List of variants reported as likely pathogenic for megalencephalic leukoencephalopathy with subcortical cysts by Myriad Genetics, Inc.

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_015166.4(MLC1):c.178-10T>A	rs80358243	0.00001
NM_015166.4(MLC1):c.278C>T (p.Ser93Leu)	rs80358245	0.00001
NM_015166.4(MLC1):c.176G>A (p.Gly59Glu)	rs80358242
NM_015166.4(MLC1):c.341T>A (p.Leu114Ter)	rs1458824689
NM_015166.4(MLC1):c.377T>A (p.Leu126Ter)	rs2062078281
NM_015166.4(MLC1):c.383G>A (p.Trp128Ter)
NM_015166.4(MLC1):c.393C>A (p.Cys131Ter)	rs2062077684
NM_015166.4(MLC1):c.413C>A (p.Ser138Ter)	rs2062076867
NM_015166.4(MLC1):c.517A>T (p.Lys173Ter)	rs766461175
NM_015166.4(MLC1):c.559G>T (p.Glu187Ter)	rs761502278
NM_015166.4(MLC1):c.592del (p.Tyr198fs)
NM_015166.4(MLC1):c.596C>G (p.Ser199Ter)
NM_015166.4(MLC1):c.683_684insAATACTTTGA (p.Leu228_Ser229insIleLeuTer)
NM_015166.4(MLC1):c.839C>A (p.Ser280Ter)	rs121908341
NM_015166.4(MLC1):c.848del (p.Ile283fs)
NM_015166.4(MLC1):c.892A>T (p.Lys298Ter)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.