List of variants reported as pathogenic for nutritional disorder by University Children's Hospital, University of Zurich

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Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_172250.3(MMAA):c.658G>A (p.Val220Met)	rs150376474	0.00003
NM_172250.3(MMAA):c.651dup (p.Gly218fs)	rs1314623572	0.00001
NM_172250.3(MMAA):c.733+1G>A	rs779939886	0.00001
NM_172250.3(MMAA):c.1034del (p.Phe345fs)	rs398124552
NM_172250.3(MMAA):c.1196_1197delinsTT (p.Gly399Val)	rs1553959152
NM_172250.3(MMAA):c.202C>T (p.Gln68Ter)	rs754894257
NM_172250.3(MMAA):c.267_268del (p.Thr91fs)	rs1553957906
NM_172250.3(MMAA):c.290_296del (p.Gln97fs)	rs1553957907
NM_172250.3(MMAA):c.298_312del (p.Cys100_Ala104del)	rs780082584
NM_172250.3(MMAA):c.441dup (p.Leu148fs)	rs1553958126
NM_172250.3(MMAA):c.455del (p.Pro152fs)	rs1553958127
NM_172250.3(MMAA):c.527_528del (p.Val176fs)	rs1553958158
NM_172250.3(MMAA):c.575G>A (p.Gly192Asp)	rs1553958392
NM_172250.3(MMAA):c.721A>T (p.Ile241Phe)	rs756221585
NM_172250.3(MMAA):c.728C>A (p.Thr243Asn)	rs1553958417
NM_172250.3(MMAA):c.72C>A (p.Tyr24Ter)	rs1553957883
NM_172250.3(MMAA):c.820-1G>A	rs1553959017
NM_172250.3(MMAA):c.860C>A (p.Ala287Asp)	rs1553959024
NM_172250.3(MMAA):c.875A>T (p.Asp292Val)	rs1553959025

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