List of variants in gene MLC1 reported as not provided

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

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_015166.4(MLC1):c.278C>T (p.Ser93Leu)	rs80358245	0.00001
NM_015166.4(MLC1):c.925C>A (p.Leu309Met)	rs80358240	0.00001
NM_015166.4(MLC1):c.135dup (p.Cys46fs)	rs80358241
NM_015166.4(MLC1):c.176G>A (p.Gly59Glu)	rs80358242
NM_015166.4(MLC1):c.298_423+108del	rs1555967644
NM_015166.4(MLC1):c.353C>G (p.Thr118Arg)	rs281875316
NM_015166.4(MLC1):c.373T>C (p.Cys125Arg)	rs281875314
NM_015166.4(MLC1):c.634G>A (p.Gly212Arg)	rs281875317
NM_015166.4(MLC1):c.733G>C (p.Ala245Pro)	rs281875312
NM_015166.4(MLC1):c.736A>C (p.Ser246Arg)	rs281875315
NM_015166.4(MLC1):c.824C>A (p.Ala275Asp)	rs764669598
NM_015166.4(MLC1):c.908_918delinsGCA (p.Val303fs)	rs2146772952
NM_015166.4(MLC1):c.959C>A (p.Thr320Lys)	rs281875313

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