| 156336601 | CV2228568 | single nucleotide variant | NM_001039574.3(KCNC4):c.1820-649G>C | not specified [RCV004092803] | uncertain significance | 1 | 110232262 | 110232262 | Human | | name |
| 405806545 | CV3268506 | single nucleotide variant | NM_001039574.3(KCNC4):c.1820-652C>T | not specified [RCV004406020] | uncertain significance | 1 | 110232259 | 110232259 | Human | | name |
| 407467918 | CV3444953 | single nucleotide variant | NM_001039574.3(KCNC4):c.1820-683C>A | not specified [RCV004636062] | uncertain significance | 1 | 110232228 | 110232228 | Human | | name |
| 597787567 | CV3687278 | single nucleotide variant | NM_001039574.3(KCNC4):c.1820-675G>A | not specified [RCV004932531] | uncertain significance | 1 | 110232236 | 110232236 | Human | | name |
| 598259468 | CV3980184 | single nucleotide variant | NM_001039574.3(KCNC4):c.1820-676C>A | not specified [RCV005347427] | uncertain significance | 1 | 110232235 | 110232235 | Human | | name |
| 8628788 | CV83932 | single nucleotide variant | NM_001039574.2(KCNC4):c.1819+131C>T | Malignant melanoma [RCV000064013] | not provided | 1 | 110226309 | 110226309 | Human | | name |
| 405697036 | CV3226802 | single nucleotide variant | NM_001039574.3(KCNC4):c.567G>C (p.Leu189=) | not provided [RCV003993196] | likely benign | 1 | 110212066 | 110212066 | Human | | name |
| 15197143 | CV745561 | single nucleotide variant | NM_001039574.3(KCNC4):c.786C>T (p.Arg262=) | not provided [RCV000911895] | likely benign | 1 | 110223071 | 110223071 | Human | | name |
| 401767838 | CV2729954 | single nucleotide variant | NM_001039574.3(KCNC4):c.226A>T (p.Thr76Ser) | not specified [RCV004332948] | likely benign | 1 | 110211725 | 110211725 | Human | | name |
| 401767839 | CV2729955 | single nucleotide variant | NM_001039574.3(KCNC4):c.242T>C (p.Val81Ala) | not specified [RCV004332949] | likely benign | 1 | 110211741 | 110211741 | Human | | name |
| 405695053 | CV3226557 | single nucleotide variant | NM_001039574.3(KCNC4):c.1734C>A (p.Thr578=) | not provided [RCV003992950] | likely benign | 1 | 110226093 | 110226093 | Human | | name |
| 405806324 | CV3268497 | single nucleotide variant | NM_001039574.3(KCNC4):c.134C>T (p.Thr45Met) | not specified [RCV004406011] | uncertain significance | 1 | 110211633 | 110211633 | Human | | name |
| 405806342 | CV3268507 | single nucleotide variant | NM_001039574.3(KCNC4):c.205G>T (p.Asp69Tyr) | not specified [RCV004406021] | uncertain significance | 1 | 110211704 | 110211704 | Human | | name |
| 597787563 | CV3687277 | single nucleotide variant | NM_001039574.3(KCNC4):c.106G>A (p.Glu36Lys) | not specified [RCV004932530] | uncertain significance | 1 | 110211605 | 110211605 | Human | | name |
| 155996672 | CV2250478 | single nucleotide variant | NM_001039574.3(KCNC4):c.605C>T (p.Ser202Phe) | not specified [RCV004127344] | uncertain significance | 1 | 110212104 | 110212104 | Human | | name |
| 156068895 | CV2270945 | single nucleotide variant | NM_001039574.3(KCNC4):c.586G>C (p.Ala196Pro) | not specified [RCV004131980] | uncertain significance | 1 | 110212085 | 110212085 | Human | | name |
| 156241461 | CV2286120 | single nucleotide variant | NM_001039574.3(KCNC4):c.302G>A (p.Gly101Asp) | not specified [RCV004145792] | uncertain significance | 1 | 110211801 | 110211801 | Human | | name |
| 156172896 | CV2326810 | single nucleotide variant | NM_001039574.3(KCNC4):c.760G>A (p.Asp254Asn) | not specified [RCV004176645] | uncertain significance | 1 | 110223045 | 110223045 | Human | | name |
| 156129019 | CV2358567 | single nucleotide variant | NM_001039574.3(KCNC4):c.520A>G (p.Ser174Gly) | not specified [RCV004207449] | likely benign | 1 | 110212019 | 110212019 | Human | | name |
| 156004325 | CV2400974 | single nucleotide variant | NM_001039574.3(KCNC4):c.767A>G (p.Asn256Ser) | not specified [RCV004244259] | uncertain significance | 1 | 110223052 | 110223052 | Human | | name |
| 329361504 | CV2437584 | single nucleotide variant | NM_001039574.3(KCNC4):c.577G>C (p.Glu193Gln) | not specified [RCV004258864] | uncertain significance | 1 | 110212076 | 110212076 | Human | | name |
| 329361366 | CV2459414 | single nucleotide variant | NM_001039574.3(KCNC4):c.599C>T (p.Ala200Val) | not specified [RCV004275106] | uncertain significance | 1 | 110212098 | 110212098 | Human | | name |
| 401726019 | CV2699030 | single nucleotide variant | NM_001039574.3(KCNC4):c.805G>A (p.Val269Met) | not specified [RCV004303552] | uncertain significance | 1 | 110223090 | 110223090 | Human | | name |
| 401750868 | CV2700097 | single nucleotide variant | NM_001039574.3(KCNC4):c.505A>G (p.Ser169Gly) | not specified [RCV004310508] | likely benign | 1 | 110212004 | 110212004 | Human | | name |
| 401750871 | CV2700098 | single nucleotide variant | NM_001039574.3(KCNC4):c.507C>G (p.Ser169Arg) | not specified [RCV004310509] | uncertain significance | 1 | 110212006 | 110212006 | Human | | name |
| 401750873 | CV2700099 | single nucleotide variant | NM_001039574.3(KCNC4):c.509G>C (p.Gly170Ala) | not specified [RCV004310510] | uncertain significance | 1 | 110212008 | 110212008 | Human | | name |
| 401885615 | CV2774977 | single nucleotide variant | NM_001039574.3(KCNC4):c.529G>A (p.Ala177Thr) | not specified [RCV004346375] | uncertain significance | 1 | 110212028 | 110212028 | Human | | name |
| 405806345 | CV3268509 | single nucleotide variant | NM_001039574.3(KCNC4):c.496G>C (p.Gly166Arg) | not specified [RCV004406023] | uncertain significance | 1 | 110211995 | 110211995 | Human | | name |
| 405806349 | CV3268511 | single nucleotide variant | NM_001039574.3(KCNC4):c.796A>G (p.Ile266Val) | not specified [RCV004406025] | uncertain significance | 1 | 110223081 | 110223081 | Human | | name |
| 407467911 | CV3444949 | single nucleotide variant | NM_001039574.3(KCNC4):c.547G>A (p.Glu183Lys) | not specified [RCV004636058] | uncertain significance | 1 | 110212046 | 110212046 | Human | | name |
| 407467914 | CV3444951 | single nucleotide variant | NM_001039574.3(KCNC4):c.643C>T (p.Leu215Phe) | not specified [RCV004636060] | uncertain significance | 1 | 110212142 | 110212142 | Human | | name |
| 407467916 | CV3444952 | single nucleotide variant | NM_001039574.3(KCNC4):c.598G>T (p.Ala200Ser) | not specified [RCV004636061] | uncertain significance | 1 | 110212097 | 110212097 | Human | | name |
| 597787570 | CV3687279 | single nucleotide variant | NM_001039574.3(KCNC4):c.764G>A (p.Arg255His) | not specified [RCV004932532] | uncertain significance | 1 | 110223049 | 110223049 | Human | | name |
| 597787575 | CV3687280 | single nucleotide variant | NM_001039574.3(KCNC4):c.785G>T (p.Arg262Leu) | not specified [RCV004932533] | uncertain significance | 1 | 110223070 | 110223070 | Human | | name |
| 597787581 | CV3687282 | single nucleotide variant | NM_001039574.3(KCNC4):c.763C>T (p.Arg255Cys) | not specified [RCV004932535] | uncertain significance | 1 | 110223048 | 110223048 | Human | | name |
| 598259451 | CV3980176 | single nucleotide variant | NM_001039574.3(KCNC4):c.809A>G (p.His270Arg) | not specified [RCV005347424] | likely benign | 1 | 110223094 | 110223094 | Human | | name |
| 598259457 | CV3980177 | single nucleotide variant | NM_001039574.3(KCNC4):c.496G>A (p.Gly166Arg) | not specified [RCV005347425] | uncertain significance | 1 | 110211995 | 110211995 | Human | | name |
| 598234782 | CV3980179 | single nucleotide variant | NM_001039574.3(KCNC4):c.922G>C (p.Asp308His) | not specified [RCV005363559] | uncertain significance | 1 | 110223207 | 110223207 | Human | | name |
| 598234789 | CV3980180 | single nucleotide variant | NM_001039574.3(KCNC4):c.545G>C (p.Arg182Pro) | not specified [RCV005363560] | uncertain significance | 1 | 110212044 | 110212044 | Human | | name |
| 598259461 | CV3980182 | single nucleotide variant | NM_001039574.3(KCNC4):c.616C>G (p.Arg206Gly) | not specified [RCV005347426] | uncertain significance | 1 | 110212115 | 110212115 | Human | | name |
| 598212764 | CV3980185 | single nucleotide variant | NM_001039574.3(KCNC4):c.933G>C (p.Lys311Asn) | not specified [RCV005358874] | uncertain significance | 1 | 110223218 | 110223218 | Human | | name |
| 156382312 | CV2212709 | single nucleotide variant | NM_001039574.3(KCNC4):c.1225C>G (p.Pro409Ala) | not specified [RCV004085214] | uncertain significance | 1 | 110223510 | 110223510 | Human | | name |
| 156123616 | CV2234064 | single nucleotide variant | NM_001039574.3(KCNC4):c.1238G>A (p.Arg413Gln) | not specified [RCV004106170] | uncertain significance | 1 | 110223523 | 110223523 | Human | | name |
| 156072398 | CV2289945 | single nucleotide variant | NM_001039574.3(KCNC4):c.1580C>T (p.Ala527Val) | not specified [RCV004150595] | uncertain significance | 1 | 110223865 | 110223865 | Human | | name |
| 156164885 | CV2315125 | single nucleotide variant | NM_001039574.3(KCNC4):c.1599C>G (p.Ile533Met) | not specified [RCV004165306] | uncertain significance | 1 | 110223884 | 110223884 | Human | | name |
| 155919953 | CV2343262 | single nucleotide variant | NM_001039574.3(KCNC4):c.1447A>G (p.Met483Val) | not specified [RCV004194885] | uncertain significance | 1 | 110223732 | 110223732 | Human | | name |
| 155938906 | CV2376419 | single nucleotide variant | NM_001039574.3(KCNC4):c.1786G>A (p.Asp596Asn) | not specified [RCV004220603] | uncertain significance | 1 | 110226145 | 110226145 | Human | | name |
| 156221777 | CV2394518 | single nucleotide variant | NM_001039574.3(KCNC4):c.1493G>A (p.Arg498Gln) | not specified [RCV004240876] | uncertain significance | 1 | 110223778 | 110223778 | Human | | name |
| 156083405 | CV2394962 | single nucleotide variant | NM_001039574.3(KCNC4):c.1714C>T (p.Arg572Trp) | not specified [RCV004234610] | uncertain significance | 1 | 110226073 | 110226073 | Human | | name |
| 329375553 | CV2431562 | single nucleotide variant | NM_001039574.3(KCNC4):c.1727G>A (p.Arg576His) | not specified [RCV004254714] | uncertain significance | 1 | 110226086 | 110226086 | Human | | name |
| 329367466 | CV2456818 | single nucleotide variant | NM_001039574.3(KCNC4):c.1745G>A (p.Arg582Lys) | not specified [RCV004270787] | uncertain significance | 1 | 110226104 | 110226104 | Human | | name |
| 401721896 | CV2680729 | single nucleotide variant | NM_001039574.3(KCNC4):c.1621A>G (p.Lys541Glu) | not specified [RCV004291338] | uncertain significance | 1 | 110225980 | 110225980 | Human | | name |
| 401721961 | CV2680758 | single nucleotide variant | NM_001039574.3(KCNC4):c.1813C>T (p.Arg605Trp) | not specified [RCV004293411] | uncertain significance | 1 | 110226172 | 110226172 | Human | | name |
| 401776279 | CV2706955 | single nucleotide variant | NM_001039574.3(KCNC4):c.1583G>A (p.Arg528Gln) | not specified [RCV004321558] | uncertain significance | 1 | 110223868 | 110223868 | Human | | name |
| 401781567 | CV2722168 | single nucleotide variant | NM_001039574.3(KCNC4):c.1426G>A (p.Gly476Ser) | not specified [RCV004328739] | uncertain significance | 1 | 110223711 | 110223711 | Human | | name |
| 405806322 | CV3268496 | single nucleotide variant | NM_001039574.3(KCNC4):c.1013C>G (p.Ala338Gly) | not specified [RCV004406010] | uncertain significance | 1 | 110223298 | 110223298 | Human | | name |
| 405806326 | CV3268498 | single nucleotide variant | NM_001039574.3(KCNC4):c.1474C>T (p.Arg492Trp) | not specified [RCV004406012] | uncertain significance | 1 | 110223759 | 110223759 | Human | | name |
| 405806328 | CV3268499 | single nucleotide variant | NM_001039574.3(KCNC4):c.1489C>T (p.Pro497Ser) | not specified [RCV004406013] | uncertain significance | 1 | 110223774 | 110223774 | Human | | name |
| 405806331 | CV3268501 | single nucleotide variant | NM_001039574.3(KCNC4):c.1523G>A (p.Cys508Tyr) | not specified [RCV004406015] | uncertain significance | 1 | 110223808 | 110223808 | Human | | name |
| 405806333 | CV3268502 | single nucleotide variant | NM_001039574.3(KCNC4):c.1612G>A (p.Ala538Thr) | not specified [RCV004406016] | uncertain significance | 1 | 110223897 | 110223897 | Human | | name |
| 405806334 | CV3268503 | single nucleotide variant | NM_001039574.3(KCNC4):c.1705G>A (p.Glu569Lys) | not specified [RCV004406017] | uncertain significance | 1 | 110226064 | 110226064 | Human | | name |
| 405806336 | CV3268504 | single nucleotide variant | NM_001039574.3(KCNC4):c.1721T>C (p.Leu574Pro) | not specified [RCV004406018] | uncertain significance | 1 | 110226080 | 110226080 | Human | | name |
| 405806338 | CV3268505 | single nucleotide variant | NM_001039574.3(KCNC4):c.1798G>A (p.Ala600Thr) | not specified [RCV004406019] | uncertain significance | 1 | 110226157 | 110226157 | Human | | name |
| 407467909 | CV3444948 | single nucleotide variant | NM_001039574.3(KCNC4):c.1724G>A (p.Arg575Gln) | not specified [RCV004636057] | uncertain significance | 1 | 110226083 | 110226083 | Human | | name |
| 407467912 | CV3444950 | single nucleotide variant | NM_001039574.3(KCNC4):c.1514C>T (p.Pro505Leu) | not specified [RCV004636059] | uncertain significance | 1 | 110223799 | 110223799 | Human | | name |
| 597787551 | CV3687274 | single nucleotide variant | NM_001039574.3(KCNC4):c.1726C>T (p.Arg576Cys) | not specified [RCV004932527] | uncertain significance | 1 | 110226085 | 110226085 | Human | | name |
| 597787553 | CV3687275 | single nucleotide variant | NM_001039574.3(KCNC4):c.1700C>T (p.Thr567Ile) | not specified [RCV004932528] | uncertain significance | 1 | 110226059 | 110226059 | Human | | name |
| 597787577 | CV3687281 | single nucleotide variant | NM_001039574.3(KCNC4):c.1717G>A (p.Ala573Thr) | not specified [RCV004932534] | uncertain significance | 1 | 110226076 | 110226076 | Human | | name |
| 598212758 | CV3980181 | single nucleotide variant | NM_001039574.3(KCNC4):c.1573C>T (p.Pro525Ser) | not specified [RCV005358873] | uncertain significance | 1 | 110223858 | 110223858 | Human | | name |
| 598234796 | CV3980183 | single nucleotide variant | NM_001039574.3(KCNC4):c.1690T>G (p.Ser564Ala) | not specified [RCV005363561] | uncertain significance | 1 | 110226049 | 110226049 | Human | | name |
