List of variants reported as benign for Developmental and epileptic encephalopathy, 36

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Total variants: 99

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HGVS	dbSNP	gnomAD frequency
NM_001099922.3(ALG13):c.1435+5A>T	rs5985638	0.26139
NM_001099922.3(ALG13):c.1293A>G (p.Pro431=)	rs7063657	0.10892
NM_001099922.3(ALG13):c.1266T>C (p.Gly422=)	rs5985637	0.01375
NM_001099922.3(ALG13):c.183C>T (p.Tyr61=)	rs146925326	0.00950
NM_001099922.3(ALG13):c.2401+12C>A	rs150294098	0.00767
NM_001099922.3(ALG13):c.1152G>A (p.Ala384=)	rs145353928	0.00643
NM_001099922.3(ALG13):c.383+1029A>G	rs139631003	0.00625
NM_001099922.3(ALG13):c.3039A>G (p.Val1013=)	rs183032531	0.00394
NM_001099922.3(ALG13):c.2672C>T (p.Ser891Phe)	rs200066623	0.00390
NM_001099922.3(ALG13):c.2248-4A>G	rs370438099	0.00325
NM_001099922.3(ALG13):c.2799T>A (p.Pro933=)	rs13440710	0.00296
NM_001099922.3(ALG13):c.2898T>C (p.Tyr966=)	rs368002375	0.00247
NM_000032.5(ALAS2):c.1757A>T (p.Tyr586Phe)	rs139596860	0.00189
NM_001099922.3(ALG13):c.2617G>C (p.Ala873Pro)	rs142841538	0.00166
NM_001099922.3(ALG13):c.150C>T (p.Pro50=)	rs147897682	0.00102
NM_001099922.3(ALG13):c.3414A>C (p.Ter1138Tyr)	rs201820102	0.00089
NM_001099922.3(ALG13):c.1591T>C (p.Leu531=)	rs112837367	0.00085
NM_001099922.3(ALG13):c.3093A>G (p.Gln1031=)	rs372260338	0.00065
NM_001099922.3(ALG13):c.1843C>T (p.Leu615=)	rs374231091	0.00060
NM_001099922.3(ALG13):c.3358A>G (p.Ile1120Val)	rs369167525	0.00058
NM_001099922.3(ALG13):c.1327-19A>G	rs375412069	0.00048
NM_001099922.3(ALG13):c.3399A>G (p.Val1133=)	rs372982045	0.00047
NM_001099922.3(ALG13):c.1006-14G>A	rs760527824	0.00045
NM_001099922.3(ALG13):c.638G>A (p.Ser213Asn)	rs374748006	0.00040
NM_001099922.3(ALG13):c.1971G>A (p.Met657Ile)	rs1290639452	0.00039
NM_001099922.3(ALG13):c.2248-15G>C	rs139711892	0.00039
NM_001099922.3(ALG13):c.1729+14A>G	rs763484848	0.00036
NM_001099922.3(ALG13):c.104A>G (p.Asn35Ser)	rs149808406	0.00035
NM_001099922.3(ALG13):c.3008A>G (p.Tyr1003Cys)	rs201055779	0.00024
NM_001099922.3(ALG13):c.886-16C>A	rs780688383	0.00023
NM_001099922.3(ALG13):c.2933-14A>G	rs755886617	0.00021
NM_001099922.3(ALG13):c.2269A>G (p.Met757Val)	rs1451116623	0.00020
NM_001099922.3(ALG13):c.2654T>C (p.Ile885Thr)	rs781459134	0.00015
NM_001099922.3(ALG13):c.2606C>T (p.Ala869Val)	rs138712375	0.00012
NM_001099922.3(ALG13):c.2685C>T (p.His895=)	rs374572450	0.00012
NM_001099922.3(ALG13):c.2309G>A (p.Gly770Glu)	rs751478782	0.00010
NM_001099922.3(ALG13):c.1089T>C (p.Ala363=)	rs760208274	0.00009
NM_001099922.3(ALG13):c.2933-15G>T	rs372767806	0.00008
NM_001099922.3(ALG13):c.384-5C>T	rs763318921	0.00008
NM_001099922.3(ALG13):c.975T>G (p.Thr325=)	rs767735916	0.00008
NM_001099922.3(ALG13):c.288C>T (p.Leu96=)	rs369867857	0.00007
NM_001099922.3(ALG13):c.2369-19T>C	rs376719251	0.00006
NM_001099922.3(ALG13):c.42C>A (p.Asp14Glu)	rs200293248	0.00006
NM_001099922.3(ALG13):c.108A>G (p.Arg36=)	rs769838471	0.00005
NM_001099922.3(ALG13):c.2385A>G (p.Glu795=)	rs759719376	0.00005
NM_001099922.3(ALG13):c.857A>G (p.Lys286Arg)	rs765500818	0.00005
NM_001099922.3(ALG13):c.978T>C (p.Tyr326=)	rs375739139	0.00005
NM_001099922.3(ALG13):c.1435+20A>G	rs368555602	0.00004
NM_001099922.3(ALG13):c.2013G>A (p.Pro671=)	rs775697727	0.00004
NM_001099922.3(ALG13):c.2266A>G (p.Thr756Ala)	rs748648454	0.00004
NM_001099922.3(ALG13):c.2616A>G (p.Gln872=)	rs764400701	0.00004
NM_001099922.3(ALG13):c.3132G>A (p.Ala1044=)	rs376626719	0.00004
NM_001099922.3(ALG13):c.2037A>G (p.Pro679=)	rs764270660	0.00003
NM_001099922.3(ALG13):c.2012C>T (p.Pro671Leu)	rs770150113	0.00002
NM_001099922.3(ALG13):c.2278G>T (p.Ala760Ser)	rs773286994	0.00002
NM_001099922.3(ALG13):c.2369G>A (p.Gly790Glu)	rs745411126	0.00002
NM_001099922.3(ALG13):c.3058A>G (p.Thr1020Ala)	rs3027818	0.00002
NM_001099922.3(ALG13):c.360T>C (p.Gly120=)	rs747837898	0.00002
NM_001099922.3(ALG13):c.378C>T (p.Thr126=)	rs777042118	0.00002
NM_001099922.3(ALG13):c.419C>T (p.Ala140Val)	rs373025706	0.00002
NM_001099922.3(ALG13):c.995A>G (p.Tyr332Cys)	rs370098098	0.00002
NM_001099922.3(ALG13):c.1064A>G (p.Gln355Arg)	rs372521943	0.00001
NM_001099922.3(ALG13):c.1641A>G (p.Gln547=)	rs768589790	0.00001
NM_001099922.3(ALG13):c.2573A>G (p.Asn858Ser)	rs756238772	0.00001
NM_001099922.3(ALG13):c.2932+17A>G	rs760993782	0.00001
NM_001099922.3(ALG13):c.486T>C (p.Phe162=)	rs751015058	0.00001
NM_001099922.3(ALG13):c.1186A>C (p.Arg396=)
NM_001099922.3(ALG13):c.1250+8del	rs2148114059
NM_001099922.3(ALG13):c.1601+11G>A	rs770867470
NM_001099922.3(ALG13):c.1818G>A (p.Lys606=)
NM_001099922.3(ALG13):c.2145T>C (p.Tyr715=)
NM_001099922.3(ALG13):c.2248-14TC[2]	rs746217514
NM_001099922.3(ALG13):c.2338T>G (p.Leu780Val)
NM_001099922.3(ALG13):c.2380GAA[1] (p.Glu795del)	rs772766102
NM_001099922.3(ALG13):c.2457+15_2457+17del	rs761459857
NM_001099922.3(ALG13):c.2457+16T>C
NM_001099922.3(ALG13):c.2457+17A>C
NM_001099922.3(ALG13):c.2752_2753insACC (p.Ser917_Leu918insHis)
NM_001099922.3(ALG13):c.2754ACC[13] (p.Pro944_Pro945del)	rs750710267
NM_001099922.3(ALG13):c.2754ACC[17] (p.Pro944_Pro945dup)	rs750710267
NM_001099922.3(ALG13):c.2795_2796insCCT (p.Pro932_Pro933insLeu)
NM_001099922.3(ALG13):c.2797CCT[11] (p.Pro944_Pro945del)	rs56717389
NM_001099922.3(ALG13):c.2797CCT[12] (p.Pro945del)	rs56717389
NM_001099922.3(ALG13):c.2797CCT[14] (p.Pro945dup)	rs56717389
NM_001099922.3(ALG13):c.2797CCT[9] (p.Pro942_Pro945del)	rs56717389
NM_001099922.3(ALG13):c.2798_2799insACCTCC (p.Pro944_Pro945dup)	rs1569522034
NM_001099922.3(ALG13):c.2860A>G (p.Asn954Asp)
NM_001099922.3(ALG13):c.288C>G (p.Leu96=)
NM_001099922.3(ALG13):c.2974-7G>T
NM_001099922.3(ALG13):c.2987G>A (p.Ser996Asn)
NM_001099922.3(ALG13):c.3221A>G (p.Tyr1074Cys)	rs372990620
NM_001099922.3(ALG13):c.3343A>G (p.Ile1115Val)
NM_001099922.3(ALG13):c.383+2786C>T
NM_001099922.3(ALG13):c.383+8A>G
NM_001099922.3(ALG13):c.751-8_751-6del	rs765948340
NM_001099922.3(ALG13):c.801A>G (p.Ser267=)
NM_001099922.3(ALG13):c.82-10C>T
NM_001099922.3(ALG13):c.834+14A>G
NM_001099922.3(ALG13):c.880C>T (p.Pro294Ser)	rs753556936

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