| 597799089 | CV3623140 | single nucleotide variant | NM_153210.5(USP43):c.23C>G (p.Ala8Gly) | not specified [RCV004879486] | uncertain significance | 17 | 9645655 | 9645655 | Human | | name |
| 156340223 | CV2229441 | single nucleotide variant | NM_153210.5(USP43):c.38C>A (p.Pro13Gln) | not specified [RCV004101213] | uncertain significance | 17 | 9645670 | 9645670 | Human | | name |
| 156213201 | CV2257354 | single nucleotide variant | NM_153210.5(USP43):c.88C>T (p.Arg30Cys) | not specified [RCV004125446] | uncertain significance | 17 | 9645720 | 9645720 | Human | | name |
| 155928973 | CV2363403 | single nucleotide variant | NM_153210.5(USP43):c.88C>G (p.Arg30Gly) | not specified [RCV004215987] | uncertain significance | 17 | 9645720 | 9645720 | Human | | name |
| 405800868 | CV3338321 | single nucleotide variant | NM_153210.5(USP43):c.58C>G (p.Arg20Gly) | not specified [RCV004477520] | uncertain significance | 17 | 9645690 | 9645690 | Human | | name |
| 405800978 | CV3338323 | single nucleotide variant | NM_153210.5(USP43):c.62G>C (p.Arg21Pro) | not specified [RCV004477522] | uncertain significance | 17 | 9645694 | 9645694 | Human | | name |
| 407528932 | CV3487671 | single nucleotide variant | NM_153210.5(USP43):c.52C>T (p.Pro18Ser) | not specified [RCV004680639] | uncertain significance | 17 | 9645684 | 9645684 | Human | | name |
| 407528934 | CV3487672 | single nucleotide variant | NM_153210.5(USP43):c.38C>T (p.Pro13Leu) | not specified [RCV004680640] | uncertain significance | 17 | 9645670 | 9645670 | Human | | name |
| 597799217 | CV3623128 | single nucleotide variant | NM_153210.5(USP43):c.56G>A (p.Arg19His) | not specified [RCV004879478] | uncertain significance | 17 | 9645688 | 9645688 | Human | | name |
| 597696710 | CV3623143 | single nucleotide variant | NM_153210.5(USP43):c.56G>T (p.Arg19Leu) | not specified [RCV004885186] | uncertain significance | 17 | 9645688 | 9645688 | Human | | name |
| 156221071 | CV2222451 | single nucleotide variant | NM_153210.5(USP43):c.178G>A (p.Gly60Ser) | not specified [RCV004099305] | uncertain significance | 17 | 9645810 | 9645810 | Human | | name |
| 156068588 | CV2320449 | single nucleotide variant | NM_153210.5(USP43):c.112C>G (p.Arg38Gly) | not specified [RCV004172091] | uncertain significance | 17 | 9645744 | 9645744 | Human | | name |
| 156347433 | CV2375452 | single nucleotide variant | NM_153210.5(USP43):c.101C>A (p.Ala34Glu) | not specified [RCV004225966] | uncertain significance | 17 | 9645733 | 9645733 | Human | | name |
| 329369410 | CV2450634 | single nucleotide variant | NM_153210.5(USP43):c.124G>A (p.Gly42Arg) | not specified [RCV004265525] | uncertain significance | 17 | 9645756 | 9645756 | Human | | name |
| 401861632 | CV2756385 | single nucleotide variant | NM_153210.5(USP43):c.236G>A (p.Arg79His) | not specified [RCV004342927] | uncertain significance | 17 | 9645868 | 9645868 | Human | | name |
| 401935689 | CV2814943 | single nucleotide variant | NM_153210.5(USP43):c.2106T>G (p.Ala702=) | not provided [RCV003413149] | likely benign | 17 | 9710050 | 9710050 | Human | | name |
| 405800854 | CV3338313 | single nucleotide variant | NM_153210.5(USP43):c.284C>T (p.Ala95Val) | not specified [RCV004477512] | uncertain significance | 17 | 9645916 | 9645916 | Human | | name |
| 597799227 | CV3623122 | single nucleotide variant | NM_153210.5(USP43):c.248C>A (p.Pro83His) | not specified [RCV004879473] | uncertain significance | 17 | 9645880 | 9645880 | Human | | name |
| 597799140 | CV3623139 | single nucleotide variant | NM_153210.5(USP43):c.156C>A (p.His52Gln) | not specified [RCV004879485] | uncertain significance | 17 | 9645788 | 9645788 | Human | | name |
| 15201190 | CV704531 | single nucleotide variant | NM_153210.5(USP43):c.1350A>T (p.Val450=) | not provided [RCV000957551] | benign | 17 | 9686906 | 9686906 | Human | | name |
| 15198281 | CV727625 | single nucleotide variant | NM_153210.5(USP43):c.2487C>T (p.Ser829=) | not provided [RCV000890311] | benign | 17 | 9728105 | 9728105 | Human | | name |
| 156385832 | CV2228045 | single nucleotide variant | NM_153210.5(USP43):c.814A>G (p.Ile272Val) | not specified [RCV004096284] | uncertain significance | 17 | 9674964 | 9674964 | Human | | name |
| 155992651 | CV2255859 | single nucleotide variant | NM_153210.5(USP43):c.541A>G (p.Asn181Asp) | not specified [RCV004122017] | uncertain significance | 17 | 9656439 | 9656439 | Human | | name |
| 156184528 | CV2294881 | single nucleotide variant | NM_153210.5(USP43):c.438G>T (p.Gln146His) | not specified [RCV004156037] | uncertain significance | 17 | 9646070 | 9646070 | Human | | name |
| 156274063 | CV2320230 | single nucleotide variant | NM_153210.5(USP43):c.932A>G (p.Lys311Arg) | not specified [RCV004169849] | likely benign | 17 | 9676844 | 9676844 | Human | | name |
| 156294423 | CV2336771 | single nucleotide variant | NM_153210.5(USP43):c.734A>T (p.Gln245Leu) | not specified [RCV004197007] | uncertain significance | 17 | 9666745 | 9666745 | Human | | name |
| 401748696 | CV2692714 | single nucleotide variant | NM_153210.5(USP43):c.410C>T (p.Ala137Val) | not specified [RCV004306266] | uncertain significance | 17 | 9646042 | 9646042 | Human | | name |
| 401767316 | CV2727007 | single nucleotide variant | NM_153210.5(USP43):c.995G>T (p.Ser332Ile) | not specified [RCV004325389] | uncertain significance | 17 | 9680256 | 9680256 | Human | | name |
| 405800867 | CV3338320 | single nucleotide variant | NM_153210.5(USP43):c.499T>C (p.Phe167Leu) | not specified [RCV004477519] | uncertain significance | 17 | 9646131 | 9646131 | Human | | name |
| 405800870 | CV3338322 | single nucleotide variant | NM_153210.5(USP43):c.607G>A (p.Gly203Ser) | not specified [RCV004477521] | uncertain significance | 17 | 9656505 | 9656505 | Human | | name |
| 405800874 | CV3338324 | single nucleotide variant | NM_153210.5(USP43):c.955G>A (p.Val319Ile) | not specified [RCV004477523] | likely benign | 17 | 9676867 | 9676867 | Human | | name |
| 597799045 | CV3623141 | single nucleotide variant | NM_153210.5(USP43):c.623C>T (p.Pro208Leu) | not specified [RCV004879487] | uncertain significance | 17 | 9656521 | 9656521 | Human | | name |
| 598210146 | CV3895037 | deletion | NM_153210.5(USP43):c.2336-957_2336-956del | Congenital heart disease [RCV005358492] | uncertain significance | 17 | 9726997 | 9726998 | Human | 1 | name |
| 8636417 | CV91642 | single nucleotide variant | NM_153210.4(USP43):c.515C>T (p.Ser172Phe) | Malignant melanoma [RCV000071740] | not provided | 17 | 9656413 | 9656413 | Human | | name |
| 156167255 | CV2200992 | single nucleotide variant | NM_153210.5(USP43):c.2731A>G (p.Thr911Ala) | not specified [RCV004074758] | likely benign | 17 | 9728349 | 9728349 | Human | | name |
| 156239839 | CV2221285 | single nucleotide variant | NM_153210.5(USP43):c.2764G>A (p.Asp922Asn) | not specified [RCV004094715] | uncertain significance | 17 | 9728382 | 9728382 | Human | | name |
| 155929053 | CV2224486 | single nucleotide variant | NM_153210.5(USP43):c.2110A>G (p.Ile704Val) | not specified [RCV004098077] | uncertain significance | 17 | 9710054 | 9710054 | Human | | name |
| 156074388 | CV2247820 | single nucleotide variant | NM_153210.5(USP43):c.1135C>T (p.Arg379Cys) | not specified [RCV004121284] | uncertain significance | 17 | 9682852 | 9682852 | Human | | name |
| 156217969 | CV2253907 | single nucleotide variant | NM_153210.5(USP43):c.1306A>G (p.Ile436Val) | not specified [RCV004127587] | uncertain significance | 17 | 9686862 | 9686862 | Human | | name |
| 155948771 | CV2273542 | single nucleotide variant | NM_153210.5(USP43):c.1789G>A (p.Glu597Lys) | not specified [RCV004134073] | uncertain significance | 17 | 9701478 | 9701478 | Human | | name |
| 155907571 | CV2302239 | single nucleotide variant | NM_153210.5(USP43):c.2642G>A (p.Arg881Gln) | not specified [RCV004159230] | uncertain significance | 17 | 9728260 | 9728260 | Human | | name |
| 156363271 | CV2329764 | single nucleotide variant | NM_153210.5(USP43):c.2368G>A (p.Val790Met) | not specified [RCV004183237] | uncertain significance | 17 | 9727986 | 9727986 | Human | | name |
| 156039653 | CV2332742 | single nucleotide variant | NM_153210.5(USP43):c.2078G>A (p.Arg693Gln) | not specified [RCV004189415] | uncertain significance | 17 | 9710022 | 9710022 | Human | | name |
| 156085482 | CV2340404 | single nucleotide variant | NM_153210.5(USP43):c.1430G>A (p.Arg477Gln) | not specified [RCV004197134] | uncertain significance | 17 | 9693203 | 9693203 | Human | | name |
| 156119625 | CV2354092 | single nucleotide variant | NM_153210.5(USP43):c.2363G>A (p.Arg788Gln) | not specified [RCV004206531] | uncertain significance | 17 | 9727981 | 9727981 | Human | | name |
| 155906152 | CV2357267 | single nucleotide variant | NM_153210.5(USP43):c.2446C>T (p.Arg816Trp) | not provided [RCV004695668]|not specified [RCV004200166] | uncertain significance | 17 | 9728064 | 9728064 | Human | | name |
| 156254782 | CV2358854 | single nucleotide variant | NM_153210.5(USP43):c.1903T>C (p.Ser635Pro) | not specified [RCV004212200] | uncertain significance | 17 | 9701592 | 9701592 | Human | | name |
| 156180515 | CV2374760 | single nucleotide variant | NM_153210.5(USP43):c.2072C>T (p.Pro691Leu) | not specified [RCV004225366] | uncertain significance | 17 | 9710016 | 9710016 | Human | | name |
| 155997774 | CV2398771 | single nucleotide variant | NM_153210.5(USP43):c.2846G>A (p.Gly949Asp) | not specified [RCV004240104] | uncertain significance | 17 | 9728464 | 9728464 | Human | | name |
| 156227063 | CV2401312 | single nucleotide variant | NM_153210.5(USP43):c.2722G>A (p.Gly908Ser) | not specified [RCV004245852] | uncertain significance | 17 | 9728340 | 9728340 | Human | | name |
| 329352205 | CV2452221 | single nucleotide variant | NM_153210.5(USP43):c.2368G>T (p.Val790Leu) | not specified [RCV004278921] | uncertain significance | 17 | 9727986 | 9727986 | Human | | name |
| 329395820 | CV2462978 | single nucleotide variant | NM_153210.5(USP43):c.2527C>T (p.Arg843Trp) | not specified [RCV004272810] | uncertain significance | 17 | 9728145 | 9728145 | Human | | name |
| 329398075 | CV2466662 | single nucleotide variant | NM_153210.5(USP43):c.1916C>G (p.Pro639Arg) | not specified [RCV004274178] | uncertain significance | 17 | 9701605 | 9701605 | Human | | name |
| 401736968 | CV2679193 | single nucleotide variant | NM_153210.5(USP43):c.2693A>C (p.Asn898Thr) | not specified [RCV004285752] | uncertain significance | 17 | 9728311 | 9728311 | Human | | name |
| 401752384 | CV2682801 | single nucleotide variant | NM_153210.5(USP43):c.1231C>A (p.Gln411Lys) | not specified [RCV004281773] | uncertain significance | 17 | 9682948 | 9682948 | Human | | name |
| 401745023 | CV2693163 | single nucleotide variant | NM_153210.5(USP43):c.2359G>A (p.Val787Ile) | not specified [RCV004293096] | uncertain significance | 17 | 9727977 | 9727977 | Human | | name |
| 401748123 | CV2700008 | single nucleotide variant | NM_153210.5(USP43):c.2462C>A (p.Ser821Tyr) | not specified [RCV004310437] | uncertain significance | 17 | 9728080 | 9728080 | Human | | name |
| 401721931 | CV2710240 | single nucleotide variant | NM_153210.5(USP43):c.2701C>G (p.Leu901Val) | not specified [RCV004317137] | uncertain significance | 17 | 9728319 | 9728319 | Human | | name |
| 401881094 | CV2763240 | single nucleotide variant | NM_153210.5(USP43):c.2342T>G (p.Leu781Trp) | not specified [RCV004336273] | uncertain significance | 17 | 9727960 | 9727960 | Human | | name |
| 401890995 | CV2768892 | single nucleotide variant | NM_153210.5(USP43):c.2837G>A (p.Arg946Gln) | not specified [RCV004346999] | uncertain significance | 17 | 9728455 | 9728455 | Human | | name |
| 405800830 | CV3338301 | single nucleotide variant | NM_153210.5(USP43):c.1042G>A (p.Ala348Thr) | not specified [RCV004477500] | uncertain significance | 17 | 9680303 | 9680303 | Human | | name |
| 405800832 | CV3338302 | single nucleotide variant | NM_153210.5(USP43):c.1193T>C (p.Val398Ala) | not specified [RCV004477501] | uncertain significance | 17 | 9682910 | 9682910 | Human | | name |
| 405800834 | CV3338303 | single nucleotide variant | NM_153210.5(USP43):c.1505C>T (p.Ala502Val) | not specified [RCV004477502] | uncertain significance | 17 | 9700219 | 9700219 | Human | | name |
| 405800838 | CV3338305 | single nucleotide variant | NM_153210.5(USP43):c.1940C>T (p.Pro647Leu) | not specified [RCV004477504] | uncertain significance | 17 | 9701629 | 9701629 | Human | | name |
| 405800840 | CV3338306 | single nucleotide variant | NM_153210.5(USP43):c.2014T>C (p.Tyr672His) | not specified [RCV004477505] | uncertain significance | 17 | 9709958 | 9709958 | Human | | name |
| 405800842 | CV3338307 | single nucleotide variant | NM_153210.5(USP43):c.2119T>C (p.Tyr707His) | not specified [RCV004477506] | uncertain significance | 17 | 9710063 | 9710063 | Human | | name |
| 405800844 | CV3338308 | single nucleotide variant | NM_153210.5(USP43):c.2171G>C (p.Gly724Ala) | not specified [RCV004477507] | uncertain significance | 17 | 9711968 | 9711968 | Human | | name |
| 405800846 | CV3338309 | single nucleotide variant | NM_153210.5(USP43):c.2473C>A (p.Pro825Thr) | not specified [RCV004477508] | uncertain significance | 17 | 9728091 | 9728091 | Human | | name |
| 405800848 | CV3338310 | single nucleotide variant | NM_153210.5(USP43):c.2561C>T (p.Thr854Met) | not specified [RCV004477509] | uncertain significance | 17 | 9728179 | 9728179 | Human | | name |
| 405800850 | CV3338311 | single nucleotide variant | NM_153210.5(USP43):c.2611G>A (p.Ala871Thr) | not specified [RCV004477510] | likely benign | 17 | 9728229 | 9728229 | Human | | name |
| 405800852 | CV3338312 | single nucleotide variant | NM_153210.5(USP43):c.2798T>G (p.Leu933Arg) | not specified [RCV004477511] | uncertain significance | 17 | 9728416 | 9728416 | Human | | name |
| 405800855 | CV3338314 | single nucleotide variant | NM_153210.5(USP43):c.2873G>A (p.Ser958Asn) | not specified [RCV004477513] | uncertain significance | 17 | 9728491 | 9728491 | Human | | name |
| 405800857 | CV3338315 | single nucleotide variant | NM_153210.5(USP43):c.2954C>T (p.Thr985Ile) | not specified [RCV004477514] | uncertain significance | 17 | 9728572 | 9728572 | Human | | name |
| 405800859 | CV3338316 | single nucleotide variant | NM_153210.5(USP43):c.2971C>T (p.Pro991Ser) | not specified [RCV004477515] | uncertain significance | 17 | 9728589 | 9728589 | Human | | name |
| 407528928 | CV3487669 | single nucleotide variant | NM_153210.5(USP43):c.1565C>T (p.Ala522Val) | not specified [RCV004680637] | likely benign | 17 | 9701148 | 9701148 | Human | | name |
| 407528930 | CV3487670 | single nucleotide variant | NM_153210.5(USP43):c.2244C>A (p.Ser748Arg) | not specified [RCV004680638] | uncertain significance | 17 | 9712041 | 9712041 | Human | | name |
| 407464630 | CV3487673 | single nucleotide variant | NM_153210.5(USP43):c.2688A>T (p.Gln896His) | not specified [RCV004688555] | likely benign | 17 | 9728306 | 9728306 | Human | | name |
| 407464634 | CV3487674 | single nucleotide variant | NM_153210.5(USP43):c.1026G>C (p.Glu342Asp) | not specified [RCV004688556] | uncertain significance | 17 | 9680287 | 9680287 | Human | | name |
| 597799229 | CV3623120 | single nucleotide variant | NM_153210.5(USP43):c.1581T>G (p.Ser527Arg) | not specified [RCV004879472] | uncertain significance | 17 | 9701164 | 9701164 | Human | | name |
| 597799225 | CV3623123 | single nucleotide variant | NM_153210.5(USP43):c.2914A>G (p.Met972Val) | not specified [RCV004879474] | likely benign | 17 | 9728532 | 9728532 | Human | | name |
| 597799224 | CV3623124 | single nucleotide variant | NM_153210.5(USP43):c.2021G>A (p.Arg674Gln) | not specified [RCV004879475] | uncertain significance | 17 | 9709965 | 9709965 | Human | | name |
| 597696661 | CV3623125 | single nucleotide variant | NM_153210.5(USP43):c.1429C>T (p.Arg477Trp) | not specified [RCV004885180] | uncertain significance | 17 | 9693202 | 9693202 | Human | | name |
| 597799219 | CV3623127 | single nucleotide variant | NM_153210.5(USP43):c.1708C>A (p.Gln570Lys) | not specified [RCV004879477] | uncertain significance | 17 | 9701397 | 9701397 | Human | | name |
| 597799215 | CV3623129 | single nucleotide variant | NM_153210.5(USP43):c.2922C>A (p.Phe974Leu) | not specified [RCV004879479] | likely benign | 17 | 9728540 | 9728540 | Human | | name |
| 597799213 | CV3623130 | single nucleotide variant | NM_153210.5(USP43):c.1562G>A (p.Arg521Gln) | not specified [RCV004879480] | uncertain significance | 17 | 9701145 | 9701145 | Human | | name |
| 597696668 | CV3623131 | single nucleotide variant | NM_153210.5(USP43):c.1148G>A (p.Arg383His) | not specified [RCV004885181] | uncertain significance | 17 | 9682865 | 9682865 | Human | | name |
| 597696674 | CV3623133 | single nucleotide variant | NM_153210.5(USP43):c.1115T>C (p.Leu372Pro) | not specified [RCV004885182] | likely benign | 17 | 9682832 | 9682832 | Human | | name |
| 597696683 | CV3623134 | single nucleotide variant | NM_153210.5(USP43):c.2842G>A (p.Glu948Lys) | not specified [RCV004885183] | uncertain significance | 17 | 9728460 | 9728460 | Human | | name |
| 597799209 | CV3623135 | single nucleotide variant | NM_153210.5(USP43):c.1007G>T (p.Arg336Leu) | not specified [RCV004879482] | uncertain significance | 17 | 9680268 | 9680268 | Human | | name |
| 597799206 | CV3623137 | single nucleotide variant | NM_153210.5(USP43):c.2366G>A (p.Gly789Asp) | not specified [RCV004879484] | uncertain significance | 17 | 9727984 | 9727984 | Human | | name |
| 597696692 | CV3623138 | single nucleotide variant | NM_153210.5(USP43):c.2906C>T (p.Ser969Phe) | not specified [RCV004885184] | uncertain significance | 17 | 9728524 | 9728524 | Human | | name |
| 597696702 | CV3623142 | single nucleotide variant | NM_153210.5(USP43):c.1127C>T (p.Ala376Val) | not specified [RCV004885185] | likely benign | 17 | 9682844 | 9682844 | Human | | name |
| 598238775 | CV3932903 | single nucleotide variant | NM_153210.5(USP43):c.1321C>T (p.Arg441Cys) | not specified [RCV005296472] | uncertain significance | 17 | 9686877 | 9686877 | Human | | name |
| 598204457 | CV3932904 | single nucleotide variant | NM_153210.5(USP43):c.2256G>C (p.Trp752Cys) | not specified [RCV005290694] | uncertain significance | 17 | 9712053 | 9712053 | Human | | name |
| 598204463 | CV3932905 | single nucleotide variant | NM_153210.5(USP43):c.2657G>T (p.Gly886Val) | not specified [RCV005290695] | likely benign | 17 | 9728275 | 9728275 | Human | | name |
| 598204468 | CV3932906 | single nucleotide variant | NM_153210.5(USP43):c.2333A>G (p.Lys778Arg) | not specified [RCV005290696] | uncertain significance | 17 | 9712130 | 9712130 | Human | | name |
| 598204474 | CV3932907 | single nucleotide variant | NM_153210.5(USP43):c.2605A>G (p.Asn869Asp) | not specified [RCV005290697] | uncertain significance | 17 | 9728223 | 9728223 | Human | | name |
| 8636418 | CV91643 | single nucleotide variant | NM_153210.4(USP43):c.2299C>T (p.Pro767Ser) | Malignant melanoma [RCV000071741] | not provided | 17 | 9712096 | 9712096 | Human | | name |
| 8636419 | CV91644 | single nucleotide variant | NM_153210.4(USP43):c.2531C>T (p.Ser844Phe) | Malignant melanoma [RCV000071742] | not provided | 17 | 9728149 | 9728149 | Human | | name |
| 329377112 | CV2435813 | single nucleotide variant | NM_153210.5(USP43):c.3004G>A (p.Val1002Met) | not specified [RCV004253434] | uncertain significance | 17 | 9728622 | 9728622 | Human | | name |
| 401735740 | CV2692187 | single nucleotide variant | NM_153210.5(USP43):c.3056A>G (p.Gln1019Arg) | not specified [RCV004301885] | uncertain significance | 17 | 9728674 | 9728674 | Human | | name |
| 405800861 | CV3338317 | single nucleotide variant | NM_153210.5(USP43):c.3097G>T (p.Ala1033Ser) | not specified [RCV004477516] | uncertain significance | 17 | 9728715 | 9728715 | Human | | name |
| 405800863 | CV3338318 | single nucleotide variant | NM_153210.5(USP43):c.3220C>T (p.Arg1074Cys) | not specified [RCV004477517] | uncertain significance | 17 | 9728838 | 9728838 | Human | | name |
| 405800865 | CV3338319 | single nucleotide variant | NM_153210.5(USP43):c.3341G>A (p.Arg1114Gln) | not specified [RCV004477518] | uncertain significance | 17 | 9728959 | 9728959 | Human | | name |
| 597696653 | CV3623121 | single nucleotide variant | NM_153210.5(USP43):c.3178G>A (p.Glu1060Lys) | not specified [RCV004885179] | uncertain significance | 17 | 9728796 | 9728796 | Human | | name |
| 597799211 | CV3623132 | single nucleotide variant | NM_153210.5(USP43):c.3139A>T (p.Ile1047Phe) | not specified [RCV004879481] | uncertain significance | 17 | 9728757 | 9728757 | Human | | name |
| 598204480 | CV3932908 | single nucleotide variant | NM_153210.5(USP43):c.3106G>C (p.Gly1036Arg) | not specified [RCV005290698] | uncertain significance | 17 | 9728724 | 9728724 | Human | | name |
| 15152575 | CV727626 | single nucleotide variant | NM_153210.5(USP43):c.3059T>C (p.Val1020Ala) | not provided [RCV000879835] | benign | 17 | 9728677 | 9728677 | Human | | name |
