ClinVar Miner

List of variants in gene MMUT reported as likely pathogenic by Neuberg Centre For Genomic Medicine, NCGM

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000255.4(MMUT):c.571G>A (p.Ala191Thr)	rs1313120333	0.00001
NM_000255.4(MMUT):c.438del (p.Gly145_Tyr146insTer)	rs2481347699

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