Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.56882191T>ACA444399431MAP3K1c.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
5g.56882191T>CCA444399433MAP3K1c.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
5g.56882191T>GCA444399432MAP3K1c.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
5g.56882191T=CA1548139496MAP3K1c.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=
5g.56882192G>ACA359787422MAP3K1c.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
5g.56882192G>CCA359787421MAP3K1c.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
5g.56882192G>TCA359787420MAP3K1c.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
5g.56882192_56882195delinsGCAACA1548139497MAP3K1c.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
5g.56882193C>ACA359787423MAP3K1c.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
5g.56882193C=CA1548139499MAP3K1c.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=
5g.56882193C>GCA359787424MAP3K1c.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
5g.56882193C>TCA359787425MAP3K1c.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
5g.56882193dupCA645557021MAP3K1c.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
5g.56882195_56882197delCA1548139498MAP3K1c.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
5g.56882194A>CCA444399437MAP3K1c.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
5g.56882194A>GCA444399438MAP3K1c.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
5g.56882194A>TCA444399439MAP3K1c.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
5g.56882195A>CCA359787426MAP3K1c.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
5g.56882195A>GCA359787427MAP3K1c.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
5g.56882195A>TCA359787428MAP3K1c.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
5g.56882196C>ACA359787429MAP3K1c.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
5g.56882196C>GCA359787430MAP3K1c.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
5g.56882196C>TCA359787431MAP3K1c.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
5g.56882197A>CCA444399444MAP3K1c.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
5g.56882197A>GCA444399446MAP3K1c.2997A>G (p.Thr999=)
c.2619A>G (p.Thr873=)
c.2742A>G (p.Thr914=)
c.2718A>G (p.Thr906=)
c.2586A>G (p.Thr862=)
c.2508A>G (p.Thr836=)
n.3028A>G
5g.56882197A>TCA444399447MAP3K1c.2997A>T (p.Thr999=)
c.2619A>T (p.Thr873=)
c.2742A>T (p.Thr914=)
c.2718A>T (p.Thr906=)
c.2586A>T (p.Thr862=)
c.2508A>T (p.Thr836=)
n.3028A>T
 dbSNP
5g.56882197_56882200delCA645557022MAP3K1c.2997_3000del (p.Asp1000SerfsTer?)
c.2619_2622del (p.Asp874SerfsTer?)
c.2742_2745del (p.Asp915SerfsTer?)
c.2718_2721del (p.Asp907SerfsTer?)
c.2586_2589del (p.Asp863SerfsTer?)
c.2508_2511del (p.Asp837SerfsTer?)
n.3028_3031del
 COSMIC
5g.56882198G>ACA359787432MAP3K1c.2998G>A (p.Asp1000Asn)
c.2620G>A (p.Asp874Asn)
c.2743G>A (p.Asp915Asn)
c.2719G>A (p.Asp907Asn)
c.2587G>A (p.Asp863Asn)
c.2509G>A (p.Asp837Asn)
n.3029G>A
 dbSNP
5g.56882198G>CCA359787433MAP3K1c.2998G>C (p.Asp1000His)
c.2620G>C (p.Asp874His)
c.2743G>C (p.Asp915His)
c.2719G>C (p.Asp907His)
c.2587G>C (p.Asp863His)
c.2509G>C (p.Asp837His)
n.3029G>C
 dbSNP
5g.56882198G>TCA359787434MAP3K1c.2998G>T (p.Asp1000Tyr)
c.2620G>T (p.Asp874Tyr)
c.2743G>T (p.Asp915Tyr)
c.2719G>T (p.Asp907Tyr)
c.2587G>T (p.Asp863Tyr)
c.2509G>T (p.Asp837Tyr)
n.3029G>T
 dbSNP
5g.56882199A>CCA359787437MAP3K1c.2999A>C (p.Asp1000Ala)
c.2621A>C (p.Asp874Ala)
c.2744A>C (p.Asp915Ala)
c.2720A>C (p.Asp907Ala)
c.2588A>C (p.Asp863Ala)
c.2510A>C (p.Asp837Ala)
n.3030A>C
5g.56882199A>GCA359787436MAP3K1c.2999A>G (p.Asp1000Gly)
c.2621A>G (p.Asp874Gly)
c.2744A>G (p.Asp915Gly)
c.2720A>G (p.Asp907Gly)
c.2588A>G (p.Asp863Gly)
c.2510A>G (p.Asp837Gly)
n.3030A>G
5g.56882199A>TCA359787435MAP3K1c.2999A>T (p.Asp1000Val)
c.2621A>T (p.Asp874Val)
c.2744A>T (p.Asp915Val)
c.2720A>T (p.Asp907Val)
c.2588A>T (p.Asp863Val)
c.2510A>T (p.Asp837Val)
n.3030A>T
 dbSNP
5g.56882200T>ACA359787438MAP3K1c.3000T>A (p.Asp1000Glu)
c.2622T>A (p.Asp874Glu)
c.2745T>A (p.Asp915Glu)
c.2721T>A (p.Asp907Glu)
c.2589T>A (p.Asp863Glu)
c.2511T>A (p.Asp837Glu)
n.3031T>A
 dbSNP
5g.56882200T>CCA3273099MAP3K1c.3000T>C (p.Asp1000=)
c.2622T>C (p.Asp874=)
c.2745T>C (p.Asp915=)
c.2721T>C (p.Asp907=)
c.2589T>C (p.Asp863=)
c.2511T>C (p.Asp837=)
n.3031T>C
 dbSNP ExAC gnomAD v2 gnomAD v4
5g.56882200T>GCA359787439MAP3K1c.3000T>G (p.Asp1000Glu)
c.2622T>G (p.Asp874Glu)
c.2745T>G (p.Asp915Glu)
c.2721T>G (p.Asp907Glu)
c.2589T>G (p.Asp863Glu)
c.2511T>G (p.Asp837Glu)
n.3031T>G
5g.56882200T=CA1548139500MAP3K1c.3000T= (p.Asp1000=)
c.2622T= (p.Asp874=)
c.2745T= (p.Asp915=)
c.2721T= (p.Asp907=)
c.2589T= (p.Asp863=)
c.2511T= (p.Asp837=)
n.3031T=
5g.56882201G>ACA119079931MAP3K1c.3001G>A (p.Val1001Ile)
c.2623G>A (p.Val875Ile)
c.2746G>A (p.Val916Ile)
c.2722G>A (p.Val908Ile)
c.2590G>A (p.Val864Ile)
c.2512G>A (p.Val838Ile)
n.3032G>A
 dbSNP gnomAD v3 gnomAD v4
5g.56882201G>CCA359787440MAP3K1c.3001G>C (p.Val1001Leu)
c.2623G>C (p.Val875Leu)
c.2746G>C (p.Val916Leu)
c.2722G>C (p.Val908Leu)
c.2590G>C (p.Val864Leu)
c.2512G>C (p.Val838Leu)
n.3032G>C
 dbSNP gnomAD v4
5g.56882201G=CA1548139501MAP3K1c.3001G= (p.Val1001=)
c.2623G= (p.Val875=)
c.2746G= (p.Val916=)
c.2722G= (p.Val908=)
c.2590G= (p.Val864=)
c.2512G= (p.Val838=)
n.3032G=
5g.56882201G>TCA359787441MAP3K1c.3001G>T (p.Val1001Phe)
c.2623G>T (p.Val875Phe)
c.2746G>T (p.Val916Phe)
c.2722G>T (p.Val908Phe)
c.2590G>T (p.Val864Phe)
c.2512G>T (p.Val838Phe)
n.3032G>T
5g.56882202T>ACA359787442MAP3K1c.3002T>A (p.Val1001Asp)
c.2624T>A (p.Val875Asp)
c.2747T>A (p.Val916Asp)
c.2723T>A (p.Val908Asp)
c.2591T>A (p.Val864Asp)
c.2513T>A (p.Val838Asp)
n.3033T>A
5g.56882202T>CCA359787443MAP3K1c.3002T>C (p.Val1001Ala)
c.2624T>C (p.Val875Ala)
c.2747T>C (p.Val916Ala)
c.2723T>C (p.Val908Ala)
c.2591T>C (p.Val864Ala)
c.2513T>C (p.Val838Ala)
n.3033T>C
 gnomAD v4
5g.56882202T>GCA359787444MAP3K1c.3002T>G (p.Val1001Gly)
c.2624T>G (p.Val875Gly)
c.2747T>G (p.Val916Gly)
c.2723T>G (p.Val908Gly)
c.2591T>G (p.Val864Gly)
c.2513T>G (p.Val838Gly)
n.3033T>G
 gnomAD v4
5g.56882203C>ACA444399457MAP3K1c.3003C>A (p.Val1001=)
c.2625C>A (p.Val875=)
c.2748C>A (p.Val916=)
c.2724C>A (p.Val908=)
c.2592C>A (p.Val864=)
c.2514C>A (p.Val838=)
n.3034C>A
5g.56882203C>GCA444399461MAP3K1c.3003C>G (p.Val1001=)
c.2625C>G (p.Val875=)
c.2748C>G (p.Val916=)
c.2724C>G (p.Val908=)
c.2592C>G (p.Val864=)
c.2514C>G (p.Val838=)
n.3034C>G
 dbSNP
5g.56882203C>TCA444399463MAP3K1c.3003C>T (p.Val1001=)
c.2625C>T (p.Val875=)
c.2748C>T (p.Val916=)
c.2724C>T (p.Val908=)
c.2592C>T (p.Val864=)
c.2514C>T (p.Val838=)
n.3034C>T
 dbSNP gnomAD v4
5g.56882204T>ACA359787445MAP3K1c.3004T>A (p.Ser1002Thr)
c.2626T>A (p.Ser876Thr)
c.2749T>A (p.Ser917Thr)
c.2725T>A (p.Ser909Thr)
c.2593T>A (p.Ser865Thr)
c.2515T>A (p.Ser839Thr)
n.3035T>A
 dbSNP
5g.56882204T>CCA359787446MAP3K1c.3004T>C (p.Ser1002Pro)
c.2626T>C (p.Ser876Pro)
c.2749T>C (p.Ser917Pro)
c.2725T>C (p.Ser909Pro)
c.2593T>C (p.Ser865Pro)
c.2515T>C (p.Ser839Pro)
n.3035T>C
5g.56882204T>GCA359787447MAP3K1c.3004T>G (p.Ser1002Ala)
c.2626T>G (p.Ser876Ala)
c.2749T>G (p.Ser917Ala)
c.2725T>G (p.Ser909Ala)
c.2593T>G (p.Ser865Ala)
c.2515T>G (p.Ser839Ala)
n.3035T>G

Number of alleles fetched