List of variants in gene KNL1 reported as uncertain significance 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: 38

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HGVS	dbSNP	gnomAD frequency
NM_144508.5(KNL1):c.5271C>T (p.Cys1757=)	rs191249840	0.00173
NM_144508.5(KNL1):c.4379T>C (p.Ile1460Thr)	rs187007187	0.00162
NM_144508.5(KNL1):c.2311G>A (p.Val771Ile)	rs151288115	0.00107
NM_144508.5(KNL1):c.251-7T>A	rs555296963	0.00106
NM_144508.5(KNL1):c.4231G>A (p.Gly1411Arg)	rs150569450	0.00103
NM_144508.5(KNL1):c.6482A>G (p.Asp2161Gly)	rs142872154	0.00097
NM_144508.5(KNL1):c.5522G>A (p.Arg1841His)	rs201880719	0.00088
NM_144508.5(KNL1):c.1970C>T (p.Pro657Leu)	rs199767066	0.00083
NM_144508.5(KNL1):c.2268A>G (p.Ser756=)	rs202012571	0.00073
NM_144508.5(KNL1):c.251-9T>C	rs371294019	0.00066
NM_144508.5(KNL1):c.4615G>A (p.Ala1539Thr)	rs199770734	0.00064
NM_144508.5(KNL1):c.4340C>T (p.Thr1447Ile)	rs200605040	0.00056
NM_144508.5(KNL1):c.2815A>T (p.Met939Leu)	rs145740834	0.00045
NM_144508.5(KNL1):c.3749C>T (p.Ala1250Val)	rs115132152	0.00034
NM_144508.5(KNL1):c.5974G>T (p.Ala1992Ser)	rs200052077	0.00014
NM_144508.5(KNL1):c.89C>T (p.Pro30Leu)	rs200234622	0.00014
NM_144508.5(KNL1):c.6284A>G (p.Asn2095Ser)	rs371898340	0.00010
NM_144508.5(KNL1):c.910C>T (p.Arg304Trp)	rs750955272	0.00010
NM_144508.5(KNL1):c.1768G>T (p.Ala590Ser)	rs201334214	0.00006
NM_144508.5(KNL1):c.3474A>G (p.Thr1158=)	rs774901560	0.00006
NM_144508.5(KNL1):c.6164C>T (p.Ala2055Val)	rs375595681	0.00006
NM_144508.5(KNL1):c.6172+5T>C	rs769654305	0.00006
NM_144508.5(KNL1):c.6425C>T (p.Pro2142Leu)	rs202196865	0.00006
NM_144508.5(KNL1):c.6796C>G (p.Pro2266Ala)	rs536166099	0.00004
NM_144508.5(KNL1):c.6334G>A (p.Val2112Ile)	rs377578399	0.00003
NM_144508.5(KNL1):c.905A>C (p.Asn302Thr)	rs573778696	0.00003
NM_144508.5(KNL1):c.3633C>T (p.Ile1211=)	rs374543266	0.00002
NM_144508.5(KNL1):c.1336A>G (p.Met446Val)	rs540961321	0.00001
NM_144508.5(KNL1):c.3517T>G (p.Phe1173Val)	rs373188974	0.00001
NM_144508.5(KNL1):c.3706G>T (p.Ala1236Ser)	rs775377691	0.00001
NM_144508.5(KNL1):c.4382A>T (p.Asn1461Ile)	rs1156447715	0.00001
NM_144508.5(KNL1):c.-2_1del (p.Met1del)	rs587780292
NM_144508.5(KNL1):c.221T>C (p.Met74Thr)	rs797045428
NM_144508.5(KNL1):c.253A>G (p.Thr85Ala)	rs566292216
NM_144508.5(KNL1):c.2784T>C (p.Thr928=)	rs587780293
NM_144508.5(KNL1):c.5885_5888del (p.Lys1962fs)	rs797045429
NM_144508.5(KNL1):c.6094+4_6094+8del	rs587780294
NM_144508.5(KNL1):c.977C>T (p.Thr326Ile)	rs1555420295

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