| 597798703 | CV3626359 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.7G>A (p.Val3Met) | not specified [RCV004879321] | uncertain significance | 1 | 109483960 | 109483960 | Human | | name |
| 401725108 | CV2725704 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.25G>A (p.Ala9Thr) | not specified [RCV004322401] | uncertain significance | 1 | 109483978 | 109483978 | Human | | name |
| 598231412 | CV3935919 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.17G>T (p.Arg6Leu) | not specified [RCV005295197] | uncertain significance | 1 | 109483970 | 109483970 | Human | | name |
| 329383891 | CV2434907 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.90C>G (p.Ser30Arg) | not specified [RCV004250781] | uncertain significance | 1 | 109484043 | 109484043 | Human | | name |
| 597798609 | CV3626294 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.56C>T (p.Pro19Leu) | not specified [RCV004879277] | uncertain significance | 1 | 109484009 | 109484009 | Human | | name |
| 156007827 | CV2365202 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.100G>A (p.Glu34Lys) | not specified [RCV004205215] | uncertain significance | 1 | 109484053 | 109484053 | Human | | name |
| 405678976 | CV3294201 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.215G>T (p.Cys72Phe) | not specified [RCV004421243] | uncertain significance | 1 | 109486527 | 109486527 | Human | | name |
| 598231279 | CV3935869 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.158C>T (p.Thr53Met) | not specified [RCV005295174] | likely benign | 1 | 109486087 | 109486087 | Human | | name |
| 598231395 | CV3935913 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.113T>G (p.Leu38Arg) | not specified [RCV005295194] | uncertain significance | 1 | 109484066 | 109484066 | Human | | name |
| 156124373 | CV2237332 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.964C>T (p.Arg322Cys) | not specified [RCV004104530] | uncertain significance | 1 | 109488931 | 109488931 | Human | | name |
| 155907020 | CV2302133 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.812T>G (p.Leu271Arg) | not specified [RCV004159148] | uncertain significance | 1 | 109488398 | 109488398 | Human | | name |
| 156343450 | CV2349093 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.325C>G (p.Leu109Val) | not specified [RCV004205939] | uncertain significance | 1 | 109487033 | 109487033 | Human | | name |
| 156257359 | CV2369375 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.701C>T (p.Pro234Leu) | not specified [RCV004208276] | uncertain significance | 1 | 109487709 | 109487709 | Human | | name |
| 405678981 | CV3294202 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.334C>T (p.Arg112Trp) | not specified [RCV004421244] | uncertain significance | 1 | 109487042 | 109487042 | Human | | name |
| 405678986 | CV3294203 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.461G>A (p.Arg154Gln) | not specified [RCV004421245] | uncertain significance | 1 | 109487169 | 109487169 | Human | | name |
| 405678993 | CV3294204 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.892C>A (p.His298Asn) | not specified [RCV004421246] | uncertain significance | 1 | 109488859 | 109488859 | Human | | name |
| 405678995 | CV3294205 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.934G>A (p.Val312Met) | not specified [RCV004421247] | uncertain significance | 1 | 109488901 | 109488901 | Human | | name |
| 407465569 | CV3488126 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.620T>G (p.Leu207Arg) | not specified [RCV004688804] | uncertain significance | 1 | 109487628 | 109487628 | Human | | name |
| 407455870 | CV3488190 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.691G>A (p.Glu231Lys) | not specified [RCV004685732] | uncertain significance | 1 | 109487699 | 109487699 | Human | | name |
| 597723268 | CV3626283 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.785G>A (p.Arg262Gln) | not specified [RCV004888067] | uncertain significance | 1 | 109487793 | 109487793 | Human | | name |
| 597723549 | CV3626349 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.847A>G (p.Lys283Glu) | not specified [RCV004888090] | uncertain significance | 1 | 109488433 | 109488433 | Human | | name |
| 597798716 | CV3626370 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.467G>A (p.Arg156His) | not specified [RCV004879327] | uncertain significance | 1 | 109487175 | 109487175 | Human | | name |
| 598254196 | CV3935891 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.655C>T (p.Pro219Ser) | not specified [RCV005299198] | uncertain significance | 1 | 109487663 | 109487663 | Human | | name |
| 156138228 | CV2202806 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1631G>C (p.Gly544Ala) | not specified [RCV004073665] | uncertain significance | 1 | 109491098 | 109491098 | Human | | name |
| 156301811 | CV2258562 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1285C>G (p.Pro429Ala) | not specified [RCV004116042] | uncertain significance | 1 | 109490081 | 109490081 | Human | | name |
| 156267486 | CV2275554 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.2167G>A (p.Ala723Thr) | not specified [RCV004137197] | uncertain significance | 1 | 109491634 | 109491634 | Human | | name |
| 156281014 | CV2295083 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1669T>C (p.Cys557Arg) | not specified [RCV004156194] | uncertain significance | 1 | 109491136 | 109491136 | Human | | name |
| 156306010 | CV2335059 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1301A>G (p.His434Arg) | not specified [RCV004184598] | uncertain significance | 1 | 109490097 | 109490097 | Human | | name |
| 156183104 | CV2338248 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1502C>G (p.Pro501Arg) | not specified [RCV004186308] | uncertain significance | 1 | 109490969 | 109490969 | Human | | name |
| 155937016 | CV2376227 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1388G>A (p.Arg463Gln) | not specified [RCV004220450] | uncertain significance | 1 | 109490326 | 109490326 | Human | | name |
| 329372707 | CV2428614 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1504T>A (p.Leu502Ile) | not specified [RCV004255420] | uncertain significance | 1 | 109490971 | 109490971 | Human | | name |
| 401743011 | CV2683992 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1222C>T (p.Arg408Trp) | not specified [RCV004295601] | uncertain significance | 1 | 109490018 | 109490018 | Human | | name |
| 401855790 | CV2757445 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1064C>T (p.Ala355Val) | not specified [RCV004340838] | uncertain significance | 1 | 109489031 | 109489031 | Human | | name |
| 401883330 | CV2760976 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.2194C>T (p.Arg732Cys) | not specified [RCV004338652] | uncertain significance | 1 | 109491661 | 109491661 | Human | | name |
| 401890166 | CV2763664 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.2075C>T (p.Thr692Ile) | not specified [RCV004343167] | uncertain significance | 1 | 109491542 | 109491542 | Human | | name |
| 401859903 | CV2768391 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1814A>G (p.Lys605Arg) | not specified [RCV004350641] | uncertain significance | 1 | 109491281 | 109491281 | Human | | name |
| 405678934 | CV3294192 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1144T>G (p.Ser382Ala) | not specified [RCV004421234] | uncertain significance | 1 | 109489940 | 109489940 | Human | | name |
| 405678938 | CV3294193 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1265G>A (p.Gly422Glu) | not specified [RCV004421235] | uncertain significance | 1 | 109490061 | 109490061 | Human | | name |
| 405678942 | CV3294194 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1502C>T (p.Pro501Leu) | not specified [RCV004421236] | uncertain significance | 1 | 109490969 | 109490969 | Human | | name |
| 405678947 | CV3294195 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1537A>T (p.Thr513Ser) | not specified [RCV004421237] | likely benign | 1 | 109491004 | 109491004 | Human | | name |
| 405678952 | CV3294196 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1724C>T (p.Pro575Leu) | not specified [RCV004421238] | uncertain significance | 1 | 109491191 | 109491191 | Human | | name |
| 405678957 | CV3294197 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1972C>A (p.Pro658Thr) | not specified [RCV004421239] | uncertain significance | 1 | 109491439 | 109491439 | Human | | name |
| 405678962 | CV3294198 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1976T>A (p.Leu659Gln) | not specified [RCV004421240] | uncertain significance | 1 | 109491443 | 109491443 | Human | | name |
| 405678967 | CV3294199 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.2018A>G (p.Lys673Arg) | not specified [RCV004421241] | uncertain significance | 1 | 109491485 | 109491485 | Human | | name |
| 405678972 | CV3294200 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.2020G>A (p.Ala674Thr) | not specified [RCV004421242] | uncertain significance | 1 | 109491487 | 109491487 | Human | | name |
| 405679003 | CV3294206 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1018G>A (p.Glu340Lys) | not specified [RCV004421248] | uncertain significance | 1 | 109488985 | 109488985 | Human | | name |
| 405679009 | CV3294207 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1021C>T (p.Arg341Cys) | not specified [RCV004421249] | uncertain significance | 1 | 109488988 | 109488988 | Human | | name |
| 407455746 | CV3488136 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1742C>T (p.Pro581Leu) | not specified [RCV004685688] | uncertain significance | 1 | 109491209 | 109491209 | Human | | name |
| 407455772 | CV3488147 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1766C>T (p.Ser589Phe) | not specified [RCV004685698] | uncertain significance | 1 | 109491233 | 109491233 | Human | | name |
| 407465593 | CV3488156 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1697C>T (p.Ser566Leu) | not specified [RCV004688810] | uncertain significance | 1 | 109491164 | 109491164 | Human | | name |
| 407455816 | CV3488168 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1478C>T (p.Pro493Leu) | not specified [RCV004685714] | uncertain significance | 1 | 109490945 | 109490945 | Human | | name |
| 407455843 | CV3488179 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1867G>A (p.Gly623Arg) | not specified [RCV004685723] | uncertain significance | 1 | 109491334 | 109491334 | Human | | name |
| 407455896 | CV3488200 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1945A>T (p.Met649Leu) | not specified [RCV004685741] | uncertain significance | 1 | 109491412 | 109491412 | Human | | name |
| 407455929 | CV3488211 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1946T>C (p.Met649Thr) | not specified [RCV004685752] | uncertain significance | 1 | 109491413 | 109491413 | Human | | name |
| 407572731 | CV3497220 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.2042G>T (p.Gly681Val) | not provided [RCV004699040] | uncertain significance | 1 | 109491509 | 109491509 | Human | | name |
| 597798619 | CV3626301 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1190G>A (p.Gly397Glu) | not specified [RCV004879282] | uncertain significance | 1 | 109489986 | 109489986 | Human | | name |
| 597798635 | CV3626310 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1286C>T (p.Pro429Leu) | not specified [RCV004879290] | likely benign | 1 | 109490082 | 109490082 | Human | | name |
| 597798646 | CV3626321 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1951C>T (p.Pro651Ser) | not specified [RCV004879295] | uncertain significance | 1 | 109491418 | 109491418 | Human | | name |
| 597798659 | CV3626331 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.2195G>A (p.Arg732His) | not specified [RCV004879301] | uncertain significance | 1 | 109491662 | 109491662 | Human | | name |
| 597723524 | CV3626341 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1172G>A (p.Gly391Asp) | not specified [RCV004888088] | uncertain significance | 1 | 109489968 | 109489968 | Human | | name |
| 598231357 | CV3935901 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1984C>T (p.Arg662Cys) | not specified [RCV005295187] | uncertain significance | 1 | 109491451 | 109491451 | Human | | name |
| 598231384 | CV3935910 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.1880C>A (p.Pro627His) | not specified [RCV005295192] | uncertain significance | 1 | 109491347 | 109491347 | Human | | name |
| 598231389 | CV3935911 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.2201A>G (p.Lys734Arg) | not specified [RCV005295193] | uncertain significance | 1 | 109491668 | 109491668 | Human | | name |
| 598254267 | CV3935912 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.2050G>A (p.Gly684Arg) | not specified [RCV005299208] | uncertain significance | 1 | 109491517 | 109491517 | Human | | name |
| 598231401 | CV3935915 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.2240C>G (p.Ser747Cys) | not specified [RCV005295195] | uncertain significance | 1 | 109491707 | 109491707 | Human | | name |
| 598254279 | CV3935916 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.2183C>T (p.Ala728Val) | not specified [RCV005299210] | uncertain significance | 1 | 109491650 | 109491650 | Human | | name |
| 598231406 | CV3935917 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.2189C>T (p.Ser730Phe) | not specified [RCV005295196] | uncertain significance | 1 | 109491656 | 109491656 | Human | | name |
| 598254285 | CV3935918 | single nucleotide variant | NM_001350175.2(ATXN7L2):c.2051G>T (p.Gly684Val) | not specified [RCV005299211] | uncertain significance | 1 | 109491518 | 109491518 | Human | | name |
