"PreventionGenetics, part of Exact Sciences"[submitter] AND "MICU1"[ge - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1668411	NM_001195518.2(MICU1):c.653-8C>T	MICU1	Single nucleotide variant (intron variant)	MICU1-related disorder +1 more	GBenign/Likely benign
Select item 2631843	NM_001195518.2(MICU1):c.553C>T (p.Arg185Ter)	MICU1 (R185* +2 more)	Single nucleotide variant (nonsense +1 more)	MICU1-related disorder	GLikely pathogenic
Select item 1583449	NM_001195518.2(MICU1):c.420T>C (p.Pro140=)	MICU1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign

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