List of variants in gene MFN2 reported as uncertain significance by Illumina Laboratory Services, Illumina

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: 47

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HGVS	dbSNP	gnomAD frequency
NM_014874.4(MFN2):c.756C>T (p.Asn252=)	rs137960129	0.00053
NM_014874.4(MFN2):c.1827C>T (p.Ser609=)	rs138724074	0.00039
NM_014874.4(MFN2):c.*413C>T	rs558887681	0.00031
NM_014874.4(MFN2):c.*1054C>T	rs951038336	0.00025
NM_014874.4(MFN2):c.*1539G>A	rs557643473	0.00025
NM_014874.4(MFN2):c.*1535C>T	rs778755558	0.00021
NM_014874.4(MFN2):c.*946C>A	rs765105334	0.00019
NM_014874.4(MFN2):c.2157G>A (p.Lys719=)	rs148441213	0.00017
NM_014874.4(MFN2):c.1794_1796del	rs540280019	0.00016
NM_014874.4(MFN2):c.*1276G>A	rs766342161	0.00014
NM_014874.4(MFN2):c.*256G>A	rs557772799	0.00012
NM_014874.4(MFN2):c.*1153C>T	rs542684406	0.00011
NM_014874.4(MFN2):c.*36G>A	rs377468070	0.00011
NM_014874.4(MFN2):c.1987C>T (p.Arg663Cys)	rs369762154	0.00011
NM_014874.4(MFN2):c.*813G>A	rs771869272	0.00010
NM_014874.4(MFN2):c.842G>C (p.Cys281Ser)	rs147136530	0.00010
NM_014874.4(MFN2):c.*1295G>A	rs763783578	0.00005
NM_014874.4(MFN2):c.1269G>A (p.Thr423=)	rs145994616	0.00004
NM_014874.4(MFN2):c.*1662T>C	rs1020801224	0.00003
NM_014874.4(MFN2):c.*297T>A	rs886045224	0.00003
NM_014874.4(MFN2):c.2145C>T (p.Ala715=)	rs571011689	0.00003
NM_014874.4(MFN2):c.*1222G>A	rs531732785	0.00001
NM_014874.4(MFN2):c.*131G>A	rs1639706861	0.00001
NM_014874.4(MFN2):c.*1902C>T	rs933126234	0.00001
NM_014874.4(MFN2):c.*870C>T	rs886045227	0.00001
NM_014874.4(MFN2):c.2204+13C>T	rs200441797	0.00001
NM_014874.3(MFN2):c.-217C>A	rs886045218
NM_014874.4(MFN2):c.*1068C>T	rs886045229
NM_014874.4(MFN2):c.*121A>G	rs886045222
NM_014874.4(MFN2):c.*1392A>G	rs886045230
NM_014874.4(MFN2):c.*1640del	rs35943162
NM_014874.4(MFN2):c.*1640dup	rs35943162
NM_014874.4(MFN2):c.*1763G>A	rs1639769422
NM_014874.4(MFN2):c.*1797GTT[1]	rs140537612
NM_014874.4(MFN2):c.*381C>A	rs966318629
NM_014874.4(MFN2):c.*57C>T	rs886045221
NM_014874.4(MFN2):c.*610del	rs747291228
NM_014874.4(MFN2):c.*864T>C	rs886045226
NM_014874.4(MFN2):c.*935G>T	rs886045228
NM_014874.4(MFN2):c.1436C>G (p.Ser479Cys)	rs1639333679
NM_014874.4(MFN2):c.153G>T (p.Gln51His)	rs886045219
NM_014874.4(MFN2):c.1631A>G (p.His544Arg)	rs1639384043
NM_014874.4(MFN2):c.1938C>A (p.Val646=)	rs1040702840
NM_014874.4(MFN2):c.2211A>G (p.Lys737=)	rs1639694970
NM_014874.4(MFN2):c.271G>A (p.Val91Met)	rs1557519001
NM_014874.4(MFN2):c.708G>A (p.Thr236=)	rs1557524867
NM_014874.4(MFN2):c.898C>T (p.Arg300Cys)	rs863224066

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