ClinVar Miner

List of variants in gene KCNC3 reported by Athena Diagnostics Inc

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Gene type:
ClinVar version:
Total variants: 49
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HGVS dbSNP gnomAD frequency
NM_004977.3(KCNC3):c.188A>G (p.Asp63Gly) rs375912738 0.98789
NM_004977.3(KCNC3):c.1929C>T (p.Gly643=) rs111744086 0.01476
NM_004977.3(KCNC3):c.1563G>A (p.Ala521=) rs116768044 0.00495
NM_004977.3(KCNC3):c.984G>A (p.Pro328=) rs114192110 0.00461
NM_004977.3(KCNC3):c.1771A>G (p.Ser591Gly) rs549394447 0.00331
NM_004977.3(KCNC3):c.1404C>T (p.Tyr468=) rs35578310 0.00287
NM_004977.3(KCNC3):c.2093G>A (p.Arg698His) rs144957827 0.00255
NM_004977.3(KCNC3):c.1215C>T (p.Ala405=) rs116590290 0.00109
NM_004977.3(KCNC3):c.315G>C (p.Thr105=) rs368049323 0.00104
NM_004977.3(KCNC3):c.1978+3G>A rs373297576 0.00091
NM_004977.3(KCNC3):c.1875G>T (p.Arg625Ser) rs537912602 0.00064
NM_004977.3(KCNC3):c.1080C>T (p.Thr360=) rs142937043 0.00026
NM_004977.3(KCNC3):c.579C>G (p.Arg193=) rs138237939 0.00024
NM_004977.3(KCNC3):c.871-4G>T rs112673820 0.00016
NM_004977.3(KCNC3):c.1991A>G (p.Asn664Ser) rs199833067 0.00011
NM_004977.3(KCNC3):c.1706C>T (p.Pro569Leu) rs558106649 0.00007
NM_004977.3(KCNC3):c.1752G>A (p.Pro584=) rs1001882554 0.00006
NM_004977.3(KCNC3):c.1338C>T (p.Asn446=) rs140640214 0.00005
NM_004977.3(KCNC3):c.1032G>A (p.Thr344=) rs571327522 0.00004
NM_004977.3(KCNC3):c.1017C>T (p.Asn339=) rs371799397 0.00003
NM_004977.3(KCNC3):c.1065C>T (p.Cys355=) rs761297836 0.00002
NM_004977.3(KCNC3):c.1224C>T (p.Asp408=) rs370533679 0.00002
NM_004977.3(KCNC3):c.1844C>T (p.Ala615Val) rs1432486680 0.00002
NM_004977.3(KCNC3):c.1260C>T (p.Arg420=) rs115066106 0.00001
NM_004977.3(KCNC3):c.1443C>T (p.Gly481=) rs767049102 0.00001
NM_004977.3(KCNC3):c.2023G>A (p.Glu675Lys) rs758477949 0.00001
NM_004977.3(KCNC3):c.2139T>C (p.Tyr713=) rs772962111 0.00001
NM_004977.3(KCNC3):c.991G>A (p.Gly331Arg) rs1305901422 0.00001
NM_004977.3(KCNC3):c.1041C>G (p.Phe347Leu) rs2037069670
NM_004977.3(KCNC3):c.1098C>A (p.Arg366=) rs1455550384
NM_004977.3(KCNC3):c.1153G>A (p.Asp385Asn)
NM_004977.3(KCNC3):c.1196C>T (p.Ser399Leu) rs1437049667
NM_004977.3(KCNC3):c.1198G>T (p.Gly400Cys)
NM_004977.3(KCNC3):c.1229T>C (p.Leu410Pro) rs1601098675
NM_004977.3(KCNC3):c.1259G>A (p.Arg420His) rs104894699
NM_004977.3(KCNC3):c.1268G>A (p.Arg423His) rs797044872
NM_004977.3(KCNC3):c.1354A>G (p.Ile452Val)
NM_004977.3(KCNC3):c.1474A>G (p.Ile492Val)
NM_004977.3(KCNC3):c.1525A>G (p.Met509Val) rs1555781403
NM_004977.3(KCNC3):c.1609G>A (p.Val537Ile)
NM_004977.3(KCNC3):c.1685A>G (p.His562Arg)
NM_004977.3(KCNC3):c.1737ACCCCCGCC[1] (p.Pro583_Pro585del) rs747618525
NM_004977.3(KCNC3):c.1747C>T (p.Pro583Ser)
NM_004977.3(KCNC3):c.1760C>T (p.Pro587Leu) rs554197864
NM_004977.3(KCNC3):c.1794A>G (p.Pro598=) rs2123533646
NM_004977.3(KCNC3):c.1795C>G (p.Pro599Ala)
NM_004977.3(KCNC3):c.1878G>A (p.Gly626=) rs570469383
NM_004977.3(KCNC3):c.1883C>T (p.Ala628Val)
NM_004977.3(KCNC3):c.2130C>T (p.Leu710=) rs1568570611

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