ClinVar Miner

List of variants in gene ALG13 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 95
Download table as spreadsheet
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.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.1277A>G (p.Asn426Ser) rs1208820400
NM_001099922.3(ALG13):c.1308A>G (p.Lys436=)
NM_001099922.3(ALG13):c.1313C>A (p.Thr438Lys) rs367783946
NM_001099922.3(ALG13):c.1327-19A>G rs375412069
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.1601+11G>A rs770867470
NM_001099922.3(ALG13):c.1729+14A>G rs763484848
NM_001099922.3(ALG13):c.1812C>T (p.Tyr604=) rs768241839
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.1976+20G>A rs1556507692
NM_001099922.3(ALG13):c.1977-12C>T
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
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
NM_001099922.3(ALG13):c.2266A>G (p.Thr756Ala) rs748648454
NM_001099922.3(ALG13):c.2324A>G (p.Lys775Arg)
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
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.2485A>G (p.Met829Val) rs368075878
NM_001099922.3(ALG13):c.2529+275C>T
NM_001099922.3(ALG13):c.2529+6C>G
NM_001099922.3(ALG13):c.2530-310G>T
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.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[14] (p.Pro945del) rs750710267
NM_001099922.3(ALG13):c.2754_2756ACC[18] (p.Pro943_Pro945dup)
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[9] (p.Pro942_Pro945del) rs56717389
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
NM_001099922.3(ALG13):c.2933-57A>G
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.3093A>G (p.Gln1031=) rs372260338
NM_001099922.3(ALG13):c.3143C>G (p.Ala1048Gly) rs773401427
NM_001099922.3(ALG13):c.3149-12C>T
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.3252C>G (p.Ser1084=) rs1171897545
NM_001099922.3(ALG13):c.3278C>T (p.Ser1093Phe) rs1465704791
NM_001099922.3(ALG13):c.3358A>G (p.Ile1120Val) rs369167525
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.360T>C (p.Gly120=) rs747837898
NM_001099922.3(ALG13):c.383+1033G>A rs772039609
NM_001099922.3(ALG13):c.384-5C>T rs763318921
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.486T>C (p.Phe162=) rs751015058
NM_001099922.3(ALG13):c.54G>A (p.Ala18=) rs1406539581
NM_001099922.3(ALG13):c.588T>G (p.Pro196=) rs747214832
NM_001099922.3(ALG13):c.744G>A (p.Ser248=)
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
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

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.