ClinVar Miner

List of variants in gene KCNC3 reported as benign by Athena Diagnostics Inc

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Gene type:
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Total variants: 20
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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.1752G>A (p.Pro584=) rs1001882554 0.00006
NM_004977.3(KCNC3):c.1017C>T (p.Asn339=) rs371799397 0.00003
NM_004977.3(KCNC3):c.1224C>T (p.Asp408=) rs370533679 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.1760C>T (p.Pro587Leu) rs554197864

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