| 155927519 | CV2285163 | single nucleotide variant | NM_153713.3(LIX1L):c.50G>A (p.Gly17Glu) | not specified [RCV004145376] | uncertain significance | 1 | 145957878 | 145957878 | Human | | name |
| 329357423 | CV2453589 | single nucleotide variant | NM_153713.3(LIX1L):c.98C>T (p.Ala33Val) | not specified [RCV004269258] | uncertain significance | 1 | 145957830 | 145957830 | Human | | name |
| 597623077 | CV3693189 | single nucleotide variant | NM_153713.3(LIX1L):c.89G>C (p.Gly30Ala) | not specified [RCV004936132] | uncertain significance | 1 | 145957839 | 145957839 | Human | | name |
| 597795876 | CV3693190 | single nucleotide variant | NM_153713.3(LIX1L):c.95C>T (p.Ala32Val) | not specified [RCV004935024] | uncertain significance | 1 | 145957833 | 145957833 | Human | | name |
| 155929164 | CV2224505 | single nucleotide variant | NM_153713.3(LIX1L):c.260G>A (p.Ser87Asn) | not specified [RCV004098093] | uncertain significance | 1 | 145957668 | 145957668 | Human | | name |
| 156000232 | CV2257729 | single nucleotide variant | NM_153713.3(LIX1L):c.154C>A (p.Pro52Thr) | not specified [RCV004127802] | uncertain significance | 1 | 145957774 | 145957774 | Human | | name |
| 156369374 | CV2263325 | single nucleotide variant | NM_153713.3(LIX1L):c.205G>A (p.Gly69Ser) | not specified [RCV004133599] | uncertain significance | 1 | 145957723 | 145957723 | Human | | name |
| 156162919 | CV2311860 | single nucleotide variant | NM_153713.3(LIX1L):c.128C>A (p.Pro43Gln) | not specified [RCV004170699] | uncertain significance | 1 | 145957800 | 145957800 | Human | | name |
| 156360349 | CV2329374 | single nucleotide variant | NM_153713.3(LIX1L):c.233G>C (p.Arg78Pro) | not specified [RCV004187390] | uncertain significance | 1 | 145957695 | 145957695 | Human | | name |
| 156048737 | CV2391034 | single nucleotide variant | NM_153713.3(LIX1L):c.278A>G (p.Gln93Arg) | not specified [RCV004235031] | uncertain significance | 1 | 145957650 | 145957650 | Human | | name |
| 329357421 | CV2453588 | single nucleotide variant | NM_153713.3(LIX1L):c.103A>G (p.Thr35Ala) | not specified [RCV004269257] | likely benign | 1 | 145957825 | 145957825 | Human | | name |
| 407470643 | CV3449133 | single nucleotide variant | NM_153713.3(LIX1L):c.115C>G (p.Pro39Ala) | not specified [RCV004637157] | uncertain significance | 1 | 145957813 | 145957813 | Human | | name |
| 597623075 | CV3693188 | single nucleotide variant | NM_153713.3(LIX1L):c.284A>G (p.Tyr95Cys) | not specified [RCV004936131] | uncertain significance | 1 | 145957644 | 145957644 | Human | | name |
| 597623079 | CV3693191 | single nucleotide variant | NM_153713.3(LIX1L):c.224C>T (p.Ala75Val) | not specified [RCV004936133] | uncertain significance | 1 | 145957704 | 145957704 | Human | | name |
| 156278749 | CV2210074 | single nucleotide variant | NM_153713.3(LIX1L):c.901G>C (p.Glu301Gln) | not specified [RCV004076503] | uncertain significance | 1 | 145936423 | 145936423 | Human | | name |
| 156195781 | CV2251886 | single nucleotide variant | NM_153713.3(LIX1L):c.612A>T (p.Glu204Asp) | not specified [RCV004119864] | uncertain significance | 1 | 145937685 | 145937685 | Human | | name |
| 156256057 | CV2277552 | single nucleotide variant | NM_153713.3(LIX1L):c.863C>T (p.Pro288Leu) | not specified [RCV004145239] | uncertain significance | 1 | 145936461 | 145936461 | Human | | name |
| 156191129 | CV2301782 | single nucleotide variant | NM_153713.3(LIX1L):c.920T>G (p.Leu307Arg) | not specified [RCV004156587] | uncertain significance | 1 | 145936404 | 145936404 | Human | | name |
| 156280666 | CV2321652 | single nucleotide variant | NM_153713.3(LIX1L):c.318A>C (p.Glu106Asp) | not specified [RCV004179662] | uncertain significance | 1 | 145947757 | 145947757 | Human | | name |
| 329378897 | CV2460029 | single nucleotide variant | NM_153713.3(LIX1L):c.548C>A (p.Thr183Asn) | not specified [RCV004279500] | uncertain significance | 1 | 145942762 | 145942762 | Human | | name |
| 329398337 | CV2464461 | single nucleotide variant | NM_153713.3(LIX1L):c.434G>A (p.Gly145Glu) | not specified [RCV004276383] | uncertain significance | 1 | 145947641 | 145947641 | Human | | name |
| 401779712 | CV2676663 | single nucleotide variant | NM_153713.3(LIX1L):c.575C>G (p.Ser192Cys) | not specified [RCV004290845] | uncertain significance | 1 | 145942735 | 145942735 | Human | | name |
| 401879737 | CV2788495 | single nucleotide variant | NM_153713.3(LIX1L):c.404C>T (p.Pro135Leu) | not specified [RCV004359477] | uncertain significance | 1 | 145947671 | 145947671 | Human | | name |
| 405809338 | CV3287511 | single nucleotide variant | NM_153713.3(LIX1L):c.389C>T (p.Pro130Leu) | not specified [RCV004407473] | uncertain significance | 1 | 145947686 | 145947686 | Human | | name |
| 405809340 | CV3287512 | single nucleotide variant | NM_153713.3(LIX1L):c.413G>C (p.Cys138Ser) | not specified [RCV004407474] | uncertain significance | 1 | 145947662 | 145947662 | Human | | name |
| 405809342 | CV3287513 | single nucleotide variant | NM_153713.3(LIX1L):c.670G>A (p.Gly224Ser) | not specified [RCV004407475] | uncertain significance | 1 | 145937627 | 145937627 | Human | | name |
| 405809344 | CV3287514 | single nucleotide variant | NM_153713.3(LIX1L):c.856A>C (p.Ser286Arg) | not specified [RCV004407476] | uncertain significance | 1 | 145936468 | 145936468 | Human | | name |
| 598260955 | CV3980942 | single nucleotide variant | NM_153713.3(LIX1L):c.481C>T (p.Arg161Trp) | not specified [RCV005347733] | uncertain significance | 1 | 145942829 | 145942829 | Human | | name |
| 598237694 | CV3980943 | single nucleotide variant | NM_153713.3(LIX1L):c.421A>C (p.Thr141Pro) | not specified [RCV005364124] | uncertain significance | 1 | 145947654 | 145947654 | Human | | name |
| 598260960 | CV3980944 | single nucleotide variant | NM_153713.3(LIX1L):c.818G>C (p.Arg273Pro) | not specified [RCV005347734] | uncertain significance | 1 | 145936506 | 145936506 | Human | | name |
