| 401729694 | CV2690445 | single nucleotide variant | NM_032294.3(CAMKK1):c.13C>A (p.Pro5Thr) | not specified [RCV004304217] | uncertain significance | 17 | 3885675 | 3885675 | Human | | name |
| 156273161 | CV2320161 | single nucleotide variant | NM_032294.3(CAMKK1):c.70G>A (p.Asp24Asn) | not specified [RCV004169786] | uncertain significance | 17 | 3885618 | 3885618 | Human | | name |
| 405767223 | CV3302641 | single nucleotide variant | NM_032294.3(CAMKK1):c.38G>A (p.Arg13Gln) | not specified [RCV004434655] | uncertain significance | 17 | 3885650 | 3885650 | Human | | name |
| 598204015 | CV3942973 | single nucleotide variant | NM_032294.3(CAMKK1):c.32A>G (p.Asp11Gly) | not specified [RCV005314719] | uncertain significance | 17 | 3885656 | 3885656 | Human | | name |
| 156247433 | CV2276867 | single nucleotide variant | NM_032294.3(CAMKK1):c.170G>C (p.Ser57Thr) | not specified [RCV004140210] | uncertain significance | 17 | 3885518 | 3885518 | Human | | name |
| 329361859 | CV2468385 | single nucleotide variant | NM_032294.3(CAMKK1):c.140G>A (p.Arg47Gln) | not specified [RCV004275918] | uncertain significance | 17 | 3885548 | 3885548 | Human | | name |
| 401775564 | CV2710617 | single nucleotide variant | NM_032294.3(CAMKK1):c.137C>G (p.Pro46Arg) | not specified [RCV004319533] | uncertain significance | 17 | 3885551 | 3885551 | Human | | name |
| 401935628 | CV2814720 | single nucleotide variant | NM_032294.3(CAMKK1):c.1182C>T (p.Pro394=) | not provided [RCV003413085] | likely benign | 17 | 3869831 | 3869831 | Human | | name |
| 407474535 | CV3424480 | single nucleotide variant | NM_032294.3(CAMKK1):c.289A>G (p.Ser97Gly) | not specified [RCV004600642] | uncertain significance | 17 | 3885399 | 3885399 | Human | | name |
| 407474540 | CV3424481 | single nucleotide variant | NM_032294.3(CAMKK1):c.130C>G (p.Pro44Ala) | not specified [RCV004600643] | uncertain significance | 17 | 3885558 | 3885558 | Human | | name |
| 597763967 | CV3647435 | single nucleotide variant | NM_032294.3(CAMKK1):c.134C>G (p.Pro45Arg) | not specified [RCV004895504] | uncertain significance | 17 | 3885554 | 3885554 | Human | | name |
| 597750773 | CV3647444 | single nucleotide variant | NM_032294.3(CAMKK1):c.194G>A (p.Arg65Gln) | not specified [RCV004892629] | uncertain significance | 17 | 3885494 | 3885494 | Human | | name |
| 156375118 | CV2213501 | single nucleotide variant | NM_032294.3(CAMKK1):c.814G>A (p.Val272Ile) | not specified [RCV004087467] | likely benign | 17 | 3876405 | 3876405 | Human | | name |
| 156025262 | CV2242218 | single nucleotide variant | NM_032294.3(CAMKK1):c.367G>A (p.Val123Met) | not specified [RCV004111250] | uncertain significance | 17 | 3884421 | 3884421 | Human | | name |
| 155978437 | CV2266517 | single nucleotide variant | NM_032294.3(CAMKK1):c.943G>A (p.Ala315Thr) | not specified [RCV004131078] | uncertain significance | 17 | 3876276 | 3876276 | Human | | name |
| 156277521 | CV2352059 | single nucleotide variant | NM_032294.3(CAMKK1):c.864C>A (p.His288Gln) | not specified [RCV004191154] | uncertain significance | 17 | 3876355 | 3876355 | Human | | name |
| 155968818 | CV2391503 | single nucleotide variant | NM_032294.3(CAMKK1):c.298T>A (p.Ser100Thr) | not specified [RCV004239889] | uncertain significance | 17 | 3885390 | 3885390 | Human | | name |
| 401863843 | CV2773480 | single nucleotide variant | NM_032294.3(CAMKK1):c.727T>C (p.Cys243Arg) | not specified [RCV004354113] | uncertain significance | 17 | 3880415 | 3880415 | Human | | name |
| 405767229 | CV3302642 | single nucleotide variant | NM_032294.3(CAMKK1):c.440A>G (p.Asn147Ser) | not specified [RCV004434656] | uncertain significance | 17 | 3883906 | 3883906 | Human | | name |
| 405767235 | CV3302643 | single nucleotide variant | NM_032294.3(CAMKK1):c.457C>T (p.His153Tyr) | not specified [RCV004434657] | uncertain significance | 17 | 3883889 | 3883889 | Human | | name |
| 405767241 | CV3302644 | single nucleotide variant | NM_032294.3(CAMKK1):c.584G>A (p.Arg195Gln) | not specified [RCV004434658] | uncertain significance | 17 | 3883106 | 3883106 | Human | | name |
| 405767249 | CV3302645 | single nucleotide variant | NM_032294.3(CAMKK1):c.719A>G (p.Glu240Gly) | not specified [RCV004434659] | uncertain significance | 17 | 3880423 | 3880423 | Human | | name |
| 405767254 | CV3302646 | single nucleotide variant | NM_032294.3(CAMKK1):c.929C>T (p.Thr310Met) | not specified [RCV004434660] | uncertain significance | 17 | 3876290 | 3876290 | Human | | name |
| 407474520 | CV3424477 | single nucleotide variant | NM_032294.3(CAMKK1):c.758G>A (p.Arg253His) | not specified [RCV004600639] | uncertain significance | 17 | 3880384 | 3880384 | Human | | name |
| 407474527 | CV3424478 | single nucleotide variant | NM_032294.3(CAMKK1):c.757C>T (p.Arg253Cys) | not specified [RCV004600640] | uncertain significance | 17 | 3880385 | 3880385 | Human | | name |
| 597763963 | CV3647433 | single nucleotide variant | NM_032294.3(CAMKK1):c.719A>C (p.Glu240Ala) | not specified [RCV004895503] | uncertain significance | 17 | 3880423 | 3880423 | Human | | name |
| 597763975 | CV3647437 | single nucleotide variant | NM_032294.3(CAMKK1):c.418G>A (p.Gly140Ser) | not specified [RCV004895506] | uncertain significance | 17 | 3883928 | 3883928 | Human | | name |
| 597763983 | CV3647440 | single nucleotide variant | NM_032294.3(CAMKK1):c.363C>G (p.Asp121Glu) | not specified [RCV004895508] | uncertain significance | 17 | 3884425 | 3884425 | Human | | name |
| 597763987 | CV3647441 | single nucleotide variant | NM_032294.3(CAMKK1):c.727T>A (p.Cys243Ser) | not specified [RCV004895509] | uncertain significance | 17 | 3880415 | 3880415 | Human | | name |
| 597763991 | CV3647442 | single nucleotide variant | NM_032294.3(CAMKK1):c.559G>C (p.Ala187Pro) | not specified [RCV004895510] | uncertain significance | 17 | 3883131 | 3883131 | Human | | name |
| 597763995 | CV3647443 | single nucleotide variant | NM_032294.3(CAMKK1):c.992G>C (p.Gly331Ala) | not specified [RCV004895511] | uncertain significance | 17 | 3876227 | 3876227 | Human | | name |
| 156069332 | CV2237122 | single nucleotide variant | NM_032294.3(CAMKK1):c.1066G>A (p.Asp356Asn) | not specified [RCV004114875] | uncertain significance | 17 | 3872612 | 3872612 | Human | | name |
| 156048531 | CV2391014 | single nucleotide variant | NM_032294.3(CAMKK1):c.1305G>T (p.Lys435Asn) | not specified [RCV004235014] | uncertain significance | 17 | 3869523 | 3869523 | Human | | name |
| 156049271 | CV2391075 | single nucleotide variant | NM_032294.3(CAMKK1):c.1276G>A (p.Val426Met) | not specified [RCV004235066] | uncertain significance | 17 | 3869552 | 3869552 | Human | | name |
| 329373720 | CV2434564 | single nucleotide variant | NM_032294.3(CAMKK1):c.1266G>C (p.Glu422Asp) | not specified [RCV004254264] | uncertain significance | 17 | 3869562 | 3869562 | Human | | name |
| 329396373 | CV2462562 | single nucleotide variant | NM_032294.3(CAMKK1):c.1183G>C (p.Glu395Gln) | not specified [RCV004278513] | uncertain significance | 17 | 3869830 | 3869830 | Human | | name |
| 401733818 | CV2687842 | single nucleotide variant | NM_032294.3(CAMKK1):c.1400C>A (p.Ala467Glu) | not specified [RCV004303150] | uncertain significance | 17 | 3865953 | 3865953 | Human | | name |
| 401877263 | CV2764565 | single nucleotide variant | NM_032294.3(CAMKK1):c.1403G>A (p.Arg468Gln) | not specified [RCV004339120] | uncertain significance | 17 | 3865950 | 3865950 | Human | | name |
| 401885584 | CV2778155 | single nucleotide variant | NM_032294.3(CAMKK1):c.1240G>A (p.Glu414Lys) | not specified [RCV004349883] | uncertain significance | 17 | 3869588 | 3869588 | Human | | name |
| 405767203 | CV3302637 | single nucleotide variant | NM_032294.3(CAMKK1):c.1021G>A (p.Val341Ile) | not specified [RCV004434651] | uncertain significance | 17 | 3873438 | 3873438 | Human | | name |
| 405767206 | CV3302638 | single nucleotide variant | NM_032294.3(CAMKK1):c.1141G>A (p.Glu381Lys) | not specified [RCV004434652] | uncertain significance | 17 | 3869872 | 3869872 | Human | | name |
| 405767212 | CV3302639 | single nucleotide variant | NM_032294.3(CAMKK1):c.1186A>G (p.Thr396Ala) | not specified [RCV004434653] | uncertain significance | 17 | 3869827 | 3869827 | Human | | name |
| 405767218 | CV3302640 | single nucleotide variant | NM_032294.3(CAMKK1):c.1370G>A (p.Arg457His) | not specified [RCV004434654] | uncertain significance | 17 | 3865983 | 3865983 | Human | | name |
| 407474516 | CV3424476 | single nucleotide variant | NM_032294.3(CAMKK1):c.1456T>C (p.Phe486Leu) | not specified [RCV004600638] | uncertain significance | 17 | 3862273 | 3862273 | Human | | name |
| 407474531 | CV3424479 | single nucleotide variant | NM_032294.3(CAMKK1):c.1136G>T (p.Ser379Ile) | not specified [RCV004600641] | uncertain significance | 17 | 3869877 | 3869877 | Human | | name |
| 597763959 | CV3647432 | single nucleotide variant | NM_032294.3(CAMKK1):c.1040T>C (p.Val347Ala) | not specified [RCV004895502] | uncertain significance | 17 | 3873419 | 3873419 | Human | | name |
| 597763971 | CV3647436 | single nucleotide variant | NM_032294.3(CAMKK1):c.1237G>A (p.Gly413Arg) | not specified [RCV004895505] | uncertain significance | 17 | 3869591 | 3869591 | Human | | name |
| 597763979 | CV3647438 | single nucleotide variant | NM_032294.3(CAMKK1):c.1447A>C (p.Lys483Gln) | not specified [RCV004895507] | uncertain significance | 17 | 3862282 | 3862282 | Human | | name |
| 597750768 | CV3647439 | single nucleotide variant | NM_032294.3(CAMKK1):c.1459G>C (p.Gly487Arg) | not specified [RCV004892628] | uncertain significance | 17 | 3862270 | 3862270 | Human | | name |
| 598212640 | CV3942975 | single nucleotide variant | NM_032294.3(CAMKK1):c.1332G>C (p.Trp444Cys) | not specified [RCV005316195] | uncertain significance | 17 | 3869496 | 3869496 | Human | | name |
| 598204029 | CV3942976 | single nucleotide variant | NM_032294.3(CAMKK1):c.1454G>A (p.Gly485Glu) | not specified [RCV005314721] | uncertain significance | 17 | 3862275 | 3862275 | Human | | name |
| 8636162 | CV91386 | single nucleotide variant | NM_032294.2(CAMKK1):c.1252C>T (p.Pro418Ser) | Malignant melanoma [RCV000071484] | not provided | 17 | 3869576 | 3869576 | Human | | name |