| 405731725 | CV3244529 | single nucleotide variant | NM_001130182.2(DNAJA4):c.-7A>G | not specified [RCV004379258] | likely benign | 15 | 78264757 | 78264757 | Human | | name |
| 401934339 | CV2814391 | single nucleotide variant | NM_001130182.2(DNAJA4):c.-14C>T | not provided [RCV003411196] | likely benign | 15 | 78264750 | 78264750 | Human | | name |
| 155926432 | CV2230614 | single nucleotide variant | NM_018602.4(DNAJA4):c.26G>C (p.Trp9Ser) | not specified [RCV004097572] | uncertain significance | 15 | 78264339 | 78264339 | Human | | name |
| 156244572 | CV2243137 | single nucleotide variant | NM_001130182.2(DNAJA4):c.58G>C (p.Glu20Gln) | not specified [RCV004110043] | uncertain significance | 15 | 78264821 | 78264821 | Human | | name |
| 156083247 | CV2249186 | single nucleotide variant | NM_001130182.2(DNAJA4):c.94A>C (p.Lys32Gln) | not specified [RCV004118233] | uncertain significance | 15 | 78264857 | 78264857 | Human | | name |
| 155959669 | CV2285302 | single nucleotide variant | NM_001130182.2(DNAJA4):c.84G>C (p.Lys28Asn) | not specified [RCV004139183] | uncertain significance | 15 | 78264847 | 78264847 | Human | | name |
| 405731290 | CV3244526 | single nucleotide variant | NM_001130182.2(DNAJA4):c.98A>G (p.Tyr33Cys) | not specified [RCV004379255] | uncertain significance | 15 | 78264861 | 78264861 | Human | | name |
| 597713817 | CV3662867 | single nucleotide variant | NM_001130182.2(DNAJA4):c.67A>G (p.Lys23Glu) | not specified [RCV004918066] | uncertain significance | 15 | 78264830 | 78264830 | Human | | name |
| 156333471 | CV2220841 | single nucleotide variant | NM_001130182.2(DNAJA4):c.205G>C (p.Glu69Gln) | not specified [RCV004092272] | uncertain significance | 15 | 78270569 | 78270569 | Human | | name |
| 156212207 | CV2259936 | single nucleotide variant | NM_001130182.2(DNAJA4):c.115C>G (p.Pro39Ala) | not specified [RCV004118961] | uncertain significance | 15 | 78264878 | 78264878 | Human | | name |
| 156144509 | CV2383935 | single nucleotide variant | NM_001130182.2(DNAJA4):c.292C>T (p.Arg98Trp) | not specified [RCV004231787] | uncertain significance | 15 | 78270656 | 78270656 | Human | | name |
| 597643565 | CV3662872 | single nucleotide variant | NM_001130182.2(DNAJA4):c.143T>C (p.Ile48Thr) | not specified [RCV004909508] | uncertain significance | 15 | 78270507 | 78270507 | Human | | name |
| 156256385 | CV2194567 | single nucleotide variant | NM_001130182.2(DNAJA4):c.830C>T (p.Thr277Met) | not specified [RCV004081627] | uncertain significance | 15 | 78275681 | 78275681 | Human | | name |
| 155931491 | CV2221042 | single nucleotide variant | NM_001130182.2(DNAJA4):c.337T>C (p.Ser113Pro) | not specified [RCV004092719] | uncertain significance | 15 | 78273118 | 78273118 | Human | | name |
| 155924814 | CV2248875 | single nucleotide variant | NM_001130182.2(DNAJA4):c.856C>G (p.Leu286Val) | not specified [RCV004115883] | uncertain significance | 15 | 78275707 | 78275707 | Human | | name |
| 156248946 | CV2277053 | single nucleotide variant | NM_001130182.2(DNAJA4):c.727G>A (p.Val243Met) | not specified [RCV004140373] | uncertain significance | 15 | 78275578 | 78275578 | Human | | name |
| 155970717 | CV2335609 | single nucleotide variant | NM_001130182.2(DNAJA4):c.620A>T (p.Lys207Met) | not specified [RCV004193814] | uncertain significance | 15 | 78274398 | 78274398 | Human | | name |
| 156013440 | CV2359101 | single nucleotide variant | NM_001130182.2(DNAJA4):c.469C>T (p.Arg157Trp) | not specified [RCV004214467] | uncertain significance | 15 | 78274247 | 78274247 | Human | | name |
| 155926367 | CV2365741 | single nucleotide variant | NM_001130182.2(DNAJA4):c.968T>C (p.Ile323Thr) | not specified [RCV004214283] | uncertain significance | 15 | 78280135 | 78280135 | Human | | name |
| 156338157 | CV2370580 | single nucleotide variant | NM_001130182.2(DNAJA4):c.371C>T (p.Thr124Met) | not specified [RCV004215909] | uncertain significance | 15 | 78273152 | 78273152 | Human | | name |
| 156077274 | CV2375093 | single nucleotide variant | NM_001130182.2(DNAJA4):c.602A>G (p.Lys201Arg) | not specified [RCV004230139] | uncertain significance | 15 | 78274380 | 78274380 | Human | | name |
| 156347999 | CV2375613 | single nucleotide variant | NM_001130182.2(DNAJA4):c.797A>C (p.Gln266Pro) | not specified [RCV004226096] | uncertain significance | 15 | 78275648 | 78275648 | Human | | name |
| 156195188 | CV2400471 | single nucleotide variant | NM_001130182.2(DNAJA4):c.772G>T (p.Asp258Tyr) | not specified [RCV004246673] | uncertain significance | 15 | 78275623 | 78275623 | Human | | name |
| 156004286 | CV2400970 | single nucleotide variant | NM_001130182.2(DNAJA4):c.559C>T (p.Arg187Cys) | not specified [RCV004244255] | uncertain significance | 15 | 78274337 | 78274337 | Human | | name |
| 329355106 | CV2449083 | single nucleotide variant | NM_001130182.2(DNAJA4):c.322G>A (p.Val108Ile) | not specified [RCV004264149] | uncertain significance | 15 | 78273103 | 78273103 | Human | | name |
| 405731297 | CV3244527 | single nucleotide variant | NM_001130182.2(DNAJA4):c.522C>G (p.Ile174Met) | not specified [RCV004379256] | uncertain significance | 15 | 78274300 | 78274300 | Human | | name |
| 405731306 | CV3244528 | single nucleotide variant | NM_001130182.2(DNAJA4):c.583G>A (p.Glu195Lys) | not specified [RCV004379257] | uncertain significance | 15 | 78274361 | 78274361 | Human | | name |
| 407497176 | CV3437470 | single nucleotide variant | NM_001130182.2(DNAJA4):c.498C>G (p.Ile166Met) | not specified [RCV004622133] | uncertain significance | 15 | 78274276 | 78274276 | Human | | name |
| 407497188 | CV3437473 | single nucleotide variant | NM_001130182.2(DNAJA4):c.477G>T (p.Met159Ile) | not specified [RCV004622136] | uncertain significance | 15 | 78274255 | 78274255 | Human | | name |
| 597713826 | CV3662868 | single nucleotide variant | NM_001130182.2(DNAJA4):c.913C>T (p.Arg305Cys) | not specified [RCV004918067] | uncertain significance | 15 | 78280080 | 78280080 | Human | | name |
| 597643558 | CV3662869 | single nucleotide variant | NM_001130182.2(DNAJA4):c.764G>A (p.Arg255Gln) | not specified [RCV004909507] | uncertain significance | 15 | 78275615 | 78275615 | Human | | name |
| 597713837 | CV3662870 | single nucleotide variant | NM_001130182.2(DNAJA4):c.595G>A (p.Gly199Arg) | not specified [RCV004918068] | uncertain significance | 15 | 78274373 | 78274373 | Human | | name |
| 597713848 | CV3662871 | single nucleotide variant | NM_001130182.2(DNAJA4):c.578G>T (p.Arg193Leu) | not specified [RCV004918069] | uncertain significance | 15 | 78274356 | 78274356 | Human | | name |
| 12896812 | CV390183 | deletion | NM_001130182.2(DNAJA4):c.132+1348_132+1349del | not specified [RCV000455856] | likely benign | 15 | 78266243 | 78266244 | Human | | name |
| 598162995 | CV3953419 | single nucleotide variant | NM_001130182.2(DNAJA4):c.725T>C (p.Ile242Thr) | not specified [RCV005329286] | uncertain significance | 15 | 78275576 | 78275576 | Human | | name |
| 598163008 | CV3953421 | single nucleotide variant | NM_001130182.2(DNAJA4):c.538G>A (p.Glu180Lys) | not specified [RCV005329288] | uncertain significance | 15 | 78274316 | 78274316 | Human | | name |
| 598163015 | CV3953422 | single nucleotide variant | NM_001130182.2(DNAJA4):c.854T>C (p.Ile285Thr) | not specified [RCV005329289] | uncertain significance | 15 | 78275705 | 78275705 | Human | | name |
| 156030492 | CV2238410 | single nucleotide variant | NM_001130182.2(DNAJA4):c.1187C>T (p.Thr396Met) | not specified [RCV004113474] | uncertain significance | 15 | 78280453 | 78280453 | Human | | name |
| 155950995 | CV2238695 | single nucleotide variant | NM_001130182.2(DNAJA4):c.1049G>C (p.Arg350Pro) | not specified [RCV004107589] | uncertain significance | 15 | 78280315 | 78280315 | Human | | name |
| 401774838 | CV2688305 | single nucleotide variant | NM_001130182.2(DNAJA4):c.1131C>A (p.His377Gln) | not specified [RCV004299313] | uncertain significance | 15 | 78280397 | 78280397 | Human | | name |
| 401766417 | CV2725528 | single nucleotide variant | NM_001130182.2(DNAJA4):c.1021C>T (p.Pro341Ser) | not specified [RCV004320144] | uncertain significance | 15 | 78280287 | 78280287 | Human | | name |
| 405731265 | CV3244523 | single nucleotide variant | NM_001130182.2(DNAJA4):c.1017G>T (p.Lys339Asn) | not specified [RCV004379252] | uncertain significance | 15 | 78280283 | 78280283 | Human | | name |
| 405731278 | CV3244525 | single nucleotide variant | NM_001130182.2(DNAJA4):c.1151A>G (p.Asp384Gly) | not specified [RCV004379254] | uncertain significance | 15 | 78280417 | 78280417 | Human | | name |
| 407497171 | CV3437469 | single nucleotide variant | NM_001130182.2(DNAJA4):c.1027C>G (p.Leu343Val) | not specified [RCV004622132] | uncertain significance | 15 | 78280293 | 78280293 | Human | | name |
| 407497184 | CV3437472 | single nucleotide variant | NM_001130182.2(DNAJA4):c.1048C>G (p.Arg350Gly) | not specified [RCV004622135] | uncertain significance | 15 | 78280314 | 78280314 | Human | | name |
| 597643572 | CV3662873 | single nucleotide variant | NM_001130182.2(DNAJA4):c.1076T>C (p.Met359Thr) | not specified [RCV004909509] | uncertain significance | 15 | 78280342 | 78280342 | Human | | name |
| 598163001 | CV3953420 | single nucleotide variant | NM_001130182.2(DNAJA4):c.1159G>A (p.Gly387Arg) | not specified [RCV005329287] | uncertain significance | 15 | 78280425 | 78280425 | Human | | name |