List of variants in gene HCFC1 reported as likely benign by Genetic Services Laboratory, University of Chicago

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_005334.3(HCFC1):c.5859C>T (p.Cys1953=)	rs3027875	0.42119
NM_005334.3(HCFC1):c.2841A>G (p.Pro947=)	rs730106	0.37791
NM_005334.3(HCFC1):c.3490T>C (p.Ser1164Pro)	rs1051152	0.37778
NM_005334.3(HCFC1):c.4185G>A (p.Ala1395=)	rs2071133	0.19260
NM_005334.3(HCFC1):c.4542G>T (p.Leu1514=)	rs3027878	0.16009
NM_005334.3(HCFC1):c.2283C>G (p.Thr761=)	rs2071134	0.15977
NM_005334.3(HCFC1):c.2886G>A (p.Leu962=)	rs3027883	0.05020
NM_005334.3(HCFC1):c.3568G>A (p.Gly1190Ser)	rs185987427	0.01804
NM_005334.3(HCFC1):c.2872A>G (p.Thr958Ala)	rs3027884	0.00091
NM_005334.3(HCFC1):c.4159G>A (p.Val1387Met)	rs200164926	0.00091
NM_005334.3(HCFC1):c.2590G>A (p.Ala864Thr)	rs190023981	0.00075
NM_005334.3(HCFC1):c.2604C>T (p.Ala868=)	rs369241538	0.00038
NM_005334.3(HCFC1):c.3903C>T (p.Thr1301=)	rs375212345	0.00037
NM_005334.3(HCFC1):c.717C>G (p.Thr239=)	rs372516617	0.00031
NM_005334.3(HCFC1):c.2289C>T (p.Pro763=)	rs200081632	0.00015
NM_005334.3(HCFC1):c.4626G>A (p.Glu1542=)	rs372900932	0.00011
NM_005334.3(HCFC1):c.2589C>T (p.Ser863=)	rs375755315	0.00009
NM_005334.3(HCFC1):c.1122C>T (p.Arg374=)	rs781840891	0.00008
NM_005334.3(HCFC1):c.1716G>A (p.Ala572=)	rs371233332	0.00005
NM_005334.3(HCFC1):c.3270C>T (p.Thr1090=)	rs782332238	0.00002
NM_005334.3(HCFC1):c.5517C>T (p.Asp1839=)	rs782063013	0.00002
NM_005334.3(HCFC1):c.1692A>G (p.Ala564=)	rs1557115878	0.00001
NM_005334.3(HCFC1):c.1251C>T (p.Val417=)	rs1557116313
NM_005334.3(HCFC1):c.1461C>T (p.Leu487=)	rs1557116102
NM_005334.3(HCFC1):c.237C>A (p.Pro79=)	rs782481466
NM_005334.3(HCFC1):c.3465G>A (p.Ala1155=)	rs1053320929

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