List of variants in gene FOXRED1 reported as uncertain significance for mitochondrial complex 1 deficiency, nuclear type 19

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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_017547.4(FOXRED1):c.1261G>A (p.Val421Met)	rs199542988	0.00004
NM_017547.4(FOXRED1):c.943A>G (p.Thr315Ala)	rs111338847	0.00001
NM_017547.4(FOXRED1):c.1234_1239del (p.Asp412_Tyr413del)
NM_017547.4(FOXRED1):c.1418G>A (p.Arg473His)
NM_017547.4(FOXRED1):c.354G>C (p.Gln118His)
NM_017547.4(FOXRED1):c.449T>G (p.Leu150Arg)	rs756631739
NM_017547.4(FOXRED1):c.632G>C (p.Gly211Ala)	rs536400690
NM_017547.4(FOXRED1):c.677G>A (p.Gly226Glu)
NM_017547.4(FOXRED1):c.682C>T (p.Arg228Trp)	rs758966293
NM_017547.4(FOXRED1):c.972-3C>A	rs781102596

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