List of variants in gene TUFM reported as benign for Combined oxidative phosphorylation defect type 4

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_003321.5(TUFM):c.817+13T>C	rs4788099	0.34806
NM_003321.5(TUFM):c.922+29C>G	rs61737565	0.34806
NM_003321.5(TUFM):c.*300T>G	rs3088215	0.34801
NM_003321.5(TUFM):c.248-18G>A	rs8061877	0.24423
NM_003321.5(TUFM):c.198C>T (p.Ile66=)	rs11542257	0.02831
NM_003321.5(TUFM):c.*24C>T	rs8754	0.02648
NM_003321.5(TUFM):c.520-8A>T	rs145900455	0.00116

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