ClinVar Miner

List of variants in gene CCNO reported as likely benign by Labcorp Genetics (formerly Invitae), Labcorp

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 70
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HGVS dbSNP gnomAD frequency
NM_021147.5(CCNO):c.1007C>T (p.Pro336Leu) rs115697956 0.00163
NM_021147.5(CCNO):c.134C>A (p.Pro45His) rs139606873 0.00150
NM_021147.5(CCNO):c.107G>A (p.Arg36His) rs142265745 0.00067
NM_021147.5(CCNO):c.1002G>C (p.Met334Ile) rs149215991 0.00056
NM_021147.5(CCNO):c.206A>G (p.Asp69Gly) rs372247606 0.00008
NM_021147.5(CCNO):c.210C>T (p.Gly70=) rs373209105 0.00007
NM_021147.5(CCNO):c.333G>A (p.Ala111=) rs191035273 0.00007
NM_021147.5(CCNO):c.723G>A (p.Thr241=) rs777719468 0.00005
NM_021147.5(CCNO):c.887G>A (p.Arg296Gln) rs761492748 0.00005
NM_021147.5(CCNO):c.579C>T (p.His193=) rs552011098 0.00004
NM_021147.5(CCNO):c.843C>T (p.Ser281=) rs759691847 0.00004
NM_021147.5(CCNO):c.567+10G>A rs755915635 0.00003
NM_021147.5(CCNO):c.837C>A (p.Ser279=) rs569924543 0.00003
NM_021147.5(CCNO):c.999C>T (p.His333=) rs143418535 0.00003
NM_021147.5(CCNO):c.462G>A (p.Leu154=) rs778310459 0.00002
NM_021147.5(CCNO):c.1017C>T (p.Ile339=) rs200969817 0.00001
NM_021147.5(CCNO):c.156G>A (p.Pro52=) rs1359521554 0.00001
NM_021147.5(CCNO):c.183C>T (p.Phe61=) rs760832879 0.00001
NM_021147.5(CCNO):c.30G>A (p.Ser10=) rs771067579 0.00001
NM_021147.5(CCNO):c.567+9G>A rs926256890 0.00001
NM_021147.5(CCNO):c.84G>A (p.Pro28=) rs755568469 0.00001
NM_021147.5(CCNO):c.111C>T (p.Leu37=) rs1745661763
NM_021147.5(CCNO):c.120G>A (p.Lys40=)
NM_021147.5(CCNO):c.135C>T (p.Pro45=) rs2478555919
NM_021147.5(CCNO):c.141C>T (p.Asn47=) rs1580412370
NM_021147.5(CCNO):c.153C>G (p.Leu51=) rs2478555755
NM_021147.5(CCNO):c.156G>T (p.Pro52=) rs1359521554
NM_021147.5(CCNO):c.165C>T (p.Ser55=)
NM_021147.5(CCNO):c.18C>A (p.Pro6=) rs1372192055
NM_021147.5(CCNO):c.198C>T (p.Ser66=)
NM_021147.5(CCNO):c.219C>T (p.Ser73=)
NM_021147.5(CCNO):c.315C>T (p.Cys105=)
NM_021147.5(CCNO):c.327C>A (p.Arg109=) rs1358874292
NM_021147.5(CCNO):c.333G>T (p.Ala111=) rs191035273
NM_021147.5(CCNO):c.336G>A (p.Gln112=)
NM_021147.5(CCNO):c.342C>T (p.Ser114=) rs2111721591
NM_021147.5(CCNO):c.351C>T (p.His117=)
NM_021147.5(CCNO):c.36C>A (p.Pro12=) rs777965356
NM_021147.5(CCNO):c.382-12C>G
NM_021147.5(CCNO):c.382-14C>A rs72749883
NM_021147.5(CCNO):c.382-14C>T rs72749883
NM_021147.5(CCNO):c.382-15C>G rs368489305
NM_021147.5(CCNO):c.382-17C>T
NM_021147.5(CCNO):c.382-4G>A rs2111718851
NM_021147.5(CCNO):c.382-5G>T
NM_021147.5(CCNO):c.382-8C>T rs1488166018
NM_021147.5(CCNO):c.426G>T (p.Pro142=) rs1580411138
NM_021147.5(CCNO):c.435C>T (p.Arg145=) rs1554020005
NM_021147.5(CCNO):c.444C>T (p.Gly148=)
NM_021147.5(CCNO):c.453C>T (p.Phe151=) rs1197167668
NM_021147.5(CCNO):c.460C>T (p.Leu154=) rs2478548531
NM_021147.5(CCNO):c.471G>T (p.Thr157=)
NM_021147.5(CCNO):c.525C>T (p.Phe175=) rs1580410902
NM_021147.5(CCNO):c.528G>A (p.Gln176=)
NM_021147.5(CCNO):c.568-16del rs1438711868
NM_021147.5(CCNO):c.568-4G>C
NM_021147.5(CCNO):c.568-9G>T
NM_021147.5(CCNO):c.630G>T (p.Arg210=) rs2478544655
NM_021147.5(CCNO):c.660G>T (p.Val220=) rs2478544487
NM_021147.5(CCNO):c.663G>A (p.Leu221=)
NM_021147.5(CCNO):c.66C>T (p.Asp22=)
NM_021147.5(CCNO):c.693C>T (p.Pro231=)
NM_021147.5(CCNO):c.705C>T (p.Phe235=)
NM_021147.5(CCNO):c.789G>A (p.Arg263=)
NM_021147.5(CCNO):c.828C>T (p.Thr276=) rs940635330
NM_021147.5(CCNO):c.831C>T (p.Ser277=)
NM_021147.5(CCNO):c.846C>T (p.Leu282=) rs2478542703
NM_021147.5(CCNO):c.93G>A (p.Lys31=)
NM_021147.5(CCNO):c.996T>C (p.Thr332=) rs1210789924
NM_021147.5(CCNO):c.9C>A (p.Thr3=) rs1008454531

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