| 15165557 | CV779289 | single nucleotide variant | NM_005990.4(STK10):c.2652+6G>C | not provided [RCV000970975] | benign | 5 | 172054563 | 172054563 | Human | | name |
| 156088957 | CV2202024 | single nucleotide variant | NM_005990.4(STK10):c.98A>G (p.Asn33Ser) | not specified [RCV004075946] | uncertain significance | 5 | 172187945 | 172187945 | Human | | name |
| 156059385 | CV2391743 | single nucleotide variant | NM_005990.4(STK10):c.76G>A (p.Val26Ile) | not specified [RCV004242280] | uncertain significance | 5 | 172187967 | 172187967 | Human | | name |
| 401747330 | CV2688883 | single nucleotide variant | NM_005990.4(STK10):c.32G>A (p.Arg11His) | not specified [RCV004303891] | uncertain significance | 5 | 172188011 | 172188011 | Human | | name |
| 405740657 | CV3334424 | single nucleotide variant | NM_005990.4(STK10):c.99C>G (p.Asn33Lys) | not specified [RCV004465637] | uncertain significance | 5 | 172187944 | 172187944 | Human | | name |
| 407496224 | CV3485461 | single nucleotide variant | NM_005990.4(STK10):c.89T>G (p.Leu30Arg) | not specified [RCV004668078] | uncertain significance | 5 | 172187954 | 172187954 | Human | | name |
| 407496231 | CV3485463 | single nucleotide variant | NM_005990.4(STK10):c.56A>G (p.Lys19Arg) | not specified [RCV004668080] | uncertain significance | 5 | 172187987 | 172187987 | Human | | name |
| 597747415 | CV3618642 | single nucleotide variant | NM_005990.4(STK10):c.32G>T (p.Arg11Leu) | not specified [RCV004866060] | uncertain significance | 5 | 172188011 | 172188011 | Human | | name |
| 597747430 | CV3618645 | single nucleotide variant | NM_005990.4(STK10):c.79C>T (p.Arg27Cys) | not specified [RCV004866063] | uncertain significance | 5 | 172187964 | 172187964 | Human | | name |
| 15165979 | CV699018 | single nucleotide variant | NM_005990.4(STK10):c.351C>T (p.Ala117=) | not provided [RCV000948723] | benign | 5 | 172127392 | 172127392 | Human | | name |
| 15174571 | CV709826 | single nucleotide variant | NM_005990.4(STK10):c.486C>T (p.Asn162=) | not provided [RCV000972744] | benign | 5 | 172117515 | 172117515 | Human | | name |
| 598207177 | CV3919608 | single nucleotide variant | NM_005990.4(STK10):c.277A>G (p.Ile93Val) | not specified [RCV005291239] | uncertain significance | 5 | 172156668 | 172156668 | Human | | name |
| 598207198 | CV3919613 | single nucleotide variant | NM_005990.4(STK10):c.103G>A (p.Val35Met) | not specified [RCV005291242] | uncertain significance | 5 | 172187940 | 172187940 | Human | | name |
| 598207221 | CV3919618 | single nucleotide variant | NM_005990.4(STK10):c.160A>G (p.Lys54Glu) | not specified [RCV005291246] | uncertain significance | 5 | 172156785 | 172156785 | Human | | name |
| 15198917 | CV765026 | single nucleotide variant | NM_005990.4(STK10):c.2757G>A (p.Pro919=) | not provided [RCV000934951] | likely benign | 5 | 172052938 | 172052938 | Human | | name |
| 15198920 | CV765027 | single nucleotide variant | NM_005990.4(STK10):c.1551C>A (p.Ile517=) | not provided [RCV000934952] | likely benign | 5 | 172093415 | 172093415 | Human | | name |
| 156038041 | CV2278895 | single nucleotide variant | NM_005990.4(STK10):c.887G>A (p.Ser296Asn) | not specified [RCV004145596] | uncertain significance | 5 | 172096544 | 172096544 | Human | | name |
| 156137605 | CV2280599 | single nucleotide variant | NM_005990.4(STK10):c.851G>C (p.Ser284Thr) | not specified [RCV004143078] | uncertain significance | 5 | 172105675 | 172105675 | Human | | name |
| 156357920 | CV2318392 | single nucleotide variant | NM_005990.4(STK10):c.357C>A (p.Asp119Glu) | not specified [RCV004179551] | uncertain significance | 5 | 172127386 | 172127386 | Human | | name |
| 156165608 | CV2330061 | single nucleotide variant | NM_005990.4(STK10):c.759C>G (p.Asp253Glu) | not specified [RCV004185553] | uncertain significance | 5 | 172106649 | 172106649 | Human | | name |
| 156283184 | CV2360552 | single nucleotide variant | NM_005990.4(STK10):c.352G>A (p.Val118Met) | not specified [RCV004211312] | uncertain significance | 5 | 172127391 | 172127391 | Human | | name |
| 156106342 | CV2387072 | single nucleotide variant | NM_005990.4(STK10):c.305A>G (p.His102Arg) | not specified [RCV004226815] | uncertain significance | 5 | 172156640 | 172156640 | Human | | name |
| 329375993 | CV2431692 | single nucleotide variant | NM_005990.4(STK10):c.961G>A (p.Gly321Ser) | not specified [RCV004248860] | uncertain significance | 5 | 172096470 | 172096470 | Human | | name |
| 401770395 | CV2715168 | single nucleotide variant | NM_005990.4(STK10):c.803G>A (p.Arg268His) | not specified [RCV004324523] | uncertain significance | 5 | 172105723 | 172105723 | Human | | name |
| 401782944 | CV2716055 | single nucleotide variant | NM_005990.4(STK10):c.495G>A (p.Met165Ile) | not specified [RCV004323304] | uncertain significance | 5 | 172117506 | 172117506 | Human | | name |
| 401760433 | CV2718839 | single nucleotide variant | NM_005990.4(STK10):c.580G>A (p.Gly194Ser) | not specified [RCV004328581] | uncertain significance | 5 | 172107793 | 172107793 | Human | | name |
| 405740614 | CV3334418 | single nucleotide variant | NM_005990.4(STK10):c.416G>T (p.Arg139Leu) | not specified [RCV004465631] | uncertain significance | 5 | 172117585 | 172117585 | Human | | name |
| 405740620 | CV3334419 | single nucleotide variant | NM_005990.4(STK10):c.587C>T (p.Pro196Leu) | not specified [RCV004465632] | uncertain significance | 5 | 172107786 | 172107786 | Human | | name |
| 405740626 | CV3334420 | single nucleotide variant | NM_005990.4(STK10):c.673A>G (p.Ile225Val) | not specified [RCV004465633] | uncertain significance | 5 | 172106735 | 172106735 | Human | | name |
| 405740635 | CV3334421 | single nucleotide variant | NM_005990.4(STK10):c.875C>A (p.Pro292His) | not specified [RCV004465634] | uncertain significance | 5 | 172096556 | 172096556 | Human | | name |
| 405740642 | CV3334422 | single nucleotide variant | NM_005990.4(STK10):c.964C>T (p.Arg322Trp) | not specified [RCV004465635] | uncertain significance | 5 | 172096467 | 172096467 | Human | | name |
| 405740648 | CV3334423 | single nucleotide variant | NM_005990.4(STK10):c.976G>C (p.Glu326Gln) | not specified [RCV004465636] | uncertain significance | 5 | 172096455 | 172096455 | Human | | name |
| 407530114 | CV3485459 | single nucleotide variant | NM_005990.4(STK10):c.502G>A (p.Glu168Lys) | not specified [RCV004681656] | uncertain significance | 5 | 172117499 | 172117499 | Human | | name |
| 407496220 | CV3485460 | single nucleotide variant | NM_005990.4(STK10):c.857C>T (p.Ala286Val) | not specified [RCV004668077] | uncertain significance | 5 | 172105669 | 172105669 | Human | | name |
| 407496235 | CV3485464 | single nucleotide variant | NM_005990.4(STK10):c.659T>C (p.Ile220Thr) | not specified [RCV004668081] | uncertain significance | 5 | 172106749 | 172106749 | Human | | name |
| 597747440 | CV3618647 | single nucleotide variant | NM_005990.4(STK10):c.668T>C (p.Leu223Pro) | not specified [RCV004866065] | uncertain significance | 5 | 172106740 | 172106740 | Human | | name |
| 597703818 | CV3618648 | single nucleotide variant | NM_005990.4(STK10):c.745A>G (p.Ile249Val) | not specified [RCV004860232] | uncertain significance | 5 | 172106663 | 172106663 | Human | | name |
| 598251395 | CV3919609 | single nucleotide variant | NM_005990.4(STK10):c.730C>T (p.Arg244Trp) | not specified [RCV005277879] | uncertain significance | 5 | 172106678 | 172106678 | Human | | name |
| 598251400 | CV3919611 | single nucleotide variant | NM_005990.4(STK10):c.625A>G (p.Met209Val) | not specified [RCV005277880] | uncertain significance | 5 | 172106783 | 172106783 | Human | | name |
| 598207226 | CV3919619 | single nucleotide variant | NM_005990.4(STK10):c.415C>T (p.Arg139Cys) | not specified [RCV005291247] | uncertain significance | 5 | 172117586 | 172117586 | Human | | name |
| 156068546 | CV2222086 | single nucleotide variant | NM_005990.4(STK10):c.1366G>A (p.Ala456Thr) | not specified [RCV004104852] | uncertain significance | 5 | 172093600 | 172093600 | Human | | name |
| 156117858 | CV2231973 | single nucleotide variant | NM_005990.4(STK10):c.1484G>C (p.Ser495Thr) | not specified [RCV004093037] | uncertain significance | 5 | 172093482 | 172093482 | Human | | name |
| 156251514 | CV2232308 | single nucleotide variant | NM_005990.4(STK10):c.2618G>T (p.Cys873Phe) | not specified [RCV004105083] | uncertain significance | 5 | 172054603 | 172054603 | Human | | name |
| 156070916 | CV2232538 | single nucleotide variant | NM_005990.4(STK10):c.2509C>T (p.Arg837Cys) | not specified [RCV004099136] | uncertain significance | 5 | 172055605 | 172055605 | Human | | name |
| 156076878 | CV2251414 | single nucleotide variant | NM_005990.4(STK10):c.1890C>G (p.Asp630Glu) | not specified [RCV004117396] | uncertain significance | 5 | 172082425 | 172082425 | Human | | name |
| 156020825 | CV2264397 | single nucleotide variant | NM_005990.4(STK10):c.1751G>A (p.Ser584Asn) | not specified [RCV004138298] | uncertain significance | 5 | 172083019 | 172083019 | Human | | name |
| 156052737 | CV2269446 | single nucleotide variant | NM_005990.4(STK10):c.2014C>T (p.Pro672Ser) | not specified [RCV004124563] | uncertain significance | 5 | 172064788 | 172064788 | Human | | name |
| 156280902 | CV2295073 | single nucleotide variant | NM_005990.4(STK10):c.1603G>T (p.Val535Leu) | not specified [RCV004156188] | uncertain significance | 5 | 172090314 | 172090314 | Human | | name |
| 156163783 | CV2305531 | single nucleotide variant | NM_005990.4(STK10):c.1316C>T (p.Pro439Leu) | not specified [RCV004165235] | uncertain significance | 5 | 172093650 | 172093650 | Human | | name |
| 156096652 | CV2310199 | single nucleotide variant | NM_005990.4(STK10):c.2215C>T (p.Arg739Trp) | not specified [RCV004163304] | uncertain significance | 5 | 172057471 | 172057471 | Human | | name |
| 156158972 | CV2314575 | single nucleotide variant | NM_005990.4(STK10):c.1246G>A (p.Val416Met) | not specified [RCV004168661] | uncertain significance | 5 | 172093720 | 172093720 | Human | | name |
| 156063951 | CV2316026 | single nucleotide variant | NM_005990.4(STK10):c.2479A>G (p.Ile827Val) | not specified [RCV004165907] | uncertain significance | 5 | 172055635 | 172055635 | Human | | name |
| 156173500 | CV2326855 | single nucleotide variant | NM_005990.4(STK10):c.2458A>C (p.Met820Leu) | not specified [RCV004176682] | uncertain significance | 5 | 172055656 | 172055656 | Human | | name |
| 156306966 | CV2335325 | single nucleotide variant | NM_005990.4(STK10):c.1075G>A (p.Glu359Lys) | not specified [RCV004186887] | likely benign | 5 | 172093891 | 172093891 | Human | | name |
| 155916085 | CV2336081 | single nucleotide variant | NM_005990.4(STK10):c.2413C>T (p.Arg805Trp) | not specified [RCV004189680] | uncertain significance | 5 | 172055701 | 172055701 | Human | | name |
| 155979750 | CV2340082 | single nucleotide variant | NM_005990.4(STK10):c.2840G>A (p.Cys947Tyr) | not specified [RCV004192326] | uncertain significance | 5 | 172044949 | 172044949 | Human | | name |
| 155925378 | CV2348374 | single nucleotide variant | NM_005990.4(STK10):c.2758C>T (p.Arg920Cys) | not specified [RCV004193569] | uncertain significance | 5 | 172052937 | 172052937 | Human | | name |
| 155982575 | CV2351676 | single nucleotide variant | NM_005990.4(STK10):c.2156G>A (p.Arg719Gln) | not specified [RCV004195385] | uncertain significance | 5 | 172061195 | 172061195 | Human | | name |
| 156339714 | CV2367663 | single nucleotide variant | NM_005990.4(STK10):c.2695C>G (p.Leu899Val) | not specified [RCV004211582] | uncertain significance | 5 | 172053000 | 172053000 | Human | | name |
| 156308386 | CV2369915 | single nucleotide variant | NM_005990.4(STK10):c.2050A>G (p.Met684Val) | not specified [RCV004208383] | uncertain significance | 5 | 172064752 | 172064752 | Human | | name |
| 156016894 | CV2370004 | single nucleotide variant | NM_005990.4(STK10):c.1879A>T (p.Met627Leu) | not specified [RCV004210903] | uncertain significance | 5 | 172082436 | 172082436 | Human | | name |
| 155932863 | CV2372179 | single nucleotide variant | NM_005990.4(STK10):c.1595A>G (p.Lys532Arg) | not specified [RCV004216961] | uncertain significance | 5 | 172090322 | 172090322 | Human | | name |
| 155931486 | CV2399852 | single nucleotide variant | NM_005990.4(STK10):c.1787A>T (p.Lys596Ile) | not specified [RCV004246797] | uncertain significance | 5 | 172082983 | 172082983 | Human | | name |
| 329397410 | CV2456134 | single nucleotide variant | NM_005990.4(STK10):c.2086C>T (p.Arg696Trp) | not specified [RCV004273329] | uncertain significance | 5 | 172061265 | 172061265 | Human | | name |
| 401741970 | CV2677479 | single nucleotide variant | NM_005990.4(STK10):c.1261A>G (p.Arg421Gly) | not specified [RCV004289548] | uncertain significance | 5 | 172093705 | 172093705 | Human | | name |
| 401747687 | CV2688984 | single nucleotide variant | NM_005990.4(STK10):c.1081T>A (p.Ser361Thr) | not specified [RCV004305767] | uncertain significance | 5 | 172093885 | 172093885 | Human | | name |
| 401761310 | CV2706296 | single nucleotide variant | NM_005990.4(STK10):c.2210G>A (p.Arg737Gln) | not specified [RCV004314957] | uncertain significance | 5 | 172061141 | 172061141 | Human | | name |
| 401762918 | CV2720128 | single nucleotide variant | NM_005990.4(STK10):c.1259C>G (p.Ala420Gly) | not specified [RCV004323690] | uncertain significance | 5 | 172093707 | 172093707 | Human | | name |
| 401872155 | CV2779561 | single nucleotide variant | NM_005990.4(STK10):c.2435G>A (p.Ser812Asn) | not specified [RCV004351280] | uncertain significance | 5 | 172055679 | 172055679 | Human | | name |
| 405740543 | CV3334407 | single nucleotide variant | NM_005990.4(STK10):c.1007C>T (p.Thr336Ile) | not specified [RCV004465620] | uncertain significance | 5 | 172093959 | 172093959 | Human | | name |
| 405740547 | CV3334408 | single nucleotide variant | NM_005990.4(STK10):c.1094C>G (p.Pro365Arg) | not specified [RCV004465621] | uncertain significance | 5 | 172093872 | 172093872 | Human | | name |
| 405740553 | CV3334409 | single nucleotide variant | NM_005990.4(STK10):c.1978A>G (p.Met660Val) | not specified [RCV004465622] | uncertain significance | 5 | 172082337 | 172082337 | Human | | name |
| 405740563 | CV3334410 | single nucleotide variant | NM_005990.4(STK10):c.1999G>A (p.Glu667Lys) | not specified [RCV004465623] | uncertain significance | 5 | 172064803 | 172064803 | Human | | name |
| 405740569 | CV3334411 | single nucleotide variant | NM_005990.4(STK10):c.2069A>G (p.Lys690Arg) | not specified [RCV004465624] | uncertain significance | 5 | 172064733 | 172064733 | Human | | name |
| 405740577 | CV3334412 | single nucleotide variant | NM_005990.4(STK10):c.2210G>T (p.Arg737Leu) | not specified [RCV004465625] | uncertain significance | 5 | 172061141 | 172061141 | Human | | name |
| 405740579 | CV3334413 | single nucleotide variant | NM_005990.4(STK10):c.2249A>C (p.Gln750Pro) | not specified [RCV004465626] | uncertain significance | 5 | 172057437 | 172057437 | Human | | name |
| 405740592 | CV3334415 | single nucleotide variant | NM_005990.4(STK10):c.2563C>T (p.Arg855Trp) | not specified [RCV004465628] | uncertain significance | 5 | 172054658 | 172054658 | Human | | name |
| 405740609 | CV3334417 | single nucleotide variant | NM_005990.4(STK10):c.2845A>G (p.Asn949Asp) | not specified [RCV004465630] | uncertain significance | 5 | 172044944 | 172044944 | Human | | name |
| 407496210 | CV3485456 | single nucleotide variant | NM_005990.4(STK10):c.2447C>T (p.Thr816Met) | not specified [RCV004668074] | uncertain significance | 5 | 172055667 | 172055667 | Human | | name |
| 407496213 | CV3485457 | single nucleotide variant | NM_005990.4(STK10):c.2600G>A (p.Arg867Gln) | not specified [RCV004668075] | uncertain significance | 5 | 172054621 | 172054621 | Human | | name |
| 407496216 | CV3485458 | single nucleotide variant | NM_005990.4(STK10):c.2797C>T (p.Arg933Trp) | not specified [RCV004668076] | uncertain significance | 5 | 172044992 | 172044992 | Human | | name |
| 407496228 | CV3485462 | single nucleotide variant | NM_005990.4(STK10):c.2816T>C (p.Phe939Ser) | not specified [RCV004668079] | uncertain significance | 5 | 172044973 | 172044973 | Human | | name |
| 407572689 | CV3497171 | single nucleotide variant | NM_005990.4(STK10):c.1450G>T (p.Asp484Tyr) | not provided [RCV004698991] | uncertain significance | 5 | 172093516 | 172093516 | Human | | name |
| 597747420 | CV3618643 | single nucleotide variant | NM_005990.4(STK10):c.1904G>A (p.Arg635His) | not specified [RCV004866061] | uncertain significance | 5 | 172082411 | 172082411 | Human | | name |
| 597747425 | CV3618644 | single nucleotide variant | NM_005990.4(STK10):c.1895C>T (p.Ala632Val) | not specified [RCV004866062] | uncertain significance | 5 | 172082420 | 172082420 | Human | | name |
| 597747435 | CV3618646 | single nucleotide variant | NM_005990.4(STK10):c.2302C>G (p.Leu768Val) | not specified [RCV004866064] | uncertain significance | 5 | 172057384 | 172057384 | Human | | name |
| 598207184 | CV3919610 | single nucleotide variant | NM_005990.4(STK10):c.1897G>A (p.Val633Met) | not specified [RCV005291240] | uncertain significance | 5 | 172082418 | 172082418 | Human | | name |
| 598207191 | CV3919612 | single nucleotide variant | NM_005990.4(STK10):c.1504C>T (p.Leu502Phe) | not specified [RCV005291241] | uncertain significance | 5 | 172093462 | 172093462 | Human | | name |
| 598207203 | CV3919614 | single nucleotide variant | NM_005990.4(STK10):c.1731T>A (p.His577Gln) | not specified [RCV005291243] | uncertain significance | 5 | 172083039 | 172083039 | Human | | name |
| 598251406 | CV3919615 | single nucleotide variant | NM_005990.4(STK10):c.1279G>A (p.Glu427Lys) | not specified [RCV005277881] | uncertain significance | 5 | 172093687 | 172093687 | Human | | name |
| 598207209 | CV3919616 | single nucleotide variant | NM_005990.4(STK10):c.1585C>T (p.Arg529Trp) | not specified [RCV005291244] | uncertain significance | 5 | 172090332 | 172090332 | Human | | name |
| 598207215 | CV3919617 | single nucleotide variant | NM_005990.4(STK10):c.1760A>G (p.His587Arg) | not specified [RCV005291245] | uncertain significance | 5 | 172083010 | 172083010 | Human | | name |
| 15175899 | CV699017 | single nucleotide variant | NM_005990.4(STK10):c.1180C>G (p.Pro394Ala) | not provided [RCV000950697] | benign | 5 | 172093786 | 172093786 | Human | | name |
| 15134885 | CV709825 | single nucleotide variant | NM_005990.4(STK10):c.1559C>T (p.Pro520Leu) | not provided [RCV000965197] | benign | 5 | 172090358 | 172090358 | Human | | name |
