List of variants reported as benign for ALG6-congenital disorder of glycosylation 1C

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Total variants: 28

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HGVS	dbSNP	gnomAD frequency
NM_013339.4(ALG6):c.911C>T (p.Ser304Phe)	rs4630153	0.75355
NM_013339.4(ALG6):c.*761T>C	rs3009572	0.60547
NM_013339.4(ALG6):c.494+74A>G	rs6588028	0.59605
NM_013339.4(ALG6):c.347-107A>G	rs1012872	0.35371
NM_013339.4(ALG6):c.-136C>G	rs34542411	0.20075
NM_013339.4(ALG6):c.430-133T>C	rs12755065	0.17545
NM_013339.4(ALG6):c.1058+111T>G	rs4550089	0.16438
NM_013339.4(ALG6):c.981T>C (p.Phe327=)	rs75451833	0.04164
NM_013339.4(ALG6):c.*1322A>G	rs75309742	0.04045
NM_013339.4(ALG6):c.391T>C (p.Tyr131His)	rs35383149	0.02935
NM_013339.4(ALG6):c.*844T>C	rs2884922	0.02393
NM_013339.4(ALG6):c.726C>T (p.Phe242=)	rs59848367	0.02294
NM_013339.4(ALG6):c.678G>T (p.Lys226Asn)	rs35604168	0.01480
NM_013339.4(ALG6):c.1357C>G (p.Leu453Val)	rs41285372	0.01295
NM_013339.4(ALG6):c.1323T>C (p.Tyr441=)	rs116660078	0.00791
NM_013339.4(ALG6):c.751A>G (p.Thr251Ala)	rs61755863	0.00705
NM_013339.4(ALG6):c.1398A>T (p.Leu466=)	rs140158304	0.00167
NM_013339.4(ALG6):c.1452C>T (p.Phe484=)	rs150298974	0.00044
NM_013339.4(ALG6):c.903-13A>G	rs190744579	0.00013
NM_013339.4(ALG6):c.168-17C>G	rs536808870	0.00002
NM_013339.4(ALG6):c.1341C>T (p.Val447=)	rs777326636	0.00001
NM_013339.4(ALG6):c.987+12A>G	rs758406155	0.00001
NM_013339.4(ALG6):c.1327-9dup	rs1236127359
NM_013339.4(ALG6):c.257+10del
NM_013339.4(ALG6):c.346+6dup
NM_013339.4(ALG6):c.681-3del	rs763183173
NM_013339.4(ALG6):c.988-14del
NM_013339.4(ALG6):c.988-8dup	rs779365053

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