| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.56882174_56882189del | CA645557020 | MAP3K1 | c.2974_2989del (p.Ser992LeufsTer?) c.2596_2611del (p.Ser866LeufsTer?) c.2719_2734del (p.Ser907LeufsTer?) c.2695_2710del (p.Ser899LeufsTer?) c.2563_2578del (p.Ser855LeufsTer?) c.2485_2500del (p.Ser829LeufsTer?) n.3005_3020del | COSMIC |
| 5 | g.56882184C>A | CA359787406 | MAP3K1 | c.2984C>A (p.Ala995Asp) c.2606C>A (p.Ala869Asp) c.2729C>A (p.Ala910Asp) c.2705C>A (p.Ala902Asp) c.2573C>A (p.Ala858Asp) c.2495C>A (p.Ala832Asp) n.3015C>A | dbSNP |
| 5 | g.56882184C>G | CA359787407 | MAP3K1 | c.2984C>G (p.Ala995Gly) c.2606C>G (p.Ala869Gly) c.2729C>G (p.Ala910Gly) c.2705C>G (p.Ala902Gly) c.2573C>G (p.Ala858Gly) c.2495C>G (p.Ala832Gly) n.3015C>G | |
| 5 | g.56882184C>T | CA359787408 | MAP3K1 | c.2984C>T (p.Ala995Val) c.2606C>T (p.Ala869Val) c.2729C>T (p.Ala910Val) c.2705C>T (p.Ala902Val) c.2573C>T (p.Ala858Val) c.2495C>T (p.Ala832Val) n.3015C>T | dbSNP |
| 5 | g.56882185T>A | CA444399423 | MAP3K1 | c.2985T>A (p.Ala995=) c.2607T>A (p.Ala869=) c.2730T>A (p.Ala910=) c.2706T>A (p.Ala902=) c.2574T>A (p.Ala858=) c.2496T>A (p.Ala832=) n.3016T>A | |
| 5 | g.56882185T>C | CA444399422 | MAP3K1 | c.2985T>C (p.Ala995=) c.2607T>C (p.Ala869=) c.2730T>C (p.Ala910=) c.2706T>C (p.Ala902=) c.2574T>C (p.Ala858=) c.2496T>C (p.Ala832=) n.3016T>C | |
| 5 | g.56882185T>G | CA444399421 | MAP3K1 | c.2985T>G (p.Ala995=) c.2607T>G (p.Ala869=) c.2730T>G (p.Ala910=) c.2706T>G (p.Ala902=) c.2574T>G (p.Ala858=) c.2496T>G (p.Ala832=) n.3016T>G | |
| 5 | g.56882186G>A | CA359787409 | MAP3K1 | c.2986G>A (p.Gly996Ser) c.2608G>A (p.Gly870Ser) c.2731G>A (p.Gly911Ser) c.2707G>A (p.Gly903Ser) c.2575G>A (p.Gly859Ser) c.2497G>A (p.Gly833Ser) n.3017G>A | dbSNP gnomAD v4 |
| 5 | g.56882186G>C | CA359787411 | MAP3K1 | c.2986G>C (p.Gly996Arg) c.2608G>C (p.Gly870Arg) c.2731G>C (p.Gly911Arg) c.2707G>C (p.Gly903Arg) c.2575G>C (p.Gly859Arg) c.2497G>C (p.Gly833Arg) n.3017G>C | dbSNP |
| 5 | g.56882186G>T | CA359787410 | MAP3K1 | c.2986G>T (p.Gly996Cys) c.2608G>T (p.Gly870Cys) c.2731G>T (p.Gly911Cys) c.2707G>T (p.Gly903Cys) c.2575G>T (p.Gly859Cys) c.2497G>T (p.Gly833Cys) n.3017G>T | COSMIC |
| 5 | g.56882187del | CA2708986523 | MAP3K1 | c.2987del (p.Gly996AlafsTer?) c.2609del (p.Gly870AlafsTer?) c.2732del (p.Gly911AlafsTer?) c.2708del (p.Gly903AlafsTer?) c.2576del (p.Gly859AlafsTer?) c.2498del (p.Gly833AlafsTer?) n.3018del | dbSNP |
| 5 | g.56882187G>A | CA359787412 | MAP3K1 | c.2987G>A (p.Gly996Asp) c.2609G>A (p.Gly870Asp) c.2732G>A (p.Gly911Asp) c.2708G>A (p.Gly903Asp) c.2576G>A (p.Gly859Asp) c.2498G>A (p.Gly833Asp) n.3018G>A | dbSNP |
| 5 | g.56882187G>C | CA359787413 | MAP3K1 | c.2987G>C (p.Gly996Ala) c.2609G>C (p.Gly870Ala) c.2732G>C (p.Gly911Ala) c.2708G>C (p.Gly903Ala) c.2576G>C (p.Gly859Ala) c.2498G>C (p.Gly833Ala) n.3018G>C | dbSNP |
| 5 | g.56882187G>T | CA359787414 | MAP3K1 | c.2987G>T (p.Gly996Val) c.2609G>T (p.Gly870Val) c.2732G>T (p.Gly911Val) c.2708G>T (p.Gly903Val) c.2576G>T (p.Gly859Val) c.2498G>T (p.Gly833Val) n.3018G>T | dbSNP |
| 5 | g.56882188C>A | CA444399429 | MAP3K1 | c.2988C>A (p.Gly996=) c.2610C>A (p.Gly870=) c.2733C>A (p.Gly911=) c.2709C>A (p.Gly903=) c.2577C>A (p.Gly859=) c.2499C>A (p.Gly833=) n.3019C>A | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.56882188C= | CA1548139493 | MAP3K1 | c.2988C= (p.Gly996=) c.2610C= (p.Gly870=) c.2733C= (p.Gly911=) c.2709C= (p.Gly903=) c.2577C= (p.Gly859=) c.2499C= (p.Gly833=) n.3019C= | |
| 5 | g.56882188C>G | CA444399427 | MAP3K1 | c.2988C>G (p.Gly996=) c.2610C>G (p.Gly870=) c.2733C>G (p.Gly911=) c.2709C>G (p.Gly903=) c.2577C>G (p.Gly859=) c.2499C>G (p.Gly833=) n.3019C>G | dbSNP |
| 5 | g.56882188C>T | CA444399425 | MAP3K1 | c.2988C>T (p.Gly996=) c.2610C>T (p.Gly870=) c.2733C>T (p.Gly911=) c.2709C>T (p.Gly903=) c.2577C>T (p.Gly859=) c.2499C>T (p.Gly833=) n.3019C>T | dbSNP gnomAD v4 |
| 5 | g.56882189A= | CA1548139494 | MAP3K1 | c.2989A= (p.Thr997=) c.2611A= (p.Thr871=) c.2734A= (p.Thr912=) c.2710A= (p.Thr904=) c.2578A= (p.Thr860=) c.2500A= (p.Thr834=) n.3020A= | |
| 5 | g.56882189A>C | CA359787415 | MAP3K1 | c.2989A>C (p.Thr997Pro) c.2611A>C (p.Thr871Pro) c.2734A>C (p.Thr912Pro) c.2710A>C (p.Thr904Pro) c.2578A>C (p.Thr860Pro) c.2500A>C (p.Thr834Pro) n.3020A>C | |
| 5 | g.56882189A>G | CA359787416 | MAP3K1 | c.2989A>G (p.Thr997Ala) c.2611A>G (p.Thr871Ala) c.2734A>G (p.Thr912Ala) c.2710A>G (p.Thr904Ala) c.2578A>G (p.Thr860Ala) c.2500A>G (p.Thr834Ala) n.3020A>G | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.56882189A>T | CA359787417 | MAP3K1 | c.2989A>T (p.Thr997Ser) c.2611A>T (p.Thr871Ser) c.2734A>T (p.Thr912Ser) c.2710A>T (p.Thr904Ser) c.2578A>T (p.Thr860Ser) c.2500A>T (p.Thr834Ser) n.3020A>T | dbSNP |
| 5 | g.56882190C>A | CA359787418 | MAP3K1 | c.2990C>A (p.Thr997Asn) c.2612C>A (p.Thr871Asn) c.2735C>A (p.Thr912Asn) c.2711C>A (p.Thr904Asn) c.2579C>A (p.Thr860Asn) c.2501C>A (p.Thr834Asn) n.3021C>A | dbSNP |
| 5 | g.56882190C= | CA1548139495 | MAP3K1 | c.2990C= (p.Thr997=) c.2612C= (p.Thr871=) c.2735C= (p.Thr912=) c.2711C= (p.Thr904=) c.2579C= (p.Thr860=) c.2501C= (p.Thr834=) n.3021C= | |
| 5 | g.56882190C>G | CA119079915 | MAP3K1 | c.2990C>G (p.Thr997Ser) c.2612C>G (p.Thr871Ser) c.2735C>G (p.Thr912Ser) c.2711C>G (p.Thr904Ser) c.2579C>G (p.Thr860Ser) c.2501C>G (p.Thr834Ser) n.3021C>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.56882190C>T | CA359787419 | MAP3K1 | c.2990C>T (p.Thr997Ile) c.2612C>T (p.Thr871Ile) c.2735C>T (p.Thr912Ile) c.2711C>T (p.Thr904Ile) c.2579C>T (p.Thr860Ile) c.2501C>T (p.Thr834Ile) n.3021C>T | dbSNP |
| 5 | g.56882191T>A | CA444399431 | MAP3K1 | c.2991T>A (p.Thr997=) c.2613T>A (p.Thr871=) c.2736T>A (p.Thr912=) c.2712T>A (p.Thr904=) c.2580T>A (p.Thr860=) c.2502T>A (p.Thr834=) n.3022T>A | |
| 5 | g.56882191T>C | CA444399433 | MAP3K1 | c.2991T>C (p.Thr997=) c.2613T>C (p.Thr871=) c.2736T>C (p.Thr912=) c.2712T>C (p.Thr904=) c.2580T>C (p.Thr860=) c.2502T>C (p.Thr834=) n.3022T>C | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.56882191T>G | CA444399432 | MAP3K1 | c.2991T>G (p.Thr997=) c.2613T>G (p.Thr871=) c.2736T>G (p.Thr912=) c.2712T>G (p.Thr904=) c.2580T>G (p.Thr860=) c.2502T>G (p.Thr834=) n.3022T>G | |
| 5 | g.56882191T= | CA1548139496 | MAP3K1 | c.2991T= (p.Thr997=) c.2613T= (p.Thr871=) c.2736T= (p.Thr912=) c.2712T= (p.Thr904=) c.2580T= (p.Thr860=) c.2502T= (p.Thr834=) n.3022T= | |
| 5 | g.56882192G>A | CA359787422 | MAP3K1 | c.2992G>A (p.Ala998Thr) c.2614G>A (p.Ala872Thr) c.2737G>A (p.Ala913Thr) c.2713G>A (p.Ala905Thr) c.2581G>A (p.Ala861Thr) c.2503G>A (p.Ala835Thr) n.3023G>A | dbSNP |
| 5 | g.56882192G>C | CA359787421 | MAP3K1 | c.2992G>C (p.Ala998Pro) c.2614G>C (p.Ala872Pro) c.2737G>C (p.Ala913Pro) c.2713G>C (p.Ala905Pro) c.2581G>C (p.Ala861Pro) c.2503G>C (p.Ala835Pro) n.3023G>C | dbSNP |
| 5 | g.56882192G>T | CA359787420 | MAP3K1 | c.2992G>T (p.Ala998Ser) c.2614G>T (p.Ala872Ser) c.2737G>T (p.Ala913Ser) c.2713G>T (p.Ala905Ser) c.2581G>T (p.Ala861Ser) c.2503G>T (p.Ala835Ser) n.3023G>T | |
| 5 | g.56882192_56882195delinsGCAA | CA1548139497 | MAP3K1 | c.2992_2995delinsGCAA (p.Ala998=) c.2614_2617delinsGCAA (p.Ala872=) c.2737_2740delinsGCAA (p.Ala913=) c.2713_2716delinsGCAA (p.Ala905=) c.2581_2584delinsGCAA (p.Ala861=) c.2503_2506delinsGCAA (p.Ala835=) n.3023_3026delinsGCAA | |
| 5 | g.56882193C>A | CA359787423 | MAP3K1 | c.2993C>A (p.Ala998Glu) c.2615C>A (p.Ala872Glu) c.2738C>A (p.Ala913Glu) c.2714C>A (p.Ala905Glu) c.2582C>A (p.Ala861Glu) c.2504C>A (p.Ala835Glu) n.3024C>A | dbSNP |
| 5 | g.56882193C= | CA1548139499 | MAP3K1 | c.2993C= (p.Ala998=) c.2615C= (p.Ala872=) c.2738C= (p.Ala913=) c.2714C= (p.Ala905=) c.2582C= (p.Ala861=) c.2504C= (p.Ala835=) n.3024C= | |
| 5 | g.56882193C>G | CA359787424 | MAP3K1 | c.2993C>G (p.Ala998Gly) c.2615C>G (p.Ala872Gly) c.2738C>G (p.Ala913Gly) c.2714C>G (p.Ala905Gly) c.2582C>G (p.Ala861Gly) c.2504C>G (p.Ala835Gly) n.3024C>G | dbSNP |
| 5 | g.56882193C>T | CA359787425 | MAP3K1 | c.2993C>T (p.Ala998Val) c.2615C>T (p.Ala872Val) c.2738C>T (p.Ala913Val) c.2714C>T (p.Ala905Val) c.2582C>T (p.Ala861Val) c.2504C>T (p.Ala835Val) n.3024C>T | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.56882193dup | CA645557021 | MAP3K1 | c.2993dup (p.Thr999AsnfsTer5) c.2615dup (p.Thr873AsnfsTer5) c.2738dup (p.Thr914AsnfsTer5) c.2714dup (p.Thr906AsnfsTer5) c.2582dup (p.Thr862AsnfsTer5) c.2504dup (p.Thr836AsnfsTer5) n.3024dup | COSMIC |
| 5 | g.56882195_56882197del | CA1548139498 | MAP3K1 | c.2995_2997del (p.Thr999del) c.2617_2619del (p.Thr873del) c.2740_2742del (p.Thr914del) c.2716_2718del (p.Thr906del) c.2584_2586del (p.Thr862del) c.2506_2508del (p.Thr836del) n.3026_3028del | dbSNP |
| 5 | g.56882194A>C | CA444399437 | MAP3K1 | c.2994A>C (p.Ala998=) c.2616A>C (p.Ala872=) c.2739A>C (p.Ala913=) c.2715A>C (p.Ala905=) c.2583A>C (p.Ala861=) c.2505A>C (p.Ala835=) n.3025A>C | |
| 5 | g.56882194A>G | CA444399438 | MAP3K1 | c.2994A>G (p.Ala998=) c.2616A>G (p.Ala872=) c.2739A>G (p.Ala913=) c.2715A>G (p.Ala905=) c.2583A>G (p.Ala861=) c.2505A>G (p.Ala835=) n.3025A>G | |
| 5 | g.56882194A>T | CA444399439 | MAP3K1 | c.2994A>T (p.Ala998=) c.2616A>T (p.Ala872=) c.2739A>T (p.Ala913=) c.2715A>T (p.Ala905=) c.2583A>T (p.Ala861=) c.2505A>T (p.Ala835=) n.3025A>T | dbSNP |
| 5 | g.56882195A>C | CA359787426 | MAP3K1 | c.2995A>C (p.Thr999Pro) c.2617A>C (p.Thr873Pro) c.2740A>C (p.Thr914Pro) c.2716A>C (p.Thr906Pro) c.2584A>C (p.Thr862Pro) c.2506A>C (p.Thr836Pro) n.3026A>C | |
| 5 | g.56882195A>G | CA359787427 | MAP3K1 | c.2995A>G (p.Thr999Ala) c.2617A>G (p.Thr873Ala) c.2740A>G (p.Thr914Ala) c.2716A>G (p.Thr906Ala) c.2584A>G (p.Thr862Ala) c.2506A>G (p.Thr836Ala) n.3026A>G | |
| 5 | g.56882195A>T | CA359787428 | MAP3K1 | c.2995A>T (p.Thr999Ser) c.2617A>T (p.Thr873Ser) c.2740A>T (p.Thr914Ser) c.2716A>T (p.Thr906Ser) c.2584A>T (p.Thr862Ser) c.2506A>T (p.Thr836Ser) n.3026A>T | dbSNP |
| 5 | g.56882196C>A | CA359787429 | MAP3K1 | c.2996C>A (p.Thr999Lys) c.2618C>A (p.Thr873Lys) c.2741C>A (p.Thr914Lys) c.2717C>A (p.Thr906Lys) c.2585C>A (p.Thr862Lys) c.2507C>A (p.Thr836Lys) n.3027C>A | dbSNP gnomAD v4 |
| 5 | g.56882196C>G | CA359787430 | MAP3K1 | c.2996C>G (p.Thr999Arg) c.2618C>G (p.Thr873Arg) c.2741C>G (p.Thr914Arg) c.2717C>G (p.Thr906Arg) c.2585C>G (p.Thr862Arg) c.2507C>G (p.Thr836Arg) n.3027C>G | |
| 5 | g.56882196C>T | CA359787431 | MAP3K1 | c.2996C>T (p.Thr999Ile) c.2618C>T (p.Thr873Ile) c.2741C>T (p.Thr914Ile) c.2717C>T (p.Thr906Ile) c.2585C>T (p.Thr862Ile) c.2507C>T (p.Thr836Ile) n.3027C>T | dbSNP gnomAD v4 |
| 5 | g.56882197A>C | CA444399444 | MAP3K1 | c.2997A>C (p.Thr999=) c.2619A>C (p.Thr873=) c.2742A>C (p.Thr914=) c.2718A>C (p.Thr906=) c.2586A>C (p.Thr862=) c.2508A>C (p.Thr836=) n.3028A>C |