| 8575988 | CV110343 | single nucleotide variant | NM_147193.2(GLIS1):c.-267+59809G>A | Lung cancer [RCV000090866] | uncertain significance | 1 | 53674095 | 53674095 | Human | | name |
| 15143931 | CV778807 | single nucleotide variant | NM_001367484.1(GLIS1):c.1593+10C>G | not provided [RCV000966752] | benign | 1 | 53524767 | 53524767 | Human | | name |
| 8625020 | CV80139 | single nucleotide variant | NM_147193.2(GLIS1):c.433C>T (p.Leu145=) | Malignant melanoma [RCV000060215] | not provided | 1 | 53594470 | 53594470 | Human | | name |
| 401927732 | CV2812810 | single nucleotide variant | NM_001367484.1(GLIS1):c.741C>T (p.Pro247=) | not provided [RCV003406502] | likely benign | 1 | 53594687 | 53594687 | Human | | name |
| 15175940 | CV707457 | single nucleotide variant | NM_001367484.1(GLIS1):c.759C>T (p.Ser253=) | not provided [RCV000973069] | benign | 1 | 53594669 | 53594669 | Human | | name |
| 15171553 | CV732511 | single nucleotide variant | NM_001367484.1(GLIS1):c.777C>G (p.Ser259=) | not provided [RCV000905491] | benign | 1 | 53594651 | 53594651 | Human | | name |
| 8629590 | CV84737 | single nucleotide variant | NM_147193.2(GLIS1):c.1483C>T (p.Pro495Ser) | Malignant melanoma [RCV000064819] | not provided | 1 | 53509903 | 53509903 | Human | | name |
| 596947966 | CV3547557 | single nucleotide variant | NM_001367484.1(GLIS1):c.1101C>T (p.Ala367=) | not provided [RCV004811861] | likely benign | 1 | 53594327 | 53594327 | Human | | name |
| 156037980 | CV2239608 | single nucleotide variant | NM_001367484.1(GLIS1):c.758C>T (p.Ser253Phe) | not specified [RCV004108170] | uncertain significance | 1 | 53594670 | 53594670 | Human | | name |
| 156072172 | CV2267425 | single nucleotide variant | NM_001367484.1(GLIS1):c.970C>T (p.Pro324Ser) | not specified [RCV004135860] | uncertain significance | 1 | 53594458 | 53594458 | Human | | name |
| 156252776 | CV2268416 | single nucleotide variant | NM_001367484.1(GLIS1):c.809C>T (p.Thr270Met) | not specified [RCV004132552] | likely benign | 1 | 53594619 | 53594619 | Human | | name |
| 156264706 | CV2289935 | single nucleotide variant | NM_001367484.1(GLIS1):c.887G>A (p.Arg296Gln) | not specified [RCV004150586] | uncertain significance | 1 | 53594541 | 53594541 | Human | | name |
| 156183877 | CV2339415 | single nucleotide variant | NM_001367484.1(GLIS1):c.926T>C (p.Leu309Ser) | not specified [RCV004191632] | uncertain significance | 1 | 53594502 | 53594502 | Human | | name |
| 156075233 | CV2350859 | single nucleotide variant | NM_001367484.1(GLIS1):c.581G>A (p.Gly194Asp) | not specified [RCV004211697] | uncertain significance | 1 | 53594847 | 53594847 | Human | | name |
| 156144119 | CV2393652 | single nucleotide variant | NM_001367484.1(GLIS1):c.563G>A (p.Arg188Gln) | not specified [RCV004231461] | uncertain significance | 1 | 53594865 | 53594865 | Human | | name |
| 401731538 | CV2701413 | single nucleotide variant | NM_001367484.1(GLIS1):c.616C>T (p.Leu206Phe) | not specified [RCV004311771] | uncertain significance | 1 | 53594812 | 53594812 | Human | | name |
| 401768733 | CV2735410 | single nucleotide variant | NM_001367484.1(GLIS1):c.715C>T (p.Arg239Trp) | not specified [RCV004334061] | uncertain significance | 1 | 53594713 | 53594713 | Human | | name |
| 401768755 | CV2735418 | single nucleotide variant | NM_001367484.1(GLIS1):c.697C>T (p.Pro233Ser) | not provided [RCV003410342]|not specified [RCV004330980] | likely benign|uncertain significance | 1 | 53594731 | 53594731 | Human | | name |
| 401893794 | CV2767022 | single nucleotide variant | NM_001367484.1(GLIS1):c.550T>A (p.Ser184Thr) | not specified [RCV004347435] | uncertain significance | 1 | 53594878 | 53594878 | Human | | name |
| 401895023 | CV2792690 | single nucleotide variant | NM_001367484.1(GLIS1):c.700G>A (p.Glu234Lys) | not specified [RCV004365468] | uncertain significance | 1 | 53594728 | 53594728 | Human | | name |
| 405753768 | CV3251791 | single nucleotide variant | NM_001367484.1(GLIS1):c.650G>A (p.Gly217Asp) | not specified [RCV004393138] | uncertain significance | 1 | 53594778 | 53594778 | Human | | name |
| 405753785 | CV3251794 | single nucleotide variant | NM_001367484.1(GLIS1):c.538C>T (p.Arg180Cys) | not specified [RCV004393141] | uncertain significance | 1 | 53594890 | 53594890 | Human | | name |
| 405753832 | CV3251800 | single nucleotide variant | NM_001367484.1(GLIS1):c.805C>A (p.Gln269Lys) | not specified [RCV004393147] | uncertain significance | 1 | 53594623 | 53594623 | Human | | name |
| 405753839 | CV3251801 | single nucleotide variant | NM_001367484.1(GLIS1):c.881G>A (p.Arg294Gln) | not specified [RCV004393148] | uncertain significance | 1 | 53594547 | 53594547 | Human | | name |
| 405753845 | CV3251802 | single nucleotide variant | NM_001367484.1(GLIS1):c.913C>T (p.His305Tyr) | not specified [RCV004393149] | uncertain significance | 1 | 53594515 | 53594515 | Human | | name |
| 407519711 | CV3443399 | single nucleotide variant | NM_001367484.1(GLIS1):c.905C>T (p.Thr302Met) | not specified [RCV004629729] | uncertain significance | 1 | 53594523 | 53594523 | Human | | name |
| 597729078 | CV3681362 | single nucleotide variant | NM_001367484.1(GLIS1):c.668G>A (p.Gly223Asp) | not specified [RCV004919661] | uncertain significance | 1 | 53594760 | 53594760 | Human | | name |
| 597759903 | CV3681363 | single nucleotide variant | NM_001367484.1(GLIS1):c.724G>A (p.Val242Ile) | not specified [RCV004925599] | uncertain significance | 1 | 53594704 | 53594704 | Human | | name |
| 598220884 | CV3977899 | single nucleotide variant | NM_001367484.1(GLIS1):c.694C>T (p.Leu232Phe) | not specified [RCV005340519] | uncertain significance | 1 | 53594734 | 53594734 | Human | | name |
| 598220891 | CV3977900 | single nucleotide variant | NM_001367484.1(GLIS1):c.797G>A (p.Arg266His) | not specified [RCV005340520] | uncertain significance | 1 | 53594631 | 53594631 | Human | | name |
| 598263611 | CV3977902 | single nucleotide variant | NM_001367484.1(GLIS1):c.924C>G (p.Ser308Arg) | not specified [RCV005348597] | uncertain significance | 1 | 53594504 | 53594504 | Human | | name |
| 598263617 | CV3977904 | single nucleotide variant | NM_001367484.1(GLIS1):c.806A>T (p.Gln269Leu) | not specified [RCV005348599] | uncertain significance | 1 | 53594622 | 53594622 | Human | | name |
| 15178251 | CV696797 | single nucleotide variant | NM_001367484.1(GLIS1):c.992T>C (p.Leu331Pro) | not provided [RCV000951234] | benign | 1 | 53594436 | 53594436 | Human | | name |
| 15155433 | CV707458 | single nucleotide variant | NM_001367484.1(GLIS1):c.673G>A (p.Gly225Ser) | not provided [RCV000968924] | benign | 1 | 53594755 | 53594755 | Human | | name |
| 155917380 | CV2202357 | single nucleotide variant | NM_001367484.1(GLIS1):c.1552G>A (p.Val518Ile) | not specified [RCV004078280] | uncertain significance | 1 | 53524818 | 53524818 | Human | | name |
| 155970165 | CV2213440 | single nucleotide variant | NM_001367484.1(GLIS1):c.1142A>G (p.Tyr381Cys) | not specified [RCV004087417] | uncertain significance | 1 | 53594286 | 53594286 | Human | | name |
| 156339824 | CV2229354 | single nucleotide variant | NM_001367484.1(GLIS1):c.2186G>A (p.Arg729Gln) | not specified [RCV004101142] | uncertain significance | 1 | 53509164 | 53509164 | Human | | name |
| 155986039 | CV2233951 | single nucleotide variant | NM_001367484.1(GLIS1):c.1709G>A (p.Gly570Asp) | not specified [RCV004104294] | uncertain significance | 1 | 53520651 | 53520651 | Human | | name |
| 155912225 | CV2235539 | single nucleotide variant | NM_001367484.1(GLIS1):c.1295C>T (p.Ser432Leu) | not specified [RCV004109571] | uncertain significance | 1 | 53594133 | 53594133 | Human | | name |
| 156026445 | CV2242354 | single nucleotide variant | NM_001367484.1(GLIS1):c.1943C>G (p.Pro648Arg) | not specified [RCV004111361] | uncertain significance | 1 | 53509968 | 53509968 | Human | | name |
| 156055689 | CV2243216 | single nucleotide variant | NM_001367484.1(GLIS1):c.2130A>C (p.Glu710Asp) | not specified [RCV004110106] | uncertain significance | 1 | 53509220 | 53509220 | Human | | name |
| 155960572 | CV2249437 | single nucleotide variant | NM_001367484.1(GLIS1):c.1889G>C (p.Gly630Ala) | not specified [RCV004120494] | uncertain significance | 1 | 53510022 | 53510022 | Human | | name |
| 156273628 | CV2254615 | single nucleotide variant | NM_001367484.1(GLIS1):c.2078T>C (p.Phe693Ser) | not specified [RCV004115110] | uncertain significance | 1 | 53509272 | 53509272 | Human | | name |
| 156129987 | CV2279749 | single nucleotide variant | NM_001367484.1(GLIS1):c.1241G>A (p.Arg414His) | not specified [RCV004144363] | uncertain significance | 1 | 53594187 | 53594187 | Human | | name |
| 156189956 | CV2328886 | single nucleotide variant | NM_001367484.1(GLIS1):c.1105C>T (p.Arg369Trp) | not specified [RCV004179885] | uncertain significance | 1 | 53594323 | 53594323 | Human | | name |
| 156331231 | CV2339607 | single nucleotide variant | NM_001367484.1(GLIS1):c.1962G>C (p.Gln654His) | not specified [RCV004196317] | uncertain significance | 1 | 53509949 | 53509949 | Human | | name |
| 156131545 | CV2358297 | single nucleotide variant | NM_001367484.1(GLIS1):c.1240C>G (p.Arg414Gly) | not specified [RCV004212080] | uncertain significance | 1 | 53594188 | 53594188 | Human | | name |
| 156263017 | CV2391639 | single nucleotide variant | NM_001367484.1(GLIS1):c.1106G>T (p.Arg369Leu) | not specified [RCV004241800] | uncertain significance | 1 | 53594322 | 53594322 | Human | | name |
| 329396033 | CV2451838 | single nucleotide variant | NM_001367484.1(GLIS1):c.1889G>A (p.Gly630Glu) | not specified [RCV004276520] | uncertain significance | 1 | 53510022 | 53510022 | Human | | name |
| 329401905 | CV2457971 | single nucleotide variant | NM_001367484.1(GLIS1):c.1102G>T (p.Gly368Trp) | not specified [RCV004271548] | uncertain significance | 1 | 53594326 | 53594326 | Human | | name |
| 329371288 | CV2458064 | single nucleotide variant | NM_001367484.1(GLIS1):c.1151A>G (p.Gln384Arg) | not specified [RCV004271896] | uncertain significance | 1 | 53594277 | 53594277 | Human | | name |
| 329370501 | CV2461741 | single nucleotide variant | NM_001367484.1(GLIS1):c.1774C>G (p.Leu592Val) | not specified [RCV004269889] | uncertain significance | 1 | 53514734 | 53514734 | Human | | name |
| 329392202 | CV2470471 | single nucleotide variant | NM_001367484.1(GLIS1):c.1984C>T (p.Pro662Ser) | not specified [RCV004273494] | uncertain significance | 1 | 53509927 | 53509927 | Human | | name |
| 401759424 | CV2701545 | single nucleotide variant | NM_001367484.1(GLIS1):c.2314G>C (p.Asp772His) | not specified [RCV004313989] | uncertain significance | 1 | 53506693 | 53506693 | Human | | name |
| 401720744 | CV2702086 | single nucleotide variant | NM_001367484.1(GLIS1):c.1024C>G (p.Pro342Ala) | not specified [RCV004320658] | uncertain significance | 1 | 53594404 | 53594404 | Human | | name |
| 401763616 | CV2720389 | single nucleotide variant | NM_001367484.1(GLIS1):c.1898T>C (p.Leu633Pro) | not specified [RCV004325697] | uncertain significance | 1 | 53510013 | 53510013 | Human | | name |
| 401879566 | CV2761799 | single nucleotide variant | NM_001367484.1(GLIS1):c.1196G>A (p.Arg399His) | not specified [RCV004339447] | uncertain significance | 1 | 53594232 | 53594232 | Human | | name |
| 401856154 | CV2764418 | single nucleotide variant | NM_001367484.1(GLIS1):c.2141G>T (p.Gly714Val) | not specified [RCV004338988] | uncertain significance | 1 | 53509209 | 53509209 | Human | | name |
| 401875699 | CV2766969 | single nucleotide variant | NM_001367484.1(GLIS1):c.1453G>A (p.Ala485Thr) | not specified [RCV004343353] | uncertain significance | 1 | 53529820 | 53529820 | Human | | name |
| 401886118 | CV2771084 | single nucleotide variant | NM_001367484.1(GLIS1):c.1204G>A (p.Glu402Lys) | not specified [RCV004346090] | uncertain significance | 1 | 53594224 | 53594224 | Human | | name |
| 401862514 | CV2771391 | single nucleotide variant | NM_001367484.1(GLIS1):c.1349G>A (p.Arg450Gln) | not specified [RCV004348449] | uncertain significance | 1 | 53529924 | 53529924 | Human | | name |
| 401892210 | CV2776001 | single nucleotide variant | NM_001367484.1(GLIS1):c.1757A>G (p.Asn586Ser) | not specified [RCV004345014] | uncertain significance | 1 | 53514751 | 53514751 | Human | | name |
| 401876071 | CV2777645 | single nucleotide variant | NM_001367484.1(GLIS1):c.2180C>T (p.Pro727Leu) | not specified [RCV004343485] | uncertain significance | 1 | 53509170 | 53509170 | Human | | name |
| 405753751 | CV3251789 | single nucleotide variant | NM_001367484.1(GLIS1):c.1582G>T (p.Val528Leu) | not specified [RCV004393136] | uncertain significance | 1 | 53524788 | 53524788 | Human | | name |
| 405753759 | CV3251790 | single nucleotide variant | NM_001367484.1(GLIS1):c.1742C>G (p.Ser581Cys) | not specified [RCV004393137] | uncertain significance | 1 | 53514766 | 53514766 | Human | | name |
| 405753778 | CV3251793 | single nucleotide variant | NM_001367484.1(GLIS1):c.1906C>A (p.Pro636Thr) | not specified [RCV004393140] | uncertain significance | 1 | 53510005 | 53510005 | Human | | name |
| 405753796 | CV3251795 | single nucleotide variant | NM_001367484.1(GLIS1):c.2094T>A (p.Ser698Arg) | not specified [RCV004393142] | uncertain significance | 1 | 53509256 | 53509256 | Human | | name |
| 405753801 | CV3251796 | single nucleotide variant | NM_001367484.1(GLIS1):c.2149G>A (p.Gly717Arg) | not specified [RCV004393143] | uncertain significance | 1 | 53509201 | 53509201 | Human | | name |
| 405753808 | CV3251797 | single nucleotide variant | NM_001367484.1(GLIS1):c.2158G>A (p.Gly720Arg) | not specified [RCV004393144] | uncertain significance | 1 | 53509192 | 53509192 | Human | | name |
| 405753816 | CV3251798 | single nucleotide variant | NM_001367484.1(GLIS1):c.2311G>A (p.Glu771Lys) | not specified [RCV004393145] | uncertain significance | 1 | 53506696 | 53506696 | Human | | name |
| 405753853 | CV3251803 | single nucleotide variant | NM_001367484.1(GLIS1):c.1151A>T (p.Gln384Leu) | not specified [RCV004393150] | uncertain significance | 1 | 53594277 | 53594277 | Human | | name |
| 405753867 | CV3251805 | single nucleotide variant | NM_001367484.1(GLIS1):c.1229G>A (p.Gly410Asp) | not specified [RCV004393152] | uncertain significance | 1 | 53594199 | 53594199 | Human | | name |
| 407519705 | CV3443396 | single nucleotide variant | NM_001367484.1(GLIS1):c.1025C>G (p.Pro342Arg) | not specified [RCV004629726] | uncertain significance | 1 | 53594403 | 53594403 | Human | | name |
| 407519707 | CV3443397 | single nucleotide variant | NM_001367484.1(GLIS1):c.1333A>G (p.Ser445Gly) | not specified [RCV004629727] | uncertain significance | 1 | 53529940 | 53529940 | Human | | name |
| 407519709 | CV3443398 | single nucleotide variant | NM_001367484.1(GLIS1):c.1519C>T (p.Arg507Cys) | not specified [RCV004629728] | uncertain significance | 1 | 53524851 | 53524851 | Human | | name |
| 407519714 | CV3443400 | single nucleotide variant | NM_001367484.1(GLIS1):c.2267C>T (p.Ala756Val) | not specified [RCV004629730] | uncertain significance | 1 | 53506740 | 53506740 | Human | | name |
| 407519716 | CV3443401 | single nucleotide variant | NM_001367484.1(GLIS1):c.1007A>G (p.Gln336Arg) | not specified [RCV004629731] | uncertain significance | 1 | 53594421 | 53594421 | Human | | name |
| 407519717 | CV3443402 | single nucleotide variant | NM_001367484.1(GLIS1):c.2347C>T (p.His783Tyr) | not specified [RCV004629732] | uncertain significance | 1 | 53506660 | 53506660 | Human | | name |
| 407519722 | CV3443403 | single nucleotide variant | NM_001367484.1(GLIS1):c.1999C>T (p.Pro667Ser) | not specified [RCV004629733] | uncertain significance | 1 | 53509912 | 53509912 | Human | | name |
| 407519725 | CV3443404 | single nucleotide variant | NM_001367484.1(GLIS1):c.1008G>C (p.Gln336His) | not specified [RCV004629734] | uncertain significance | 1 | 53594420 | 53594420 | Human | | name |
| 597729066 | CV3681358 | single nucleotide variant | NM_001367484.1(GLIS1):c.2176A>G (p.Asn726Asp) | not specified [RCV004919659] | uncertain significance | 1 | 53509174 | 53509174 | Human | | name |
| 597729072 | CV3681361 | single nucleotide variant | NM_001367484.1(GLIS1):c.1769C>T (p.Ser590Leu) | not specified [RCV004919660] | uncertain significance | 1 | 53514739 | 53514739 | Human | | name |
| 597729086 | CV3681364 | single nucleotide variant | NM_001367484.1(GLIS1):c.1188C>G (p.Ile396Met) | not specified [RCV004919662] | uncertain significance | 1 | 53594240 | 53594240 | Human | | name |
| 597729094 | CV3681365 | single nucleotide variant | NM_001367484.1(GLIS1):c.1906C>T (p.Pro636Ser) | not specified [RCV004919663] | uncertain significance | 1 | 53510005 | 53510005 | Human | | name |
| 597759908 | CV3681366 | single nucleotide variant | NM_001367484.1(GLIS1):c.1813C>T (p.Pro605Ser) | not specified [RCV004925600] | uncertain significance | 1 | 53514695 | 53514695 | Human | | name |
| 597759913 | CV3681367 | single nucleotide variant | NM_001367484.1(GLIS1):c.2009C>T (p.Pro670Leu) | not specified [RCV004925601] | uncertain significance | 1 | 53509902 | 53509902 | Human | | name |
| 597759918 | CV3681369 | single nucleotide variant | NM_001367484.1(GLIS1):c.1418G>A (p.Gly473Asp) | not specified [RCV004925602] | uncertain significance | 1 | 53529855 | 53529855 | Human | | name |
| 597729111 | CV3681370 | single nucleotide variant | NM_001367484.1(GLIS1):c.2030G>A (p.Ser677Asn) | not specified [RCV004919665] | uncertain significance | 1 | 53509881 | 53509881 | Human | | name |
| 597729118 | CV3681371 | single nucleotide variant | NM_001367484.1(GLIS1):c.1681A>G (p.Ser561Gly) | not specified [RCV004919666] | uncertain significance | 1 | 53520679 | 53520679 | Human | | name |
| 598263607 | CV3977901 | single nucleotide variant | NM_001367484.1(GLIS1):c.1046C>T (p.Pro349Leu) | not specified [RCV005348596] | uncertain significance | 1 | 53594382 | 53594382 | Human | | name |
| 598263614 | CV3977903 | single nucleotide variant | NM_001367484.1(GLIS1):c.1149G>T (p.Gln383His) | not specified [RCV005348598] | uncertain significance | 1 | 53594279 | 53594279 | Human | | name |
| 15183295 | CV707456 | single nucleotide variant | NM_001367484.1(GLIS1):c.1244A>G (p.Tyr415Cys) | not provided [RCV000974842] | benign | 1 | 53594184 | 53594184 | Human | | name |
