| 155990704 | CV2374790 | single nucleotide variant | NM_019030.4(DHX29):c.28G>C (p.Ala10Pro) | not specified [RCV004225393] | uncertain significance | 5 | 55307546 | 55307546 | Human | | name |
| 405692200 | CV3247139 | single nucleotide variant | NM_019030.4(DHX29):c.71G>C (p.Arg24Thr) | not specified [RCV004373518] | uncertain significance | 5 | 55307503 | 55307503 | Human | | name |
| 8631666 | CV86870 | single nucleotide variant | NM_019030.2(DHX29):c.639C>T (p.Asp213=) | Malignant melanoma [RCV000066961] | not provided | 5 | 55295391 | 55295391 | Human | | name |
| 155955987 | CV2387198 | single nucleotide variant | NM_019030.4(DHX29):c.139A>G (p.Thr47Ala) | not provided [RCV004696268]|not specified [RCV004238301] | uncertain significance | 5 | 55307435 | 55307435 | Human | | name |
| 401727400 | CV2680992 | single nucleotide variant | NM_019030.4(DHX29):c.263T>C (p.Val88Ala) | not specified [RCV004296060] | uncertain significance | 5 | 55297397 | 55297397 | Human | | name |
| 401767780 | CV2729909 | single nucleotide variant | NM_019030.4(DHX29):c.251C>A (p.Ser84Tyr) | not specified [RCV004332911] | uncertain significance | 5 | 55298601 | 55298601 | Human | | name |
| 405692139 | CV3247129 | single nucleotide variant | NM_019030.4(DHX29):c.284A>G (p.Glu95Gly) | not specified [RCV004373508] | uncertain significance | 5 | 55297376 | 55297376 | Human | | name |
| 598162304 | CV3953109 | single nucleotide variant | NM_019030.4(DHX29):c.253A>G (p.Ile85Val) | not specified [RCV005329144] | likely benign | 5 | 55298599 | 55298599 | Human | | name |
| 598162315 | CV3953111 | single nucleotide variant | NM_019030.4(DHX29):c.157G>A (p.Ala53Thr) | not specified [RCV005329146] | uncertain significance | 5 | 55307417 | 55307417 | Human | | name |
| 598162373 | CV3953121 | single nucleotide variant | NM_019030.4(DHX29):c.196A>G (p.Ile66Val) | not specified [RCV005329156] | uncertain significance | 5 | 55298656 | 55298656 | Human | | name |
| 9687043 | CV171401 | single nucleotide variant | NM_019030.4(DHX29):c.875A>T (p.Glu292Val) | Prostate cancer [RCV000149262] | uncertain significance | 5 | 55290250 | 55290250 | Human | 2 | name |
| 156237242 | CV2206834 | single nucleotide variant | NM_019030.4(DHX29):c.777C>A (p.Asp259Glu) | not specified [RCV004083508] | uncertain significance | 5 | 55294020 | 55294020 | Human | | name |
| 156184050 | CV2239113 | single nucleotide variant | NM_019030.4(DHX29):c.866G>C (p.Gly289Ala) | not specified [RCV004112112] | uncertain significance | 5 | 55290259 | 55290259 | Human | | name |
| 156145196 | CV2265032 | single nucleotide variant | NM_019030.4(DHX29):c.896A>G (p.Lys299Arg) | not specified [RCV004126190] | uncertain significance | 5 | 55290229 | 55290229 | Human | | name |
| 156210205 | CV2370209 | single nucleotide variant | NM_019030.4(DHX29):c.674T>C (p.Met225Thr) | not specified [RCV004211087] | likely benign | 5 | 55294123 | 55294123 | Human | | name |
| 156196982 | CV2400687 | single nucleotide variant | NM_019030.4(DHX29):c.641C>T (p.Pro214Leu) | not specified [RCV004242363] | uncertain significance | 5 | 55295389 | 55295389 | Human | | name |
| 329356431 | CV2430747 | single nucleotide variant | NM_019030.4(DHX29):c.670A>C (p.Asn224His) | not specified [RCV004253929] | uncertain significance | 5 | 55294127 | 55294127 | Human | | name |
| 401729485 | CV2683697 | single nucleotide variant | NM_019030.4(DHX29):c.550C>T (p.Pro184Ser) | not specified [RCV004284444] | uncertain significance | 5 | 55295480 | 55295480 | Human | | name |
| 401745454 | CV2693259 | single nucleotide variant | NM_019030.4(DHX29):c.451T>C (p.Tyr151His) | not specified [RCV004295229] | likely benign | 5 | 55296274 | 55296274 | Human | | name |
| 405692193 | CV3247138 | single nucleotide variant | NM_019030.4(DHX29):c.686T>C (p.Met229Thr) | not specified [RCV004373517] | uncertain significance | 5 | 55294111 | 55294111 | Human | | name |
| 405692206 | CV3247140 | single nucleotide variant | NM_019030.4(DHX29):c.763G>A (p.Glu255Lys) | not specified [RCV004373519] | uncertain significance | 5 | 55294034 | 55294034 | Human | | name |
| 597659499 | CV3652289 | single nucleotide variant | NM_019030.4(DHX29):c.815T>A (p.Leu272Gln) | not specified [RCV004911663] | uncertain significance | 5 | 55290310 | 55290310 | Human | | name |
| 597659506 | CV3652290 | single nucleotide variant | NM_019030.4(DHX29):c.980A>G (p.Lys327Arg) | not specified [RCV004911664] | uncertain significance | 5 | 55289356 | 55289356 | Human | | name |
| 598162322 | CV3953112 | single nucleotide variant | NM_019030.4(DHX29):c.584T>C (p.Ile195Thr) | not specified [RCV005329147] | uncertain significance | 5 | 55295446 | 55295446 | Human | | name |
| 598162350 | CV3953117 | single nucleotide variant | NM_019030.4(DHX29):c.757G>A (p.Glu253Lys) | not specified [RCV005329152] | uncertain significance | 5 | 55294040 | 55294040 | Human | | name |
| 13820730 | CV576116 | single nucleotide variant | NM_019030.4(DHX29):c.629A>G (p.Tyr210Cys) | not provided [RCV000709785] | not provided | 5 | 55295401 | 55295401 | Human | | name |
| 8626036 | CV81180 | single nucleotide variant | NM_019030.2(DHX29):c.520G>A (p.Gly174Arg) | Malignant melanoma [RCV000061258] | not provided | 5 | 55295510 | 55295510 | Human | | name |
| 156107116 | CV2214100 | single nucleotide variant | NM_019030.4(DHX29):c.2906T>C (p.Phe969Ser) | not specified [RCV004086108] | uncertain significance | 5 | 55270665 | 55270665 | Human | | name |
| 155945032 | CV2237918 | single nucleotide variant | NM_019030.4(DHX29):c.1073A>G (p.Lys358Arg) | not specified [RCV004109143] | uncertain significance | 5 | 55285855 | 55285855 | Human | | name |
| 156060082 | CV2239408 | single nucleotide variant | NM_019030.4(DHX29):c.2932C>T (p.Arg978Cys) | not specified [RCV004114136] | uncertain significance | 5 | 55270639 | 55270639 | Human | | name |
| 156215404 | CV2257569 | single nucleotide variant | NM_019030.4(DHX29):c.2869C>T (p.His957Tyr) | not specified [RCV004125614] | uncertain significance | 5 | 55270702 | 55270702 | Human | | name |
| 155967486 | CV2280416 | single nucleotide variant | NM_019030.4(DHX29):c.2524C>A (p.Pro842Thr) | not specified [RCV004140593] | uncertain significance | 5 | 55274914 | 55274914 | Human | | name |
| 156162049 | CV2311785 | single nucleotide variant | NM_019030.4(DHX29):c.2815A>G (p.Ile939Val) | not specified [RCV004170643] | uncertain significance | 5 | 55272136 | 55272136 | Human | | name |
| 155976310 | CV2342757 | single nucleotide variant | NM_019030.4(DHX29):c.1766G>A (p.Arg589Gln) | not specified [RCV004189801] | uncertain significance | 5 | 55283402 | 55283402 | Human | | name |
| 155934801 | CV2372543 | single nucleotide variant | NM_019030.4(DHX29):c.2740G>A (p.Ala914Thr) | not specified [RCV004219337] | uncertain significance | 5 | 55273328 | 55273328 | Human | | name |
| 155956649 | CV2387330 | single nucleotide variant | NM_019030.4(DHX29):c.2540T>C (p.Leu847Pro) | not specified [RCV004238415] | uncertain significance | 5 | 55274898 | 55274898 | Human | | name |
| 156157265 | CV2397944 | single nucleotide variant | NM_019030.4(DHX29):c.1576A>G (p.Asn526Asp) | not specified [RCV004241554] | uncertain significance | 5 | 55283592 | 55283592 | Human | | name |
| 155931840 | CV2399912 | single nucleotide variant | NM_019030.4(DHX29):c.1163G>C (p.Arg388Thr) | not specified [RCV004246853] | uncertain significance | 5 | 55285765 | 55285765 | Human | | name |
| 329400765 | CV2438766 | single nucleotide variant | NM_019030.4(DHX29):c.1159G>A (p.Val387Ile) | not specified [RCV004261907] | uncertain significance | 5 | 55285769 | 55285769 | Human | | name |
| 329351700 | CV2459294 | single nucleotide variant | NM_019030.4(DHX29):c.2098A>G (p.Ile700Val) | not specified [RCV004274721] | uncertain significance | 5 | 55281383 | 55281383 | Human | | name |
| 401740950 | CV2702712 | single nucleotide variant | NM_019030.4(DHX29):c.1817C>T (p.Pro606Leu) | not specified [RCV004318963] | uncertain significance | 5 | 55283351 | 55283351 | Human | | name |
| 401762874 | CV2707306 | single nucleotide variant | NM_019030.4(DHX29):c.2842A>G (p.Thr948Ala) | not specified [RCV004312712] | uncertain significance | 5 | 55272109 | 55272109 | Human | | name |
| 401738322 | CV2711783 | single nucleotide variant | NM_019030.4(DHX29):c.2139C>G (p.Phe713Leu) | not specified [RCV004309431] | uncertain significance | 5 | 55277253 | 55277253 | Human | | name |
| 401779804 | CV2714916 | single nucleotide variant | NM_019030.4(DHX29):c.2059C>A (p.Leu687Ile) | not specified [RCV004322248] | uncertain significance | 5 | 55281422 | 55281422 | Human | | name |
| 401876576 | CV2782968 | single nucleotide variant | NM_019030.4(DHX29):c.2335A>G (p.Lys779Glu) | not specified [RCV004361762] | uncertain significance | 5 | 55276358 | 55276358 | Human | | name |
| 401876328 | CV2785850 | single nucleotide variant | NM_019030.4(DHX29):c.2716A>G (p.Ile906Val) | not specified [RCV004365376] | uncertain significance | 5 | 55273352 | 55273352 | Human | | name |
| 405692086 | CV3247121 | single nucleotide variant | NM_019030.4(DHX29):c.1106A>G (p.Tyr369Cys) | not specified [RCV004373500] | uncertain significance | 5 | 55285822 | 55285822 | Human | | name |
| 405692098 | CV3247123 | single nucleotide variant | NM_019030.4(DHX29):c.1378C>G (p.Pro460Ala) | not specified [RCV004373502] | uncertain significance | 5 | 55283790 | 55283790 | Human | | name |
| 405692103 | CV3247124 | single nucleotide variant | NM_019030.4(DHX29):c.1676C>G (p.Thr559Arg) | not specified [RCV004373503] | uncertain significance | 5 | 55283492 | 55283492 | Human | | name |
| 405692111 | CV3247125 | single nucleotide variant | NM_019030.4(DHX29):c.2185C>T (p.His729Tyr) | not specified [RCV004373504] | uncertain significance | 5 | 55277207 | 55277207 | Human | | name |
| 405692117 | CV3247126 | single nucleotide variant | NM_019030.4(DHX29):c.2597T>G (p.Ile866Ser) | not specified [RCV004373505] | uncertain significance | 5 | 55274707 | 55274707 | Human | | name |
| 405692124 | CV3247127 | single nucleotide variant | NM_019030.4(DHX29):c.2767G>A (p.Val923Ile) | not specified [RCV004373506] | uncertain significance | 5 | 55273301 | 55273301 | Human | | name |
| 405692145 | CV3247130 | single nucleotide variant | NM_019030.4(DHX29):c.2975G>A (p.Arg992Gln) | not specified [RCV004373509] | uncertain significance | 5 | 55270596 | 55270596 | Human | | name |
| 407467270 | CV3434111 | single nucleotide variant | NM_019030.4(DHX29):c.1733G>A (p.Arg578Gln) | not specified [RCV004614172] | uncertain significance | 5 | 55283435 | 55283435 | Human | | name |
| 407467274 | CV3434112 | single nucleotide variant | NM_019030.4(DHX29):c.2293C>T (p.His765Tyr) | not specified [RCV004614173] | uncertain significance | 5 | 55276400 | 55276400 | Human | | name |
| 407467278 | CV3434113 | single nucleotide variant | NM_019030.4(DHX29):c.2828T>A (p.Val943Glu) | not specified [RCV004614174] | uncertain significance | 5 | 55272123 | 55272123 | Human | | name |
| 407467290 | CV3434116 | single nucleotide variant | NM_019030.4(DHX29):c.2027T>C (p.Leu676Pro) | not specified [RCV004614177] | uncertain significance | 5 | 55281454 | 55281454 | Human | | name |
| 597659448 | CV3652279 | single nucleotide variant | NM_019030.4(DHX29):c.1951G>C (p.Gly651Arg) | not specified [RCV004911654] | uncertain significance | 5 | 55283217 | 55283217 | Human | | name |
| 597659454 | CV3652280 | single nucleotide variant | NM_019030.4(DHX29):c.2026C>T (p.Leu676Phe) | not specified [RCV004911655] | uncertain significance | 5 | 55281455 | 55281455 | Human | | name |
| 597659459 | CV3652281 | single nucleotide variant | NM_019030.4(DHX29):c.1260T>A (p.Asp420Glu) | not specified [RCV004911656] | uncertain significance | 5 | 55285389 | 55285389 | Human | | name |
| 597659465 | CV3652282 | single nucleotide variant | NM_019030.4(DHX29):c.2441T>C (p.Val814Ala) | not specified [RCV004911657] | uncertain significance | 5 | 55274997 | 55274997 | Human | | name |
| 597659471 | CV3652283 | single nucleotide variant | NM_019030.4(DHX29):c.2150T>C (p.Ile717Thr) | not specified [RCV004911658] | uncertain significance | 5 | 55277242 | 55277242 | Human | | name |
| 597659478 | CV3652284 | single nucleotide variant | NM_019030.4(DHX29):c.1586C>T (p.Ser529Leu) | not specified [RCV004911659] | uncertain significance | 5 | 55283582 | 55283582 | Human | | name |
| 597659488 | CV3652287 | single nucleotide variant | NM_019030.4(DHX29):c.1964G>A (p.Arg655Lys) | not specified [RCV004911661] | likely benign | 5 | 55283204 | 55283204 | Human | | name |
| 597659493 | CV3652288 | single nucleotide variant | NM_019030.4(DHX29):c.2824G>A (p.Val942Ile) | not specified [RCV004911662] | uncertain significance | 5 | 55272127 | 55272127 | Human | | name |
| 597659513 | CV3652291 | single nucleotide variant | NM_019030.4(DHX29):c.2080A>C (p.Ser694Arg) | not specified [RCV004911665] | uncertain significance | 5 | 55281401 | 55281401 | Human | | name |
| 597659679 | CV3652294 | single nucleotide variant | NM_019030.4(DHX29):c.1081C>T (p.Pro361Ser) | not specified [RCV004911668] | uncertain significance | 5 | 55285847 | 55285847 | Human | | name |
| 597659698 | CV3652298 | single nucleotide variant | NM_019030.4(DHX29):c.1312C>A (p.His438Asn) | not specified [RCV004911672] | uncertain significance | 5 | 55285337 | 55285337 | Human | | name |
| 597659709 | CV3652300 | single nucleotide variant | NM_019030.4(DHX29):c.1279A>G (p.Thr427Ala) | not specified [RCV004911674] | uncertain significance | 5 | 55285370 | 55285370 | Human | | name |
| 598162298 | CV3953108 | single nucleotide variant | NM_019030.4(DHX29):c.1958G>C (p.Gly653Ala) | not specified [RCV005329143] | uncertain significance | 5 | 55283210 | 55283210 | Human | | name |
| 598162310 | CV3953110 | single nucleotide variant | NM_019030.4(DHX29):c.2617T>A (p.Phe873Ile) | not specified [RCV005329145] | uncertain significance | 5 | 55274687 | 55274687 | Human | | name |
| 598162334 | CV3953114 | single nucleotide variant | NM_019030.4(DHX29):c.2903C>T (p.Thr968Met) | not specified [RCV005329149] | uncertain significance | 5 | 55270668 | 55270668 | Human | | name |
| 598162339 | CV3953115 | single nucleotide variant | NM_019030.4(DHX29):c.1673G>A (p.Ser558Asn) | not specified [RCV005329150] | uncertain significance | 5 | 55283495 | 55283495 | Human | | name |
| 598162362 | CV3953119 | single nucleotide variant | NM_019030.4(DHX29):c.1262T>A (p.Val421Asp) | not specified [RCV005329154] | uncertain significance | 5 | 55285387 | 55285387 | Human | | name |
| 598162382 | CV3953123 | single nucleotide variant | NM_019030.4(DHX29):c.1733G>C (p.Arg578Pro) | not specified [RCV005329158] | uncertain significance | 5 | 55283435 | 55283435 | Human | | name |
| 598162393 | CV3953125 | single nucleotide variant | NM_019030.4(DHX29):c.2105A>G (p.Asp702Gly) | not specified [RCV005329160] | uncertain significance | 5 | 55281376 | 55281376 | Human | | name |
| 617153961 | CV4022081 | single nucleotide variant | NM_019030.4(DHX29):c.1199A>C (p.Glu400Ala) | not provided [RCV005429135] | not provided | 5 | 55285729 | 55285729 | Human | | name |
| 8631665 | CV86869 | single nucleotide variant | NM_019030.2(DHX29):c.2983A>G (p.Thr995Ala) | Malignant melanoma [RCV000066960] | not provided | 5 | 55270588 | 55270588 | Human | | name |
| 156248422 | CV2203115 | single nucleotide variant | NM_019030.4(DHX29):c.3410C>T (p.Thr1137Met) | not specified [RCV004069356] | uncertain significance | 5 | 55267707 | 55267707 | Human | | name |
| 156129155 | CV2238513 | single nucleotide variant | NM_019030.4(DHX29):c.3572C>T (p.Ser1191Leu) | not specified [RCV004107134] | uncertain significance | 5 | 55262886 | 55262886 | Human | | name |
| 156309210 | CV2249616 | single nucleotide variant | NM_019030.4(DHX29):c.4082C>T (p.Thr1361Met) | not specified [RCV004120626] | uncertain significance | 5 | 55256516 | 55256516 | Human | | name |
| 156203830 | CV2252443 | single nucleotide variant | NM_019030.4(DHX29):c.3559G>A (p.Ala1187Thr) | not specified [RCV004116565] | uncertain significance | 5 | 55262899 | 55262899 | Human | | name |
| 156138197 | CV2280647 | single nucleotide variant | NM_019030.4(DHX29):c.4054G>C (p.Glu1352Gln) | not specified [RCV004143118] | uncertain significance | 5 | 55259851 | 55259851 | Human | | name |
| 156126339 | CV2283703 | single nucleotide variant | NM_019030.4(DHX29):c.4015G>A (p.Val1339Ile) | not specified [RCV004142232] | uncertain significance | 5 | 55259890 | 55259890 | Human | | name |
| 156303459 | CV2308343 | single nucleotide variant | NM_019030.4(DHX29):c.3571T>C (p.Ser1191Pro) | not specified [RCV004164828] | uncertain significance | 5 | 55262887 | 55262887 | Human | | name |
| 401721166 | CV2673623 | single nucleotide variant | NM_019030.4(DHX29):c.3107A>T (p.Lys1036Ile) | not specified [RCV004282358] | uncertain significance | 5 | 55269600 | 55269600 | Human | | name |
| 401780989 | CV2681851 | single nucleotide variant | NM_019030.4(DHX29):c.3753A>C (p.Gln1251His) | not specified [RCV004296846] | uncertain significance | 5 | 55262705 | 55262705 | Human | | name |
| 401743687 | CV2684760 | single nucleotide variant | NM_019030.4(DHX29):c.3350G>A (p.Arg1117Gln) | not specified [RCV004293842] | uncertain significance | 5 | 55267767 | 55267767 | Human | | name |
| 401760684 | CV2715900 | single nucleotide variant | NM_019030.4(DHX29):c.3030C>G (p.Ile1010Met) | not specified [RCV004329008] | uncertain significance | 5 | 55270451 | 55270451 | Human | | name |
| 401861663 | CV2756400 | single nucleotide variant | NM_019030.4(DHX29):c.3925C>T (p.Arg1309Cys) | not specified [RCV004342942] | uncertain significance | 5 | 55261403 | 55261403 | Human | | name |
| 401881412 | CV2759406 | single nucleotide variant | NM_019030.4(DHX29):c.3343A>G (p.Ile1115Val) | not specified [RCV004338407] | uncertain significance | 5 | 55267774 | 55267774 | Human | | name |
| 401866721 | CV2782925 | single nucleotide variant | NM_019030.4(DHX29):c.3910G>A (p.Val1304Ile) | not specified [RCV004361724] | uncertain significance | 5 | 55261418 | 55261418 | Human | | name |
| 401864954 | CV2791429 | single nucleotide variant | NM_019030.4(DHX29):c.4048T>C (p.Ser1350Pro) | not specified [RCV004358820] | uncertain significance | 5 | 55259857 | 55259857 | Human | | name |
| 401872615 | CV2793128 | single nucleotide variant | NM_019030.4(DHX29):c.3866T>G (p.Leu1289Arg) | not specified [RCV004360441] | uncertain significance | 5 | 55261462 | 55261462 | Human | | name |
| 405692149 | CV3247131 | single nucleotide variant | NM_019030.4(DHX29):c.3138C>G (p.Ile1046Met) | not specified [RCV004373510] | uncertain significance | 5 | 55269569 | 55269569 | Human | | name |
| 405692155 | CV3247132 | single nucleotide variant | NM_019030.4(DHX29):c.3248G>A (p.Gly1083Asp) | not specified [RCV004373511] | uncertain significance | 5 | 55269459 | 55269459 | Human | | name |
| 405692164 | CV3247133 | single nucleotide variant | NM_019030.4(DHX29):c.3346G>T (p.Gly1116Cys) | not specified [RCV004373512] | uncertain significance | 5 | 55267771 | 55267771 | Human | | name |
| 405692169 | CV3247134 | single nucleotide variant | NM_019030.4(DHX29):c.3410C>A (p.Thr1137Lys) | not specified [RCV004373513] | uncertain significance | 5 | 55267707 | 55267707 | Human | | name |
| 405692745 | CV3247135 | single nucleotide variant | NM_019030.4(DHX29):c.3484C>T (p.Arg1162Trp) | not specified [RCV004373514] | uncertain significance | 5 | 55267179 | 55267179 | Human | | name |
| 405692182 | CV3247136 | single nucleotide variant | NM_019030.4(DHX29):c.3739G>A (p.Val1247Met) | not specified [RCV004373515] | uncertain significance | 5 | 55262719 | 55262719 | Human | | name |
| 405692187 | CV3247137 | single nucleotide variant | NM_019030.4(DHX29):c.4000G>A (p.Val1334Ile) | not specified [RCV004373516] | uncertain significance | 5 | 55259905 | 55259905 | Human | | name |
| 407467282 | CV3434114 | single nucleotide variant | NM_019030.4(DHX29):c.3771C>A (p.His1257Gln) | not specified [RCV004614175] | uncertain significance | 5 | 55262687 | 55262687 | Human | | name |
| 407467286 | CV3434115 | single nucleotide variant | NM_019030.4(DHX29):c.3827A>G (p.Lys1276Arg) | not specified [RCV004614176] | uncertain significance | 5 | 55262631 | 55262631 | Human | | name |
| 597659669 | CV3652292 | single nucleotide variant | NM_019030.4(DHX29):c.3856G>C (p.Glu1286Gln) | not specified [RCV004911666] | uncertain significance | 5 | 55261472 | 55261472 | Human | | name |
| 597659674 | CV3652293 | single nucleotide variant | NM_019030.4(DHX29):c.3362C>T (p.Ala1121Val) | not specified [RCV004911667] | uncertain significance | 5 | 55267755 | 55267755 | Human | | name |
| 597659684 | CV3652295 | single nucleotide variant | NM_019030.4(DHX29):c.3082G>C (p.Gly1028Arg) | not specified [RCV004911669] | uncertain significance | 5 | 55269625 | 55269625 | Human | | name |
| 597659694 | CV3652297 | single nucleotide variant | NM_019030.4(DHX29):c.3487A>G (p.Arg1163Gly) | not specified [RCV004911671] | uncertain significance | 5 | 55267176 | 55267176 | Human | | name |
| 597659705 | CV3652299 | single nucleotide variant | NM_019030.4(DHX29):c.3562G>A (p.Ala1188Thr) | not specified [RCV004911673] | uncertain significance | 5 | 55262896 | 55262896 | Human | | name |
| 598162329 | CV3953113 | single nucleotide variant | NM_019030.4(DHX29):c.3587C>G (p.Ser1196Cys) | not specified [RCV005329148] | uncertain significance | 5 | 55262871 | 55262871 | Human | | name |
| 598162356 | CV3953118 | single nucleotide variant | NM_019030.4(DHX29):c.4034A>C (p.Glu1345Ala) | not specified [RCV005329153] | uncertain significance | 5 | 55259871 | 55259871 | Human | | name |
| 598162367 | CV3953120 | single nucleotide variant | NM_019030.4(DHX29):c.4064A>G (p.Lys1355Arg) | not specified [RCV005329155] | uncertain significance | 5 | 55256534 | 55256534 | Human | | name |
| 598162377 | CV3953122 | single nucleotide variant | NM_019030.4(DHX29):c.3653C>T (p.Ala1218Val) | not specified [RCV005329157] | uncertain significance | 5 | 55262805 | 55262805 | Human | | name |
| 598162387 | CV3953124 | single nucleotide variant | NM_019030.4(DHX29):c.3538G>A (p.Glu1180Lys) | not specified [RCV005329159] | uncertain significance | 5 | 55262920 | 55262920 | Human | | name |
