ClinVar Miner

List of variants in gene ALG13 reported as likely benign

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Gene type:
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Total variants: 149
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HGVS dbSNP
NM_001099922.3(ALG13):c.-14G>A rs199642821
NM_001099922.3(ALG13):c.-27G>A rs201622950
NM_001099922.3(ALG13):c.-7C>T rs188487746
NM_001099922.3(ALG13):c.-9A>G rs374253660
NM_001099922.3(ALG13):c.1006-14G>A rs760527824
NM_001099922.3(ALG13):c.1029T>C (p.Ser343=) rs772765360
NM_001099922.3(ALG13):c.104A>G (p.Asn35Ser) rs149808406
NM_001099922.3(ALG13):c.1087+18A>G rs374773161
NM_001099922.3(ALG13):c.108A>G (p.Arg36=) rs769838471
NM_001099922.3(ALG13):c.1182G>A (p.Lys394=) rs1602694246
NM_001099922.3(ALG13):c.1183A>C (p.Asn395His) rs1602694279
NM_001099922.3(ALG13):c.1211A>C (p.Glu404Ala) rs1569517608
NM_001099922.3(ALG13):c.1221T>C (p.His407=) rs1602694489
NM_001099922.3(ALG13):c.1251-4T>C rs1602705501
NM_001099922.3(ALG13):c.1277A>G (p.Asn426Ser) rs1208820400
NM_001099922.3(ALG13):c.1304A>G (p.Asn435Ser) rs747478031
NM_001099922.3(ALG13):c.1308A>G (p.Lys436=) rs1423402192
NM_001099922.3(ALG13):c.1313C>A (p.Thr438Lys) rs367783946
NM_001099922.3(ALG13):c.1327-19A>G rs375412069
NM_001099922.3(ALG13):c.1388A>G (p.Glu463Gly) rs184599884
NM_001099922.3(ALG13):c.139G>A (p.Val47Ile) rs766512298
NM_001099922.3(ALG13):c.13T>C (p.Phe5Leu) rs199754211
NM_001099922.3(ALG13):c.1435+11A>G rs1556499962
NM_001099922.3(ALG13):c.150C>T (p.Pro50=) rs147897682
NM_001099922.3(ALG13):c.1591T>C (p.Leu531=) rs112837367
NM_001099922.3(ALG13):c.1596G>A (p.Ala532=) rs891310320
NM_001099922.3(ALG13):c.1601+11G>A rs770867470
NM_001099922.3(ALG13):c.1707T>C (p.Pro569=) rs1602730890
NM_001099922.3(ALG13):c.1729+14A>G rs763484848
NM_001099922.3(ALG13):c.1747A>G (p.Ile583Val) rs377397506
NM_001099922.3(ALG13):c.1798A>G (p.Met600Val) rs189931917
NM_001099922.3(ALG13):c.1812C>T (p.Tyr604=) rs768241839
NM_001099922.3(ALG13):c.1824C>T (p.Asp608=) rs761077008
NM_001099922.3(ALG13):c.1831C>G (p.Leu611Val) rs199505558
NM_001099922.3(ALG13):c.1831C>T (p.Leu611Phe) rs199505558
NM_001099922.3(ALG13):c.1843C>T (p.Leu615=) rs374231091
NM_001099922.3(ALG13):c.1869C>T (p.His623=) rs747208594
NM_001099922.3(ALG13):c.1910T>C (p.Met637Thr) rs774331771
NM_001099922.3(ALG13):c.1922A>G (p.His641Arg) rs766772102
NM_001099922.3(ALG13):c.1976+20G>A rs1556507692
NM_001099922.3(ALG13):c.1977-12C>T rs374618611
NM_001099922.3(ALG13):c.2004C>T (p.His668=) rs1024835814
NM_001099922.3(ALG13):c.2013G>A (p.Pro671=) rs775697727
NM_001099922.3(ALG13):c.2070T>C (p.Asp690=) rs371239344
NM_001099922.3(ALG13):c.2082T>C (p.Tyr694=) rs778640194
NM_001099922.3(ALG13):c.2091-8C>G rs939425312
NM_001099922.3(ALG13):c.2142G>A (p.Gln714=) rs1602749741
NM_001099922.3(ALG13):c.2205T>C (p.Tyr735=) rs1060503802
NM_001099922.3(ALG13):c.2248-11C>T rs377064873
NM_001099922.3(ALG13):c.2248-15G>C rs139711892
NM_001099922.3(ALG13):c.2248-25GT[7] rs757486083
NM_001099922.3(ALG13):c.2248-42A>G rs147250361
NM_001099922.3(ALG13):c.2266A>G (p.Thr756Ala) rs748648454
NM_001099922.3(ALG13):c.2324A>G (p.Lys775Arg) rs766946325
NM_001099922.3(ALG13):c.2368+10T>G rs1556509952
NM_001099922.3(ALG13):c.2369-4_2369-3del rs1064795371
NM_001099922.3(ALG13):c.2369-7dup rs1556512668
NM_001099922.3(ALG13):c.2369G>A (p.Gly790Glu) rs745411126
NM_001099922.3(ALG13):c.2380_2382GAA[1] (p.Glu795del) rs772766102
NM_001099922.3(ALG13):c.2385A>G (p.Glu795=) rs759719376
NM_001099922.3(ALG13):c.2401+9G>T rs1036320277
NM_001099922.3(ALG13):c.244+5_244+6insC rs1556445112
NM_001099922.3(ALG13):c.244+7G>T rs1556445122
NM_001099922.3(ALG13):c.2457+15_2457+17del rs761459857
NM_001099922.3(ALG13):c.2475G>A (p.Lys825=) rs1298792527
NM_001099922.3(ALG13):c.2485A>G (p.Met829Val) rs368075878
NM_001099922.3(ALG13):c.2500A>G (p.Thr834Ala)
NM_001099922.3(ALG13):c.2529+275C>T rs16986620
NM_001099922.3(ALG13):c.2529+6C>G rs1569520797
NM_001099922.3(ALG13):c.2530-310G>T rs142085120
NM_001099922.3(ALG13):c.2570A>G (p.Asn857Ser) rs1556516921
NM_001099922.3(ALG13):c.2607G>A (p.Ala869=) rs746842727
NM_001099922.3(ALG13):c.2617G>C (p.Ala873Pro) rs142841538
NM_001099922.3(ALG13):c.2654T>C (p.Ile885Thr) rs781459134
NM_001099922.3(ALG13):c.2695+15G>C rs1057522064
NM_001099922.3(ALG13):c.273A>G (p.Glu91=) rs1057522348
NM_001099922.3(ALG13):c.2754A>G (p.Leu918=) rs1057523456
NM_001099922.3(ALG13):c.2754_2756ACC[10] (p.Pro941_Pro945del) rs750710267
NM_001099922.3(ALG13):c.2754_2756ACC[11] (p.Pro942_Pro945del) rs750710267
NM_001099922.3(ALG13):c.2754_2756ACC[12] (p.Pro943_Pro945del)
NM_001099922.3(ALG13):c.2754_2756ACC[14] (p.Pro945del) rs750710267
NM_001099922.3(ALG13):c.2754_2756ACC[18] (p.Pro943_Pro945dup) rs750710267
NM_001099922.3(ALG13):c.2763A>C (p.Pro921=) rs1602887961
NM_001099922.3(ALG13):c.2769A>C (p.Pro923=) rs1602888164
NM_001099922.3(ALG13):c.2772A>C (p.Pro924=) rs1204623641
NM_001099922.3(ALG13):c.2775A>C (p.Pro925=) rs1285221362
NM_001099922.3(ALG13):c.2778A>C (p.Pro926=) rs1218547242
NM_001099922.3(ALG13):c.2781A>C (p.Pro927=) rs147870070
NM_001099922.3(ALG13):c.2784A>C (p.Pro928=) rs1602888630
NM_001099922.3(ALG13):c.2787A>C (p.Pro929=) rs772431643
NM_001099922.3(ALG13):c.2787A>G (p.Pro929=) rs772431643
NM_001099922.3(ALG13):c.2795C>T (p.Pro932Leu) rs773392173
NM_001099922.3(ALG13):c.2796A>T (p.Pro932=) rs748742452
NM_001099922.3(ALG13):c.2797_2799CCT[10] (p.Pro943_Pro945del) rs56717389
NM_001099922.3(ALG13):c.2797_2799CCT[15] (p.Pro944_Pro945dup) rs56717389
NM_001099922.3(ALG13):c.2797_2799CCT[8] (p.Pro941_Pro945del)
NM_001099922.3(ALG13):c.2797_2799CCT[9] (p.Pro942_Pro945del) rs56717389
NM_001099922.3(ALG13):c.2798_2799insACCACCTCC (p.Pro943_Pro945dup) rs1569522034
NM_001099922.3(ALG13):c.2799T>A (p.Pro933=) rs13440710
NM_001099922.3(ALG13):c.2892A>G (p.Pro964=) rs1556523067
NM_001099922.3(ALG13):c.2933-15G>T rs372767806
NM_001099922.3(ALG13):c.2933-214C>T rs57867104
NM_001099922.3(ALG13):c.2933-57A>G rs138109869
NM_001099922.3(ALG13):c.2973+20T>A rs368694871
NM_001099922.3(ALG13):c.3008A>G (p.Tyr1003Cys) rs201055779
NM_001099922.3(ALG13):c.303C>T (p.Asn101=) rs763113044
NM_001099922.3(ALG13):c.3084C>T (p.Thr1028=) rs758300150
NM_001099922.3(ALG13):c.3093A>G (p.Gln1031=) rs372260338
NM_001099922.3(ALG13):c.3143C>G (p.Ala1048Gly) rs773401427
NM_001099922.3(ALG13):c.3149-12C>T rs1603002604
NM_001099922.3(ALG13):c.3159G>A (p.Pro1053=) rs1556539037
NM_001099922.3(ALG13):c.3221A>G (p.Tyr1074Cys) rs372990620
NM_001099922.3(ALG13):c.3221A>T (p.Tyr1074Phe) rs372990620
NM_001099922.3(ALG13):c.3240A>G (p.Pro1080=) rs773452673
NM_001099922.3(ALG13):c.3252C>G (p.Ser1084=) rs1171897545
NM_001099922.3(ALG13):c.3264T>C (p.Val1088=) rs762647183
NM_001099922.3(ALG13):c.3278C>T (p.Ser1093Phe) rs1465704791
NM_001099922.3(ALG13):c.327G>A (p.Gln109=) rs1602495506
NM_001099922.3(ALG13):c.3312A>G (p.Ala1104=) rs1487734085
NM_001099922.3(ALG13):c.3358A>G (p.Ile1120Val) rs369167525
NM_001099922.3(ALG13):c.3379C>T (p.Pro1127Ser) rs372841179
NM_001099922.3(ALG13):c.3399A>G (p.Val1133=) rs372982045
NM_001099922.3(ALG13):c.3414A>C (p.Ter1138Tyr) rs201820102
NM_001099922.3(ALG13):c.346C>T (p.Leu116=) rs1602495633
NM_001099922.3(ALG13):c.354A>G (p.Lys118=) rs1569510723
NM_001099922.3(ALG13):c.360T>C (p.Gly120=) rs747837898
NM_001099922.3(ALG13):c.371A>G (p.Tyr124Cys) rs145518377
NM_001099922.3(ALG13):c.383+1033G>A rs772039609
NM_001099922.3(ALG13):c.384-5C>T rs763318921
NM_001099922.3(ALG13):c.417T>C (p.Ile139=) rs748326545
NM_001099922.3(ALG13):c.426T>C (p.Ala142=) rs759472632
NM_001099922.3(ALG13):c.42C>A (p.Asp14Glu) rs200293248
NM_001099922.3(ALG13):c.456G>A (p.Leu152=) rs762934062
NM_001099922.3(ALG13):c.474A>G (p.Ser158=) rs1602635527
NM_001099922.3(ALG13):c.486T>C (p.Phe162=) rs751015058
NM_001099922.3(ALG13):c.54G>A (p.Ala18=) rs1406539581
NM_001099922.3(ALG13):c.554T>G (p.Leu185Arg)
NM_001099922.3(ALG13):c.588T>G (p.Pro196=) rs747214832
NM_001099922.3(ALG13):c.638G>A (p.Ser213Asn) rs374748006
NM_001099922.3(ALG13):c.744G>A (p.Ser248=) rs755327837
NM_001099922.3(ALG13):c.751-8_751-6del rs765948340
NM_001099922.3(ALG13):c.81+108C>T rs776511444
NM_001099922.3(ALG13):c.835-264T>G rs16986609
NM_001099922.3(ALG13):c.880C>G (p.Pro294Ala) rs753556936
NM_001099922.3(ALG13):c.886-16C>A rs780688383
NM_001099922.3(ALG13):c.886-17A>G rs1057523046
NM_001099922.3(ALG13):c.886-19A>G rs773121084
NM_001099922.3(ALG13):c.886-7T>C rs1556488604
NM_001099922.3(ALG13):c.975T>G (p.Thr325=) rs767735916

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