List of variants in gene MLC1 reported as benign for Megalencephalic leukoencephalopathy with subcortical cysts

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_015166.4(MLC1):c.895-259G>A	rs8142282	0.49774
NM_015166.4(MLC1):c.895-9C>T	rs11568185	0.11704
NM_015166.4(MLC1):c.597A>G (p.Ser199=)	rs6010164	0.11147
NM_015166.4(MLC1):c.594C>T (p.Tyr198=)	rs6010165	0.11145
NM_015166.4(MLC1):c.978C>T (p.Cys326=)	rs11568186	0.10918
NM_015166.4(MLC1):c.996T>C (p.Ser332=)	rs11568187	0.10904
NM_015166.4(MLC1):c.512G>T (p.Cys171Phe)	rs6010260	0.10037
NM_015166.4(MLC1):c.895-261A>G	rs8136173	0.09460
NM_015166.4(MLC1):c.1031A>G (p.Asn344Ser)	rs11568188	0.09405
NM_015166.4(MLC1):c.-59-17T>C	rs9628323	0.03393
NM_015166.4(MLC1):c.279G>A (p.Ser93=)	rs11568172	0.00422
NM_015166.4(MLC1):c.628G>A (p.Val210Ile)	rs11568178	0.00110
NM_015166.4(MLC1):c.627C>T (p.Ala209=)	rs138153307	0.00071
NM_015166.4(MLC1):c.601G>A (p.Val201Ile)	rs147572634	0.00063
NM_015166.4(MLC1):c.544G>A (p.Ala182Thr)	rs537457768	0.00002
NM_015166.3(MLC1):c.-528dup	rs137931
NM_015166.4(MLC1):c.1052_1053insCGGGGAGGTGAGTGGCCTGTGGGGTGGGGGTGC (p.Val354_Ala355insSerGlyLeuTrpGlyGlyGlyAlaGlyGluVal)	rs745656804

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