List of variants in gene MMAA reported as not provided for nutritional disorder

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_172250.3(MMAA):c.433C>T (p.Arg145Ter)	rs104893851	0.00017
NM_172250.3(MMAA):c.266T>C (p.Leu89Pro)	rs864309726	0.00002
NM_172250.3(MMAA):c.1076G>A (p.Arg359Gln)	rs864309731	0.00001
NM_172250.3(MMAA):c.283C>T (p.Gln95Ter)	rs104893846	0.00001
NM_172250.3(MMAA):c.64C>T (p.Arg22Ter)	rs765799472	0.00001
NM_172250.3(MMAA):c.733+1G>A	rs779939886	0.00001
NM_172250.3(MMAA):c.988C>T (p.Arg330Ter)	rs571038432	0.00001
NM_172250.3(MMAA):c.161G>A (p.Trp54Ter)	rs864309725
NM_172250.3(MMAA):c.358C>T (p.Gln120Ter)	rs864309727
NM_172250.3(MMAA):c.370C>T (p.Gln124Ter)	rs796064514
NM_172250.3(MMAA):c.397C>T (p.Gln133Ter)	rs754545360
NM_172250.3(MMAA):c.503del (p.Thr168fs)	rs864309728
NM_172250.3(MMAA):c.562G>C (p.Gly188Arg)	rs864309729
NM_172250.3(MMAA):c.593_596del (p.Thr198fs)	rs796051993
NM_172250.3(MMAA):c.650T>A (p.Leu217Ter)	rs140356252
NM_172250.3(MMAA):c.653G>A (p.Gly218Glu)	rs864309730

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