ClinVar Miner

List of variants in gene KNL1 reported as uncertain significance for not specified

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Total variants: 28
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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.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.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.5974G>T (p.Ala1992Ser) rs200052077 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.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.221T>C (p.Met74Thr) rs797045428
NM_144508.5(KNL1):c.5723T>G (p.Leu1908Ter)
NM_144508.5(KNL1):c.5885_5888del (p.Lys1962fs) rs797045429
NM_144508.5(KNL1):c.977C>T (p.Thr326Ile) rs1555420295

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