List of variants in gene FLVCR2 reported as uncertain significance for cerebellar disorder

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: 42

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HGVS	dbSNP	gnomAD frequency
NM_017791.3(FLVCR2):c.*756A>G	rs78654241	0.00279
NM_017791.3(FLVCR2):c.*18C>T	rs369026585	0.00059
NM_017791.3(FLVCR2):c.*1070T>C	rs533763314	0.00039
NM_017791.3(FLVCR2):c.*1071G>T	rs553617789	0.00039
NM_017791.3(FLVCR2):c.421G>A (p.Val141Met)	rs193042691	0.00028
NM_017791.3(FLVCR2):c.*155C>T	rs562468033	0.00019
NM_017791.3(FLVCR2):c.286A>G (p.Met96Val)	rs199805789	0.00018
NM_017791.3(FLVCR2):c.*1633A>C	rs552943781	0.00016
NM_017791.3(FLVCR2):c.953-15C>T	rs188707531	0.00016
NM_017791.3(FLVCR2):c.*675A>G	rs1025714059	0.00010
NM_017791.3(FLVCR2):c.*510A>G	rs182904017	0.00009
NM_017791.3(FLVCR2):c.766A>G (p.Ile256Val)	rs559975316	0.00005
NM_017791.3(FLVCR2):c.*1588A>C	rs764448107	0.00004
NM_017791.3(FLVCR2):c.*1672G>A	rs569521792	0.00004
NM_017791.3(FLVCR2):c.164C>T (p.Pro55Leu)	rs372243784	0.00004
NM_017791.3(FLVCR2):c.1278T>C (p.Ala426=)	rs762529599	0.00002
NM_017791.3(FLVCR2):c.*893T>C	rs1890444124	0.00001
NM_017791.3(FLVCR2):c.*952T>G	rs747845375	0.00001
NM_017791.3(FLVCR2):c.1157_1158del (p.Leu386fs)	rs779784201	0.00001
NM_017791.3(FLVCR2):c.1474C>T (p.Arg492Trp)	rs139495418	0.00001
NM_017791.3(FLVCR2):c.277T>C (p.Cys93Arg)	rs767398242	0.00001
NM_017791.3(FLVCR2):c.329_334del (p.Asn110_Phe112delinsIle)	rs746459536	0.00001
NM_017791.3(FLVCR2):c.604G>A (p.Ala202Thr)	rs886050786	0.00001
NM_017791.3(FLVCR2):c.69G>A (p.Ala23=)	rs1888525051	0.00001
NM_017791.3(FLVCR2):c.78C>A (p.Ser26Arg)	rs768707435	0.00001
NM_017791.3(FLVCR2):c.839C>G (p.Pro280Arg)	rs267606823	0.00001
NM_017791.3(FLVCR2):c.947C>G (p.Thr316Ser)	rs779117746	0.00001
NM_017791.3(FLVCR2):c.*1003G>A	rs549464206
NM_017791.3(FLVCR2):c.*1322G>A	rs1566800405
NM_017791.3(FLVCR2):c.*1613C>T	rs1890460668
NM_017791.3(FLVCR2):c.*379T>C	rs886050789
NM_017791.3(FLVCR2):c.*513A>G	rs1890435742
NM_017791.3(FLVCR2):c.*517C>T	rs188459017
NM_017791.3(FLVCR2):c.*644G>A	rs1890438951
NM_017791.3(FLVCR2):c.*856T>C	rs1890443552
NM_017791.3(FLVCR2):c.*98T>C	rs886050788
NM_017791.3(FLVCR2):c.1326C>T (p.Leu442=)	rs886050787
NM_017791.3(FLVCR2):c.1580G>T (p.Ter527Leu)	rs1566799791
NM_017791.3(FLVCR2):c.1581A>C (p.Ter527Cys)	rs1566799795
NM_017791.3(FLVCR2):c.360C>G (p.Ala120=)	rs906645811
NM_017791.3(FLVCR2):c.669+8G>C	rs769337002
NM_017791.3(FLVCR2):c.998G>A (p.Arg333His)	rs757778790

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