List of variants in gene ALG13 reported as likely benign for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 98

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HGVS	dbSNP	gnomAD frequency
NM_001099922.3(ALG13):c.2529+275C>T	rs16986620	0.01838
NM_001099922.3(ALG13):c.2933-214C>T	rs57867104	0.01525
NM_001099922.3(ALG13):c.2974-41A>C	rs3027819	0.01497
NM_001099922.3(ALG13):c.835-264T>G	rs16986609	0.01226
NM_001099922.3(ALG13):c.383+2509T>C	rs147964455	0.00772
NM_001099922.3(ALG13):c.2933-57A>G	rs138109869	0.00636
NM_001099922.3(ALG13):c.2530-310G>T	rs142085120	0.00630
NM_001099922.3(ALG13):c.2248-42A>G	rs147250361	0.00623
NM_001099922.3(ALG13):c.1088-55A>G	rs140598403	0.00398
NM_001099922.3(ALG13):c.1501-298G>A	rs183838053	0.00395
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.835-217A>G	rs113803341	0.00274
NM_001099922.3(ALG13):c.2898T>C (p.Tyr966=)	rs368002375	0.00247
NM_001099922.3(ALG13):c.2932+178T>A	rs181510117	0.00229
NM_001099922.3(ALG13):c.2932+179C>A	rs185262155	0.00228
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.3093A>G (p.Gln1031=)	rs372260338	0.00065
NM_001099922.3(ALG13):c.1843C>T (p.Leu615=)	rs374231091	0.00060
NM_001099922.3(ALG13):c.2796A>T (p.Pro932=)	rs748742452	0.00058
NM_001099922.3(ALG13):c.3358A>G (p.Ile1120Val)	rs369167525	0.00058
NM_001099922.3(ALG13):c.3399A>G (p.Val1133=)	rs372982045	0.00047
NM_001099922.3(ALG13):c.2485A>G (p.Met829Val)	rs368075878	0.00046
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.-14G>A	rs199642821	0.00018
NM_001099922.3(ALG13):c.383+1033G>A	rs772039609	0.00017
NM_001099922.3(ALG13):c.2070T>C (p.Asp690=)	rs371239344	0.00014
NM_001099922.3(ALG13):c.2802T>A (p.Pro934=)	rs865879266	0.00014
NM_001099922.3(ALG13):c.1313C>A (p.Thr438Lys)	rs367783946	0.00013
NM_001099922.3(ALG13):c.1747A>G (p.Ile583Val)	rs377397506	0.00013
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.2787A>G (p.Pro929=)	rs772431643	0.00011
NM_001099922.3(ALG13):c.1922A>G (p.His641Arg)	rs766772102	0.00010
NM_001099922.3(ALG13):c.3379C>T (p.Pro1127Ser)	rs372841179	0.00010
NM_001099922.3(ALG13):c.1834C>T (p.Pro612Ser)	rs200516126	0.00009
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.1813G>A (p.Gly605Ser)	rs773666398	0.00007
NM_001099922.3(ALG13):c.288C>T (p.Leu96=)	rs369867857	0.00007
NM_001099922.3(ALG13):c.756T>G (p.Phe252Leu)	rs915629293	0.00007
NM_001099922.3(ALG13):c.108A>G (p.Arg36=)	rs769838471	0.00005
NM_001099922.3(ALG13):c.1377C>G (p.Ala459=)	rs368020541	0.00005
NM_001099922.3(ALG13):c.2213A>G (p.Glu738Gly)	rs374174400	0.00005
NM_001099922.3(ALG13):c.2529+6C>G	rs1569520797	0.00005
NM_001099922.3(ALG13):c.2805T>A (p.Pro935=)	rs754346057	0.00005
NM_001099922.3(ALG13):c.3240A>G (p.Pro1080=)	rs773452673	0.00005
NM_001099922.3(ALG13):c.2013G>A (p.Pro671=)	rs775697727	0.00004
NM_001099922.3(ALG13):c.1798A>G (p.Met600Val)	rs189931917	0.00003
NM_001099922.3(ALG13):c.2401+9G>T	rs1036320277	0.00003
NM_001099922.3(ALG13):c.1977-12C>T	rs374618611	0.00002
NM_001099922.3(ALG13):c.2278G>T (p.Ala760Ser)	rs773286994	0.00002
NM_001099922.3(ALG13):c.2324A>G (p.Lys775Arg)	rs766946325	0.00002
NM_001099922.3(ALG13):c.360T>C (p.Gly120=)	rs747837898	0.00002
NM_001099922.3(ALG13):c.1308A>G (p.Lys436=)	rs1423402192	0.00001
NM_001099922.3(ALG13):c.1869C>T (p.His623=)	rs747208594	0.00001
NM_001099922.3(ALG13):c.1947G>A (p.Pro649=)	rs758659441	0.00001
NM_001099922.3(ALG13):c.426T>C (p.Ala142=)	rs759472632	0.00001
NM_001099922.3(ALG13):c.486T>C (p.Phe162=)	rs751015058	0.00001
NM_001099922.3(ALG13):c.744G>A (p.Ser248=)	rs755327837	0.00001
NM_001099922.3(ALG13):c.1501-199_1501-198del	rs374664795
NM_001099922.3(ALG13):c.2091-8C>G	rs939425312
NM_001099922.3(ALG13):c.2191A>G (p.Thr731Ala)
NM_001099922.3(ALG13):c.2369-214dup	rs755444704
NM_001099922.3(ALG13):c.2380GAA[1] (p.Glu795del)	rs772766102
NM_001099922.3(ALG13):c.2705C>T (p.Ser902Leu)
NM_001099922.3(ALG13):c.2754ACC[10] (p.Pro941_Pro945del)	rs750710267
NM_001099922.3(ALG13):c.2754ACC[14] (p.Pro945del)	rs750710267
NM_001099922.3(ALG13):c.2754ACC[18] (p.Pro943_Pro945dup)	rs750710267
NM_001099922.3(ALG13):c.2763A>C (p.Pro921=)	rs1602887961
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.2793A>T (p.Pro931=)
NM_001099922.3(ALG13):c.2797CCT[10] (p.Pro943_Pro945del)	rs56717389
NM_001099922.3(ALG13):c.2797CCT[11] (p.Pro944_Pro945del)	rs56717389
NM_001099922.3(ALG13):c.2797CCT[14] (p.Pro945dup)	rs56717389
NM_001099922.3(ALG13):c.2797CCT[15] (p.Pro944_Pro945dup)	rs56717389
NM_001099922.3(ALG13):c.2797CCT[8] (p.Pro941_Pro945del)	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.2974-79del	rs75519151
NM_001099922.3(ALG13):c.2974-79dup	rs75519151
NM_001099922.3(ALG13):c.3149-12C>T	rs1603002604
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.327G>A (p.Gln109=)	rs1602495506
NM_001099922.3(ALG13):c.346C>T (p.Leu116=)	rs1602495633
NM_001099922.3(ALG13):c.383+2827A>C
NM_001099922.3(ALG13):c.383+8A>G
NM_001099922.3(ALG13):c.474A>G (p.Ser158=)	rs1602635527
NM_001099922.3(ALG13):c.683G>A (p.Ser228Asn)
NM_001099922.3(ALG13):c.751-8_751-6del	rs765948340
NM_001099922.3(ALG13):c.886-303C>G	rs138878988

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