ClinVar Miner

List of variants in gene ALG13 studied for History of neurodevelopmental disorder

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Total variants: 25
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HGVS dbSNP
NM_001099922.3(ALG13):c.104A>G (p.Asn35Ser) rs149808406
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.1211A>C (p.Glu404Ala) rs1569517608
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.13T>C (p.Phe5Leu) rs199754211
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.1831C>G (p.Leu611Val) rs199505558
NM_001099922.3(ALG13):c.183C>T (p.Tyr61=) rs146925326
NM_001099922.3(ALG13):c.2248-4A>G rs370438099
NM_001099922.3(ALG13):c.245-4G>T rs761270344
NM_001099922.3(ALG13):c.2573A>G (p.Asn858Ser) rs756238772
NM_001099922.3(ALG13):c.2617G>C (p.Ala873Pro) rs142841538
NM_001099922.3(ALG13):c.2672C>T (p.Ser891Phe) rs200066623
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.3240A>G (p.Pro1080=) rs773452673
NM_001099922.3(ALG13):c.3312A>G (p.Ala1104=) rs1487734085
NM_001099922.3(ALG13):c.354A>G (p.Lys118=) rs1569510723
NM_001099922.3(ALG13):c.756T>G (p.Phe252Leu) rs915629293
NM_001099922.3(ALG13):c.880C>G (p.Pro294Ala) rs753556936
NM_001099922.3(ALG13):c.975T>G (p.Thr325=) rs767735916

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