List of variants reported as benign for 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome

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Total variants: 31

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HGVS	dbSNP	gnomAD frequency
NM_032861.4(SERAC1):c.249C>T (p.Asp83=)	rs6929274	0.71772
NM_032861.4(SERAC1):c.129-34C>G	rs6929520	0.71770
NM_032861.4(SERAC1):c.355+11A>G	rs9356399	0.42562
NM_032861.4(SERAC1):c.1016-11C>T	rs41269577	0.04319
NM_032861.4(SERAC1):c.1403+12G>A	rs117813106	0.02692
NM_032861.4(SERAC1):c.139T>A (p.Phe47Ile)	rs112780453	0.02065
NM_032861.4(SERAC1):c.1293G>A (p.Thr431=)	rs73797641	0.01607
NM_032861.4(SERAC1):c.89T>C (p.Ile30Thr)	rs34270473	0.01029
NM_032861.4(SERAC1):c.739-10T>G	rs118093738	0.00555
NM_032861.4(SERAC1):c.1134C>T (p.Gly378=)	rs116763934	0.00417
NM_032861.4(SERAC1):c.440C>T (p.Thr147Met)	rs114443105	0.00411
NM_032861.4(SERAC1):c.1155A>G (p.Gln385=)	rs116173262	0.00410
NM_032861.4(SERAC1):c.62C>T (p.Pro21Leu)	rs147194699	0.00309
NM_032861.4(SERAC1):c.917G>A (p.Arg306Gln)	rs114943513	0.00253
NM_032861.4(SERAC1):c.1137A>G (p.Val379=)	rs115846131	0.00100
NM_032861.4(SERAC1):c.22G>A (p.Val8Ile)	rs115387731	0.00043
NM_032861.4(SERAC1):c.1659G>A (p.Ser553=)	rs114493681	0.00036
NM_032861.4(SERAC1):c.1308+17C>A	rs201126863	0.00014
NM_032861.4(SERAC1):c.1933C>T (p.Arg645Cys)	rs114624250	0.00010
NM_032861.4(SERAC1):c.487+19C>T	rs372997779	0.00009
NM_032861.4(SERAC1):c.1152C>G (p.Pro384=)	rs201331072	0.00004
NM_032861.4(SERAC1):c.999T>C (p.Ser333=)	rs746668292	0.00004
NM_032861.4(SERAC1):c.266-11A>G	rs574469098	0.00002
NM_032861.4(SERAC1):c.*258G>A
NM_032861.4(SERAC1):c.1016-31_1016-17del	rs374730949
NM_032861.4(SERAC1):c.1309-18_1309-17del	rs780332152
NM_032861.4(SERAC1):c.1396A>T (p.Met466Leu)	rs115459512
NM_032861.4(SERAC1):c.1502-24dup	rs780420200
NM_032861.4(SERAC1):c.266-48dup	rs71027384
NM_032861.4(SERAC1):c.364A>G (p.Ser122Gly)	rs191208250
NM_032861.4(SERAC1):c.92-10del

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