ClinVar Miner

List of variants in gene KCNB1 reported as likely benign by GeneDx

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Gene type:
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Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_004975.4(KCNB1):c.567+49C>T rs35235111 0.03268
NM_004975.4(KCNB1):c.-51G>C rs536669582 0.00686
NC_000020.11:g.49482899G>A rs58482942 0.00522
NM_004975.4(KCNB1):c.51G>A (p.Pro17=) rs772184358 0.00022
NM_004975.4(KCNB1):c.-13G>A rs1010817242 0.00019
NM_004975.4(KCNB1):c.2520C>T (p.Asp840=) rs372147544 0.00017
NM_004975.4(KCNB1):c.1551G>A (p.Ser517=) rs377030406 0.00014
NM_004975.4(KCNB1):c.*17G>A rs368159173 0.00012
NM_004975.4(KCNB1):c.1367G>A (p.Arg456Gln) rs761082551 0.00012
NM_004975.4(KCNB1):c.2364G>A (p.Thr788=) rs112132596 0.00012
NM_004975.4(KCNB1):c.630G>A (p.Thr210=) rs150723418 0.00011
NM_004975.4(KCNB1):c.1997C>T (p.Pro666Leu) rs201212125 0.00010
NM_004975.4(KCNB1):c.1305T>C (p.Ala435=) rs201403239 0.00009
NM_004975.4(KCNB1):c.1654G>A (p.Ala552Thr) rs146429493 0.00009
NM_004975.4(KCNB1):c.1861G>T (p.Ala621Ser) rs201960228 0.00009
NM_004975.4(KCNB1):c.2115C>T (p.Val705=) rs199910304 0.00009
NM_004975.4(KCNB1):c.2472C>T (p.Gly824=) rs375177375 0.00009
NM_004975.4(KCNB1):c.-47G>A rs569121895 0.00006
NM_004975.4(KCNB1):c.1655C>T (p.Ala552Val) rs370974891 0.00006
NM_004975.4(KCNB1):c.1905T>C (p.Gly635=) rs117166054 0.00006
NM_004975.4(KCNB1):c.2375C>T (p.Ser792Leu) rs777053418 0.00006
NM_004975.4(KCNB1):c.546C>T (p.Pro182=) rs373223027 0.00006
NM_004975.4(KCNB1):c.1705G>A (p.Val569Ile) rs376490656 0.00005
NM_004975.4(KCNB1):c.2249C>T (p.Ala750Val) rs750157634 0.00005
NM_004975.4(KCNB1):c.2250G>A (p.Ala750=) rs368736609 0.00005
NM_004975.4(KCNB1):c.2327A>G (p.Lys776Arg) rs756982426 0.00005
NM_004975.4(KCNB1):c.39C>T (p.Thr13=) rs775536644 0.00005
NM_004975.4(KCNB1):c.504C>T (p.Cys168=) rs139960830 0.00005
NM_004975.4(KCNB1):c.855C>T (p.Ser285=) rs367938880 0.00005
NM_004975.4(KCNB1):c.2093G>A (p.Arg698Gln) rs1449919002 0.00004
NM_004975.4(KCNB1):c.2376G>A (p.Ser792=) rs750105922 0.00004
NM_004975.4(KCNB1):c.568-5C>T rs185995580 0.00004
NM_004975.4(KCNB1):c.114G>T (p.Gly38=) rs1233894851 0.00003
NM_004975.4(KCNB1):c.598G>A (p.Val200Ile) rs748573940 0.00003
NM_004975.4(KCNB1):c.1788A>T (p.Thr596=) rs373119881 0.00002
NM_004975.4(KCNB1):c.2009G>A (p.Arg670Gln) rs753575587 0.00002
NM_004975.4(KCNB1):c.2058C>T (p.Pro686=) rs908785527 0.00002
NM_004975.4(KCNB1):c.2207G>A (p.Arg736Gln) rs151175979 0.00002
NM_004975.4(KCNB1):c.2516C>T (p.Pro839Leu) rs761070687 0.00002
NM_004975.4(KCNB1):c.568-20C>T rs934317402 0.00002
NM_004975.4(KCNB1):c.568-9T>C rs771401083 0.00002
NM_004975.4(KCNB1):c.693C>T (p.His231=) rs765195036 0.00002
NM_004975.4(KCNB1):c.96G>A (p.Arg32=) rs781213174 0.00002
NM_004975.4(KCNB1):c.-29C>G rs1044884348 0.00001
NM_004975.4(KCNB1):c.1116C>G (p.Thr372=) rs1347667767 0.00001
NM_004975.4(KCNB1):c.1693A>G (p.Ile565Val) rs761452916 0.00001
NM_004975.4(KCNB1):c.2055C>A (p.Leu685=) rs200849612 0.00001
NM_004975.4(KCNB1):c.2178C>T (p.Tyr726=) rs1027150424 0.00001
NM_004975.4(KCNB1):c.411C>T (p.Tyr137=) rs747090668 0.00001
NM_004975.4(KCNB1):c.711C>T (p.Ile237=) rs1020438851 0.00001
NM_004975.4(KCNB1):c.81G>A (p.Lys27=) rs910155179 0.00001
NM_004975.4(KCNB1):c.900C>A (p.Arg300=) rs1057523982 0.00001
NM_004975.4(KCNB1):c.*71A>C rs147708122
NM_004975.4(KCNB1):c.1326T>C (p.Asn442=) rs1601070955
NM_004975.4(KCNB1):c.1503T>C (p.Ser501=) rs1601070677
NM_004975.4(KCNB1):c.1800G>A (p.Glu600=) rs1290919811
NM_004975.4(KCNB1):c.1821C>T (p.Ser607=) rs1057522569
NM_004975.4(KCNB1):c.2324C>G (p.Pro775Arg) rs530927636
NM_004975.4(KCNB1):c.243C>T (p.Asn81=) rs1295557969
NM_004975.4(KCNB1):c.813G>A (p.Leu271=) rs763166574
NM_004975.4(KCNB1):c.939C>T (p.His313=) rs1304387636

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