List of variants reported as uncertain significance for Combined oxidative phosphorylation defect type 11 by Fulgent Genetics, Fulgent Genetics

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Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_017909.4(RMND1):c.795C>G (p.His265Gln)	rs150706976	0.00060
NM_017909.4(RMND1):c.260G>A (p.Arg87His)	rs142059662	0.00011
NM_017909.4(RMND1):c.257C>T (p.Ala86Val)	rs746842151	0.00006
NM_017909.4(RMND1):c.1084C>T (p.Arg362Cys)	rs755188314	0.00004
NM_017909.4(RMND1):c.526T>A (p.Phe176Ile)	rs562882988	0.00004
NM_017909.4(RMND1):c.68G>A (p.Arg23Gln)	rs377114459	0.00004
NM_017909.4(RMND1):c.188A>G (p.Asn63Ser)	rs374223733	0.00003
NM_017909.4(RMND1):c.661G>C (p.Gly221Arg)	rs1275538949	0.00003
NM_017909.4(RMND1):c.920A>G (p.Asn307Ser)	rs746632175	0.00002
NM_017909.4(RMND1):c.1289G>C (p.Trp430Ser)	rs755793918	0.00001
NM_017909.4(RMND1):c.1159G>C (p.Asp387His)	rs372096369
NM_017909.4(RMND1):c.1295T>C (p.Ile432Thr)	rs1411929426

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