List of variants in gene MSTO1 reported as likely pathogenic for hereditary skeletal muscle disorder

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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: 10

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HGVS	dbSNP	gnomAD frequency
NM_018116.4(MSTO1):c.706G>C (p.Asp236His)	rs753488873	0.00013
NM_018116.4(MSTO1):c.651C>G (p.Phe217Leu)	rs776826330	0.00012
NM_018116.4(MSTO1):c.836G>A (p.Arg279His)	rs563943670	0.00008
NM_018116.4(MSTO1):c.22G>A (p.Val8Met)	rs762798018	0.00005
NM_018116.4(MSTO1):c.887_888del (p.Leu296fs)	rs752022363	0.00004
NM_018116.4(MSTO1):c.971C>T (p.Thr324Ile)	rs622288	0.00004
NM_018116.4(MSTO1):c.1259del (p.Gly420fs)	rs1248439783
NM_018116.4(MSTO1):c.676C>T (p.Gln226Ter)	rs1208636573
NM_018116.4(MSTO1):c.716C>A (p.Ser239Tyr)
NM_018116.4(MSTO1):c.767G>A (p.Arg256Gln)

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