ClinVar Miner

List of variants in gene ALG13 reported as benign

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Total variants: 47
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HGVS dbSNP
NM_001099922.3(ALG13):c.1064A>G (p.Gln355Arg) rs372521943
NM_001099922.3(ALG13):c.108A>G (p.Arg36=) rs769838471
NM_001099922.3(ALG13):c.1152G>A (p.Ala384=) rs145353928
NM_001099922.3(ALG13):c.1266T>C (p.Gly422=) rs5985637
NM_001099922.3(ALG13):c.1293A>G (p.Pro431=) rs7063657
NM_001099922.3(ALG13):c.1435+5A>T rs5985638
NM_001099922.3(ALG13):c.1591T>C (p.Leu531=) rs112837367
NM_001099922.3(ALG13):c.1641A>G (p.Gln547=) rs768589790
NM_001099922.3(ALG13):c.183C>T (p.Tyr61=) rs146925326
NM_001099922.3(ALG13):c.1843C>T (p.Leu615=) rs374231091
NM_001099922.3(ALG13):c.2012C>T (p.Pro671Leu) rs770150113
NM_001099922.3(ALG13):c.2013G>A (p.Pro671=) rs775697727
NM_001099922.3(ALG13):c.2248-4A>G rs370438099
NM_001099922.3(ALG13):c.2269A>G (p.Met757Val) rs1451116623
NM_001099922.3(ALG13):c.2278G>T (p.Ala760Ser) rs773286994
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.2401+12C>A rs150294098
NM_001099922.3(ALG13):c.2530-262C>T rs7055116
NM_001099922.3(ALG13):c.2573A>G (p.Asn858Ser) rs756238772
NM_001099922.3(ALG13):c.2606C>T (p.Ala869Val) rs138712375
NM_001099922.3(ALG13):c.2616A>G (p.Gln872=) rs764400701
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.2672C>T (p.Ser891Phe) rs200066623
NM_001099922.3(ALG13):c.2754_2756ACC[13] (p.Pro944_Pro945del) rs750710267
NM_001099922.3(ALG13):c.2754_2756ACC[17] (p.Pro944_Pro945dup) rs750710267
NM_001099922.3(ALG13):c.2797_2799CCT[11] (p.Pro944_Pro945del) rs56717389
NM_001099922.3(ALG13):c.2797_2799CCT[12] (p.Pro945del) rs56717389
NM_001099922.3(ALG13):c.2797_2799CCT[9] (p.Pro942_Pro945del) rs56717389
NM_001099922.3(ALG13):c.2798_2799insACCTCC (p.Pro944_Pro945dup)
NM_001099922.3(ALG13):c.2898T>C (p.Tyr966=) rs368002375
NM_001099922.3(ALG13):c.3008A>G (p.Tyr1003Cys) rs201055779
NM_001099922.3(ALG13):c.3039A>G (p.Val1013=) rs183032531
NM_001099922.3(ALG13):c.3058A>G (p.Thr1020Ala) rs3027818
NM_001099922.3(ALG13):c.3093A>G (p.Gln1031=) rs372260338
NM_001099922.3(ALG13):c.3132G>A (p.Ala1044=) rs376626719
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+1029A>G rs139631003
NM_001099922.3(ALG13):c.384-5C>T rs763318921
NM_001099922.3(ALG13):c.638G>A (p.Ser213Asn) rs374748006
NM_001099922.3(ALG13):c.857A>G (p.Lys286Arg) rs765500818
NM_001099922.3(ALG13):c.975T>G (p.Thr325=) rs767735916
NM_001099922.3(ALG13):c.995A>G (p.Tyr332Cys) rs370098098

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