List of variants in gene C5 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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: 50

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HGVS	dbSNP	gnomAD frequency
NM_001735.3(C5):c.2059+3A>G	rs374867185	0.00021
NM_001735.3(C5):c.4321G>T (p.Ala1441Ser)	rs143886761	0.00021
NM_001735.3(C5):c.4504+4A>G	rs137867011	0.00014
NM_001735.3(C5):c.4016A>G (p.Glu1339Gly)	rs569871287	0.00013
NM_001735.3(C5):c.1424C>T (p.Ala475Val)	rs151271738	0.00012
NM_001735.3(C5):c.2420C>T (p.Thr807Ile)	rs372326645	0.00011
NM_001735.3(C5):c.3059A>G (p.Tyr1020Cys)	rs768907431	0.00011
NM_001735.3(C5):c.1541C>T (p.Thr514Met)	rs199664327	0.00010
NM_001735.3(C5):c.3732G>A (p.Thr1244=)	rs201280694	0.00010
NM_001735.3(C5):c.3199A>C (p.Ser1067Arg)	rs377417930	0.00009
NM_001735.3(C5):c.4924T>G (p.Leu1642Val)	rs762245967	0.00009
NM_001735.3(C5):c.2653C>T (p.Arg885Cys)	rs373359894	0.00008
NM_001735.3(C5):c.3731C>T (p.Thr1244Met)	rs754562499	0.00007
NM_001735.3(C5):c.1481A>G (p.Asp494Gly)	rs373646644	0.00006
NM_001735.3(C5):c.2033C>T (p.Thr678Met)	rs138509814	0.00006
NM_001735.3(C5):c.3068A>G (p.His1023Arg)	rs760863207	0.00006
NM_001735.3(C5):c.4654G>A (p.Ala1552Thr)	rs147051026	0.00006
NM_001735.3(C5):c.2686G>T (p.Val896Leu)	rs370940275	0.00005
NM_001735.3(C5):c.407C>A (p.Thr136Asn)	rs776192715	0.00005
NM_001735.3(C5):c.4205T>C (p.Ile1402Thr)	rs371503868	0.00005
NM_001735.3(C5):c.116T>C (p.Ile39Thr)	rs1228951703	0.00004
NM_001735.3(C5):c.1816G>A (p.Asp606Asn)	rs775286780	0.00004
NM_001735.3(C5):c.3277G>A (p.Val1093Ile)	rs371131390	0.00004
NM_001735.3(C5):c.1717-5T>C	rs779247145	0.00003
NM_001735.3(C5):c.3413G>A (p.Arg1138Gln)	rs779879112	0.00003
NM_001735.3(C5):c.4127G>A (p.Ser1376Asn)	rs764508773	0.00003
NM_001735.3(C5):c.2177A>G (p.Lys726Arg)	rs369235335	0.00002
NM_001735.3(C5):c.2206A>G (p.Ser736Gly)	rs778780304	0.00002
NM_001735.3(C5):c.2491T>C (p.Tyr831His)	rs1352441352	0.00002
NM_001735.3(C5):c.314A>C (p.Glu105Ala)	rs754822238	0.00002
NM_001735.3(C5):c.4693A>G (p.Ile1565Val)	rs375352964	0.00002
NM_001735.3(C5):c.1358G>A (p.Arg453Gln)	rs768081493	0.00001
NM_001735.3(C5):c.1704C>T (p.Gly568=)	rs758651657	0.00001
NM_001735.3(C5):c.2543A>G (p.Tyr848Cys)	rs1288535384	0.00001
NM_001735.3(C5):c.4081-6A>G	rs563554052	0.00001
NM_001735.3(C5):c.4247C>T (p.Ser1416Leu)	rs148636828	0.00001
NM_001735.3(C5):c.4489G>A (p.Glu1497Lys)	rs376245744	0.00001
NM_001735.3(C5):c.572C>T (p.Pro191Leu)	rs200524363	0.00001
NM_001735.3(C5):c.691A>G (p.Ile231Val)	rs753870842	0.00001
NM_001735.3(C5):c.698C>T (p.Pro233Leu)	rs531284110	0.00001
NM_001735.3(C5):c.975T>A (p.Ile325=)	rs370834994	0.00001
NM_001735.3(C5):c.1759A>T (p.Thr587Ser)	rs2047317447
NM_001735.3(C5):c.2627A>G (p.Gln876Arg)	rs2047128695
NM_001735.3(C5):c.2827A>G (p.Thr943Ala)	rs2047115852
NM_001735.3(C5):c.3676C>T (p.Arg1226Cys)	rs537101618
NM_001735.3(C5):c.4143C>A (p.Ile1381=)	rs150804933
NM_001735.3(C5):c.4652C>T (p.Thr1551Ile)	rs138510251
NM_001735.3(C5):c.4932G>C (p.Trp1644Cys)	rs2131656978
NM_001735.3(C5):c.813A>G (p.Ile271Met)	rs2131788839
NM_001735.3(C5):c.892C>G (p.Gln298Glu)	rs149346283

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