ClinVar Miner

List of variants in gene LTN1 reported as uncertain significance for not specified

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Gene type:
ClinVar version:
Total variants: 106
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HGVS dbSNP gnomAD frequency
NM_015565.3(LTN1):c.2731T>G (p.Ser911Ala) rs149472058 0.00096
NM_015565.3(LTN1):c.1781T>C (p.Val594Ala) rs140152516 0.00020
NM_015565.3(LTN1):c.3296G>A (p.Arg1099Gln) rs147272506 0.00020
NM_015565.3(LTN1):c.1000G>A (p.Val334Ile) rs376596181 0.00017
NM_015565.3(LTN1):c.1057C>T (p.Arg353Trp) rs139257092 0.00013
NM_015565.3(LTN1):c.2418A>C (p.Lys806Asn) rs140719641 0.00011
NM_015565.3(LTN1):c.3022G>T (p.Val1008Phe) rs200085542 0.00011
NM_015565.3(LTN1):c.3163C>A (p.Gln1055Lys) rs139261302 0.00011
NM_015565.3(LTN1):c.2093G>T (p.Arg698Ile) rs555391239 0.00007
NM_015565.3(LTN1):c.2953G>C (p.Asp985His) rs369347786 0.00006
NM_015565.3(LTN1):c.5120A>G (p.Lys1707Arg) rs370873711 0.00006
NM_015565.3(LTN1):c.1535T>C (p.Val512Ala) rs763361839 0.00005
NM_015565.3(LTN1):c.3212C>T (p.Ser1071Leu) rs528676722 0.00004
NM_015565.3(LTN1):c.4510C>T (p.Arg1504Trp) rs200123955 0.00004
NM_015565.3(LTN1):c.2284T>C (p.Ser762Pro) rs200714466 0.00003
NM_015565.3(LTN1):c.2398C>T (p.Leu800Phe) rs766875945 0.00003
NM_015565.3(LTN1):c.2949A>T (p.Lys983Asn) rs758481091 0.00003
NM_015565.3(LTN1):c.3536G>A (p.Ser1179Asn) rs201576214 0.00003
NM_015565.3(LTN1):c.3899C>A (p.Pro1300His) rs753105118 0.00003
NM_015565.3(LTN1):c.4330A>G (p.Ile1444Val) rs765555600 0.00003
NM_015565.3(LTN1):c.4415G>A (p.Cys1472Tyr) rs376529464 0.00003
NM_015565.3(LTN1):c.4596G>C (p.Glu1532Asp) rs763297583 0.00002
NM_015565.3(LTN1):c.-35G>A rs770378288 0.00001
NM_015565.3(LTN1):c.1361G>A (p.Gly454Glu) rs1419330062 0.00001
NM_015565.3(LTN1):c.1653G>C (p.Glu551Asp) rs370325007 0.00001
NM_015565.3(LTN1):c.1895T>C (p.Met632Thr) rs557102072 0.00001
NM_015565.3(LTN1):c.2087T>C (p.Met696Thr) rs770424631 0.00001
NM_015565.3(LTN1):c.2644T>A (p.Leu882Met) rs989620255 0.00001
NM_015565.3(LTN1):c.2815C>A (p.Leu939Ile) rs549637131 0.00001
NM_015565.3(LTN1):c.2830A>C (p.Ile944Leu) rs748611477 0.00001
NM_015565.3(LTN1):c.3179C>T (p.Thr1060Met) rs777774876 0.00001
NM_015565.3(LTN1):c.3268C>T (p.Leu1090Phe) rs941438558 0.00001
NM_015565.3(LTN1):c.3560A>G (p.His1187Arg) rs760752347 0.00001
NM_015565.3(LTN1):c.4141A>G (p.Thr1381Ala) rs755425794 0.00001
NM_015565.3(LTN1):c.4452A>G (p.Ile1484Met) rs778542604 0.00001
NM_015565.3(LTN1):c.913A>G (p.Ile305Val) rs772350288 0.00001
NM_015565.2(LTN1):c.65C>T (p.Ala22Val)
NM_015565.3(LTN1):c.-9A>G
NM_015565.3(LTN1):c.1058G>A (p.Arg353Gln)
NM_015565.3(LTN1):c.1118C>T (p.Ser373Phe) rs2516817267
NM_015565.3(LTN1):c.1134G>T (p.Lys378Asn)
NM_015565.3(LTN1):c.1186G>A (p.Glu396Lys)
NM_015565.3(LTN1):c.1327G>A (p.Asp443Asn) rs753323872
NM_015565.3(LTN1):c.1358A>G (p.His453Arg)
NM_015565.3(LTN1):c.1454A>G (p.Asn485Ser)
NM_015565.3(LTN1):c.1513C>G (p.Pro505Ala) rs1464449253
NM_015565.3(LTN1):c.1628A>T (p.Asp543Val) rs2516809405
NM_015565.3(LTN1):c.1666G>A (p.Val556Ile)
NM_015565.3(LTN1):c.1700A>T (p.Glu567Val) rs762976424
NM_015565.3(LTN1):c.1798A>G (p.Ile600Val)
NM_015565.3(LTN1):c.1837C>A (p.His613Asn)
NM_015565.3(LTN1):c.1841T>C (p.Leu614Pro)
NM_015565.3(LTN1):c.1856C>T (p.Thr619Ile)
NM_015565.3(LTN1):c.1868C>T (p.Ser623Phe) rs2516808489
NM_015565.3(LTN1):c.1903G>C (p.Gly635Arg) rs1344678836
NM_015565.3(LTN1):c.1919G>A (p.Ser640Asn) rs760516642
NM_015565.3(LTN1):c.1973C>T (p.Ala658Val)
NM_015565.3(LTN1):c.2033T>C (p.Phe678Ser) rs2084523940
NM_015565.3(LTN1):c.2036G>A (p.Gly679Asp)
NM_015565.3(LTN1):c.203T>C (p.Val68Ala)
NM_015565.3(LTN1):c.2050A>G (p.Ile684Val)
NM_015565.3(LTN1):c.2068C>T (p.Arg690Trp)
NM_015565.3(LTN1):c.2086A>T (p.Met696Leu) rs773418278
NM_015565.3(LTN1):c.208C>T (p.Arg70Trp)
NM_015565.3(LTN1):c.2122G>A (p.Val708Met)
NM_015565.3(LTN1):c.2215G>A (p.Asp739Asn) rs757419194
NM_015565.3(LTN1):c.2215G>C (p.Asp739His) rs757419194
NM_015565.3(LTN1):c.2218A>G (p.Ile740Val)
NM_015565.3(LTN1):c.2275T>A (p.Ser759Thr) rs2516793108
NM_015565.3(LTN1):c.2483A>G (p.Tyr828Cys)
NM_015565.3(LTN1):c.2560T>C (p.Cys854Arg) rs780481832
NM_015565.3(LTN1):c.2714A>C (p.Asn905Thr)
NM_015565.3(LTN1):c.2797G>C (p.Glu933Gln) rs1166255259
NM_015565.3(LTN1):c.2887A>G (p.Met963Val)
NM_015565.3(LTN1):c.2900A>C (p.His967Pro)
NM_015565.3(LTN1):c.2921G>T (p.Arg974Ile) rs2516782034
NM_015565.3(LTN1):c.2971A>T (p.Ile991Leu) rs1406758273
NM_015565.3(LTN1):c.3140T>G (p.Leu1047Arg) rs2516773332
NM_015565.3(LTN1):c.3194G>C (p.Arg1065Pro) rs571410562
NM_015565.3(LTN1):c.3200T>G (p.Leu1067Arg) rs761499413
NM_015565.3(LTN1):c.3529A>G (p.Thr1177Ala)
NM_015565.3(LTN1):c.3530C>T (p.Thr1177Ile)
NM_015565.3(LTN1):c.3544G>T (p.Asp1182Tyr) rs2516756568
NM_015565.3(LTN1):c.356G>A (p.Arg119His)
NM_015565.3(LTN1):c.3625A>C (p.Asn1209His)
NM_015565.3(LTN1):c.3710C>A (p.Ser1237Tyr) rs765760701
NM_015565.3(LTN1):c.3710C>T (p.Ser1237Phe) rs765760701
NM_015565.3(LTN1):c.3775A>G (p.Ser1259Gly) rs2516751651
NM_015565.3(LTN1):c.3840G>C (p.Leu1280Phe) rs2516751426
NM_015565.3(LTN1):c.3893A>G (p.Asn1298Ser)
NM_015565.3(LTN1):c.3910A>G (p.Ile1304Val)
NM_015565.3(LTN1):c.3930T>G (p.Phe1310Leu) rs768709019
NM_015565.3(LTN1):c.4166T>C (p.Leu1389Ser)
NM_015565.3(LTN1):c.4207C>T (p.His1403Tyr) rs2516748137
NM_015565.3(LTN1):c.4354G>A (p.Val1452Ile)
NM_015565.3(LTN1):c.4364G>A (p.Cys1455Tyr)
NM_015565.3(LTN1):c.4522A>G (p.Ser1508Gly) rs1405311910
NM_015565.3(LTN1):c.4835C>T (p.Ser1612Phe)
NM_015565.3(LTN1):c.4898G>A (p.Arg1633Gln)
NM_015565.3(LTN1):c.4946T>G (p.Ile1649Arg)
NM_015565.3(LTN1):c.5015C>T (p.Ala1672Val)
NM_015565.3(LTN1):c.5170G>A (p.Gly1724Ser)
NM_015565.3(LTN1):c.668G>A (p.Arg223Gln)
NM_015565.3(LTN1):c.703T>G (p.Leu235Val) rs1183393696
NM_015565.3(LTN1):c.73C>T (p.Leu25Phe)
NM_015565.3(LTN1):c.747G>T (p.Glu249Asp)

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