| 597694486 | CV3578268 | single nucleotide variant | NM_001114734.2(PABPC4L):c.-9G>C | not specified [RCV004838968] | uncertain significance | 4 | 134201028 | 134201028 | Human | | name |
| 156071979 | CV2233335 | single nucleotide variant | NM_001114734.2(PABPC4L):c.-89A>C | not specified [RCV004105708] | uncertain significance | 4 | 134201108 | 134201108 | Human | | name |
| 329356862 | CV2431173 | single nucleotide variant | NM_001114734.2(PABPC4L):c.-51G>A | not specified [RCV004250521] | likely benign | 4 | 134201070 | 134201070 | Human | | name |
| 405740593 | CV3371430 | single nucleotide variant | NM_001114734.2(PABPC4L):c.-19C>G | not specified [RCV004497679] | uncertain significance | 4 | 134201038 | 134201038 | Human | | name |
| 407517461 | CV3470027 | single nucleotide variant | NM_001114734.2(PABPC4L):c.-29G>A | not specified [RCV004650662] | uncertain significance | 4 | 134201048 | 134201048 | Human | | name |
| 597694540 | CV3578263 | single nucleotide variant | NM_001114734.2(PABPC4L):c.-66G>C | not specified [RCV004838963] | likely benign | 4 | 134201085 | 134201085 | Human | | name |
| 156191852 | CV2335943 | single nucleotide variant | NM_001114734.2(PABPC4L):c.-168G>A | not specified [RCV004189553] | uncertain significance | 4 | 134201187 | 134201187 | Human | | name |
| 407478768 | CV3470030 | single nucleotide variant | NM_001114734.2(PABPC4L):c.-170G>A | not specified [RCV004663980] | uncertain significance | 4 | 134201189 | 134201189 | Human | | name |
| 597694495 | CV3578267 | single nucleotide variant | NM_001114734.2(PABPC4L):c.-150G>A | not specified [RCV004838967] | uncertain significance | 4 | 134201169 | 134201169 | Human | | name |
| 597694465 | CV3578270 | single nucleotide variant | NM_001114734.2(PABPC4L):c.-152G>T | not specified [RCV004838970] | uncertain significance | 4 | 134201171 | 134201171 | Human | | name |
| 405740599 | CV3371431 | single nucleotide variant | NM_001114734.2(PABPC4L):c.1A>G (p.Met1Val) | not specified [RCV004497680] | uncertain significance | 4 | 134201019 | 134201019 | Human | | name |
| 401724386 | CV2677863 | single nucleotide variant | NM_001114734.2(PABPC4L):c.17A>G (p.Lys6Arg) | not specified [RCV004294358] | uncertain significance | 4 | 134201003 | 134201003 | Human | | name |
| 401883755 | CV2764556 | single nucleotide variant | NM_001114734.2(PABPC4L):c.56C>T (p.Ala19Val) | not specified [RCV004339111] | uncertain significance | 4 | 134200964 | 134200964 | Human | | name |
| 401738090 | CV2714320 | single nucleotide variant | NM_001114734.2(PABPC4L):c.151C>A (p.Leu51Met) | not specified [RCV004316000] | uncertain significance | 4 | 134200869 | 134200869 | Human | | name |
| 401887724 | CV2772114 | single nucleotide variant | NM_001114734.2(PABPC4L):c.106G>A (p.Val36Met) | not specified [RCV004344767] | uncertain significance | 4 | 134200914 | 134200914 | Human | | name |
| 405740608 | CV3371432 | single nucleotide variant | NM_001114734.2(PABPC4L):c.130G>A (p.Asp44Asn) | not specified [RCV004497681] | uncertain significance | 4 | 134200890 | 134200890 | Human | | name |
| 405740615 | CV3371433 | single nucleotide variant | NM_001114734.2(PABPC4L):c.214A>G (p.Asn72Asp) | not specified [RCV004497682] | uncertain significance | 4 | 134200806 | 134200806 | Human | | name |
| 405740619 | CV3371434 | single nucleotide variant | NM_001114734.2(PABPC4L):c.251T>C (p.Met84Thr) | not specified [RCV004497683] | uncertain significance | 4 | 134200769 | 134200769 | Human | | name |
| 405740627 | CV3371435 | single nucleotide variant | NM_001114734.2(PABPC4L):c.289A>C (p.Ile97Leu) | not specified [RCV004497684] | uncertain significance | 4 | 134200731 | 134200731 | Human | | name |
| 407478773 | CV3470031 | single nucleotide variant | NM_001114734.2(PABPC4L):c.158A>T (p.Tyr53Phe) | not specified [RCV004663981] | uncertain significance | 4 | 134200862 | 134200862 | Human | | name |
| 597694507 | CV3578266 | single nucleotide variant | NM_001114734.2(PABPC4L):c.184G>A (p.Ala62Thr) | not specified [RCV004838966] | likely benign | 4 | 134200836 | 134200836 | Human | | name |
| 597694475 | CV3578269 | single nucleotide variant | NM_001114734.2(PABPC4L):c.286G>A (p.Gly96Arg) | not specified [RCV004838969] | uncertain significance | 4 | 134200734 | 134200734 | Human | | name |
| 597694455 | CV3578271 | single nucleotide variant | NM_001114734.2(PABPC4L):c.208A>C (p.Thr70Pro) | not specified [RCV004838971] | uncertain significance | 4 | 134200812 | 134200812 | Human | | name |
| 156333836 | CV2266929 | single nucleotide variant | NM_001114734.2(PABPC4L):c.472A>G (p.Asn158Asp) | not specified [RCV004131589] | uncertain significance | 4 | 134200548 | 134200548 | Human | | name |
| 156100681 | CV2294728 | single nucleotide variant | NM_001114734.2(PABPC4L):c.605A>T (p.Asp202Val) | not specified [RCV004161967] | uncertain significance | 4 | 134200415 | 134200415 | Human | | name |
| 156191034 | CV2301773 | single nucleotide variant | NM_001114734.2(PABPC4L):c.412G>A (p.Gly138Ser) | not specified [RCV004156581] | uncertain significance | 4 | 134200608 | 134200608 | Human | | name |
| 156173117 | CV2326825 | single nucleotide variant | NM_001114734.2(PABPC4L):c.691G>T (p.Gly231Cys) | not specified [RCV004176658] | uncertain significance | 4 | 134200329 | 134200329 | Human | | name |
| 329364758 | CV2443834 | single nucleotide variant | NM_001114734.2(PABPC4L):c.649C>G (p.Leu217Val) | not specified [RCV004258175] | uncertain significance | 4 | 134200371 | 134200371 | Human | | name |
| 329351991 | CV2455582 | single nucleotide variant | NM_001114734.2(PABPC4L):c.320A>G (p.Lys107Arg) | not specified [RCV004276833] | uncertain significance | 4 | 134200700 | 134200700 | Human | | name |
| 401734273 | CV2688454 | single nucleotide variant | NM_001114734.2(PABPC4L):c.928C>G (p.Arg310Gly) | not specified [RCV004301436] | uncertain significance | 4 | 134200092 | 134200092 | Human | | name |
| 401735075 | CV2690768 | single nucleotide variant | NM_001114734.2(PABPC4L):c.766A>G (p.Asn256Asp) | not specified [RCV004298487] | uncertain significance | 4 | 134200254 | 134200254 | Human | | name |
| 405740582 | CV3371428 | single nucleotide variant | NM_001114734.2(PABPC4L):c.975G>T (p.Met325Ile) | not specified [RCV004497677] | uncertain significance | 4 | 134200045 | 134200045 | Human | | name |
| 405740631 | CV3371436 | single nucleotide variant | NM_001114734.2(PABPC4L):c.409A>G (p.Lys137Glu) | not specified [RCV004497685] | uncertain significance | 4 | 134200611 | 134200611 | Human | | name |
| 405740638 | CV3371437 | single nucleotide variant | NM_001114734.2(PABPC4L):c.529G>T (p.Asp177Tyr) | not specified [RCV004497686] | uncertain significance | 4 | 134200491 | 134200491 | Human | | name |
| 405740645 | CV3371438 | single nucleotide variant | NM_001114734.2(PABPC4L):c.606T>A (p.Asp202Glu) | not specified [RCV004497687] | uncertain significance | 4 | 134200414 | 134200414 | Human | | name |
| 405740654 | CV3371439 | single nucleotide variant | NM_001114734.2(PABPC4L):c.707G>C (p.Ser236Thr) | not specified [RCV004497688] | uncertain significance | 4 | 134200313 | 134200313 | Human | | name |
| 405740661 | CV3371440 | single nucleotide variant | NM_001114734.2(PABPC4L):c.716G>A (p.Ser239Asn) | not specified [RCV004497689] | uncertain significance | 4 | 134200304 | 134200304 | Human | | name |
| 407517464 | CV3470028 | single nucleotide variant | NM_001114734.2(PABPC4L):c.872A>G (p.Gln291Arg) | not specified [RCV004650663] | uncertain significance | 4 | 134200148 | 134200148 | Human | | name |
| 407478761 | CV3470029 | single nucleotide variant | NM_001114734.2(PABPC4L):c.552C>G (p.Ser184Arg) | not specified [RCV004663979] | uncertain significance | 4 | 134200468 | 134200468 | Human | | name |
| 407517467 | CV3470032 | single nucleotide variant | NM_001114734.2(PABPC4L):c.802A>C (p.Lys268Gln) | not specified [RCV004650664] | uncertain significance | 4 | 134200218 | 134200218 | Human | | name |
| 597694528 | CV3578264 | single nucleotide variant | NM_001114734.2(PABPC4L):c.460A>G (p.Ile154Val) | not specified [RCV004838964] | uncertain significance | 4 | 134200560 | 134200560 | Human | | name |
| 597694518 | CV3578265 | single nucleotide variant | NM_001114734.2(PABPC4L):c.750G>C (p.Met250Ile) | not specified [RCV004838965] | uncertain significance | 4 | 134200270 | 134200270 | Human | | name |
| 8631030 | CV86186 | single nucleotide variant | NM_001114734.1(PABPC4L):c.715G>A (p.Glu239Lys) | Malignant melanoma [RCV000066275] | not provided | 4 | 134200479 | 134200479 | Human | | name |
| 401744131 | CV2688102 | single nucleotide variant | NM_001114734.2(PABPC4L):c.1108C>T (p.His370Tyr) | not specified [RCV004305159] | likely benign | 4 | 134199912 | 134199912 | Human | | name |
| 405740588 | CV3371429 | single nucleotide variant | NM_001114734.2(PABPC4L):c.1036A>G (p.Thr346Ala) | not specified [RCV004497678] | uncertain significance | 4 | 134199984 | 134199984 | Human | | name |
| 598163800 | CV3995943 | single nucleotide variant | NM_001114734.2(PABPC4L):c.1037C>G (p.Thr346Ser) | not specified [RCV005391052] | uncertain significance | 4 | 134199983 | 134199983 | Human | | name |