NM_004239.4(TRIP11):c.1527+41A>G rs3818095 0.29544
NM_004239.4(TRIP11):c.4893-203G>A rs10134947 0.29498
NM_004239.4(TRIP11):c.5479G>A (p.Gly1827Ser) rs1051340 0.29281
NM_004239.4(TRIP11):c.4698+201G>A rs10147971 0.28838
NM_004239.4(TRIP11):c.5160+55G>T rs2273185 0.28788
NM_004239.4(TRIP11):c.5260+24T>C rs2273182 0.28783
NM_004239.4(TRIP11):c.5575-250G>A rs2295163 0.28228
NM_004239.2(TRIP11):c.-554A>G rs58339937 0.26808
NM_004239.4(TRIP11):c.140-251C>T rs7143499 0.25064
NM_004239.4(TRIP11):c.824-126T>G rs11160036 0.22814
NM_004239.4(TRIP11):c.589-133A>G rs11849778 0.22685
NM_004239.4(TRIP11):c.201+188A>C rs11621328 0.22495
NM_004239.4(TRIP11):c.1187-59T>C rs7151632 0.16634
NM_004239.4(TRIP11):c.1528-145T>C rs78426486 0.16634
NM_004239.4(TRIP11):c.4893-186G>A rs111429556 0.16545
NM_004239.4(TRIP11):c.658-311T>A rs17127862 0.16077
NM_004239.4(TRIP11):c.140-214G>A rs55707701 0.07542
NM_004239.4(TRIP11):c.5161-21T>A rs2273184 0.07452
NM_004239.4(TRIP11):c.115A>T (p.Met39Leu) rs17127898 0.06056
NM_004239.4(TRIP11):c.5574+86A>T rs71430745 0.05200
NM_004239.4(TRIP11):c.4892+238T>C rs10144861 0.05121
NM_004239.4(TRIP11):c.658-49A>G rs7158303 0.05100
NM_004239.4(TRIP11):c.4557+297T>C rs28459848 0.05083
NM_004239.4(TRIP11):c.5458-190G>A rs74071678 0.03841
NM_004239.4(TRIP11):c.5720-279A>G rs59369573 0.03832
NM_004239.4(TRIP11):c.5343-136A>G rs74071680 0.03715
NM_004239.4(TRIP11):c.1186+48T>G rs4530066 0.03707
NM_004239.4(TRIP11):c.823+111C>T rs28693952 0.03700
NM_004239.4(TRIP11):c.824-21T>G rs17127861 0.03696
NM_004239.4(TRIP11):c.4557+243T>G rs28703006 0.03680
NM_004239.4(TRIP11):c.4558-273A>G rs115544452 0.03001
NM_004239.4(TRIP11):c.*345T>C rs17127786 0.02579
NM_004239.4(TRIP11):c.4893-264G>T rs140838499 0.02567
NM_004239.4(TRIP11):c.4812T>C (p.Asp1604=) rs17127837 0.02457
NM_004239.4(TRIP11):c.5720-176A>G rs57710923 0.02429
NM_004239.4(TRIP11):c.5574+65C>G rs74071676 0.02427
NM_004239.4(TRIP11):c.5574+24T>C rs74071677 0.02424
NM_004239.4(TRIP11):c.202-96_202-95insT rs138279008 0.02385
NM_004239.4(TRIP11):c.5720-343C>T rs11160033 0.02166
NM_004239.4(TRIP11):c.823+30A>T rs79920810 0.02117
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.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.3147G>A (p.Leu1049=) rs17127842 0.00729
NM_004239.4(TRIP11):c.4164C>T (p.His1388=) rs140130380 0.00687
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.4413A>C (p.Thr1471=) rs144780536 0.00202
NM_004239.4(TRIP11):c.5246A>C (p.Glu1749Ala) rs2273183 0.00188
NM_004239.4(TRIP11):c.-61C>T rs78222479 0.00145
NM_004239.4(TRIP11):c.4139C>T (p.Thr1380Ile) rs117748213 0.00042
NM_004239.4(TRIP11):c.1187-218_1187-217del rs58527736
NM_004239.4(TRIP11):c.1227+246_1227+247dup rs200967942
NM_004239.4(TRIP11):c.1227+246dup rs200967942
NM_004239.4(TRIP11):c.1227+259_1227+271del rs200967942
NM_004239.4(TRIP11):c.1227+271del rs200967942
NM_004239.4(TRIP11):c.202-89A>G rs2295171
NM_004239.4(TRIP11):c.202-92_202-90dup rs771312948
NM_004239.4(TRIP11):c.4558-46GT[8] rs112793016
NM_004239.4(TRIP11):c.4893-105del rs34736578
NM_004239.4(TRIP11):c.5056+287_5056+289del rs145255981
NM_004239.4(TRIP11):c.5057-146G>A rs74073635
NM_004239.4(TRIP11):c.5160+230del rs11285699
NM_004239.4(TRIP11):c.5160+310dup rs59244424
NM_004239.4(TRIP11):c.5160+332del rs59244424
NM_004239.4(TRIP11):c.5342+193G>A rs11851669
NM_004239.4(TRIP11):c.5458-43del rs370006254
NM_004239.4(TRIP11):c.5458-55dup rs370006254
NM_004239.4(TRIP11):c.5574+85T>A rs76321048
NM_004239.4(TRIP11):c.5575-165del rs142203489
NM_004239.4(TRIP11):c.5575-182dup rs142203489
NM_004239.4(TRIP11):c.5720-70_5720-69insTATG rs3832961
NM_004239.4(TRIP11):c.588+166_588+167del rs35038594
NM_004239.4(TRIP11):c.588+167del rs35038594

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