| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.56882284A= | CA1548139540 | MAP3K1 | c.3084A= (p.Gln1028=) c.2706A= (p.Gln902=) c.2829A= (p.Gln943=) c.2805A= (p.Gln935=) c.2673A= (p.Gln891=) c.2595A= (p.Gln865=) n.3115A= | |
| 5 | g.56882284A>C | CA359787615 | MAP3K1 | c.3084A>C (p.Gln1028His) c.2706A>C (p.Gln902His) c.2829A>C (p.Gln943His) c.2805A>C (p.Gln935His) c.2673A>C (p.Gln891His) c.2595A>C (p.Gln865His) n.3115A>C | dbSNP |
| 5 | g.56882284A>G | CA3273115 | MAP3K1 | c.3084A>G (p.Gln1028=) c.2706A>G (p.Gln902=) c.2829A>G (p.Gln943=) c.2805A>G (p.Gln935=) c.2673A>G (p.Gln891=) c.2595A>G (p.Gln865=) n.3115A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.56882284A>T | CA359787616 | MAP3K1 | c.3084A>T (p.Gln1028His) c.2706A>T (p.Gln902His) c.2829A>T (p.Gln943His) c.2805A>T (p.Gln935His) c.2673A>T (p.Gln891His) c.2595A>T (p.Gln865His) n.3115A>T | dbSNP |
| 5 | g.56882285T>A | CA359787617 | MAP3K1 | c.3085T>A (p.Phe1029Ile) c.2707T>A (p.Phe903Ile) c.2830T>A (p.Phe944Ile) c.2806T>A (p.Phe936Ile) c.2674T>A (p.Phe892Ile) c.2596T>A (p.Phe866Ile) n.3116T>A | |
| 5 | g.56882285T>C | CA359787618 | MAP3K1 | c.3085T>C (p.Phe1029Leu) c.2707T>C (p.Phe903Leu) c.2830T>C (p.Phe944Leu) c.2806T>C (p.Phe936Leu) c.2674T>C (p.Phe892Leu) c.2596T>C (p.Phe866Leu) n.3116T>C | |
| 5 | g.56882285T>G | CA359787619 | MAP3K1 | c.3085T>G (p.Phe1029Val) c.2707T>G (p.Phe903Val) c.2830T>G (p.Phe944Val) c.2806T>G (p.Phe936Val) c.2674T>G (p.Phe892Val) c.2596T>G (p.Phe866Val) n.3116T>G | |
| 5 | g.56882286T>A | CA359787620 | MAP3K1 | c.3086T>A (p.Phe1029Tyr) c.2708T>A (p.Phe903Tyr) c.2831T>A (p.Phe944Tyr) c.2807T>A (p.Phe936Tyr) c.2675T>A (p.Phe892Tyr) c.2597T>A (p.Phe866Tyr) n.3117T>A | |
| 5 | g.56882286T>C | CA359787621 | MAP3K1 | c.3086T>C (p.Phe1029Ser) c.2708T>C (p.Phe903Ser) c.2831T>C (p.Phe944Ser) c.2807T>C (p.Phe936Ser) c.2675T>C (p.Phe892Ser) c.2597T>C (p.Phe866Ser) n.3117T>C | |
| 5 | g.56882286T>G | CA359787622 | MAP3K1 | c.3086T>G (p.Phe1029Cys) c.2708T>G (p.Phe903Cys) c.2831T>G (p.Phe944Cys) c.2807T>G (p.Phe936Cys) c.2675T>G (p.Phe892Cys) c.2597T>G (p.Phe866Cys) n.3117T>G | gnomAD v4 |
| 5 | g.56882287C>A | CA359787623 | MAP3K1 | c.3087C>A (p.Phe1029Leu) c.2709C>A (p.Phe903Leu) c.2832C>A (p.Phe944Leu) c.2808C>A (p.Phe936Leu) c.2676C>A (p.Phe892Leu) c.2598C>A (p.Phe866Leu) n.3118C>A | dbSNP |
| 5 | g.56882287C= | CA1548139541 | MAP3K1 | c.3087C= (p.Phe1029=) c.2709C= (p.Phe903=) c.2832C= (p.Phe944=) c.2808C= (p.Phe936=) c.2676C= (p.Phe892=) c.2598C= (p.Phe866=) n.3118C= | |
| 5 | g.56882287C>G | CA359787624 | MAP3K1 | c.3087C>G (p.Phe1029Leu) c.2709C>G (p.Phe903Leu) c.2832C>G (p.Phe944Leu) c.2808C>G (p.Phe936Leu) c.2676C>G (p.Phe892Leu) c.2598C>G (p.Phe866Leu) n.3118C>G | dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.56882287C>T | CA3273116 | MAP3K1 | c.3087C>T (p.Phe1029=) c.2709C>T (p.Phe903=) c.2832C>T (p.Phe944=) c.2808C>T (p.Phe936=) c.2676C>T (p.Phe892=) c.2598C>T (p.Phe866=) n.3118C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.56882288C>A | CA359787625 | MAP3K1 | c.3088C>A (p.His1030Asn) c.2710C>A (p.His904Asn) c.2833C>A (p.His945Asn) c.2809C>A (p.His937Asn) c.2677C>A (p.His893Asn) c.2599C>A (p.His867Asn) n.3119C>A | dbSNP |
| 5 | g.56882288C>G | CA359787627 | MAP3K1 | c.3088C>G (p.His1030Asp) c.2710C>G (p.His904Asp) c.2833C>G (p.His945Asp) c.2809C>G (p.His937Asp) c.2677C>G (p.His893Asp) c.2599C>G (p.His867Asp) n.3119C>G | dbSNP gnomAD v4 |
| 5 | g.56882288C>T | CA359787626 | MAP3K1 | c.3088C>T (p.His1030Tyr) c.2710C>T (p.His904Tyr) c.2833C>T (p.His945Tyr) c.2809C>T (p.His937Tyr) c.2677C>T (p.His893Tyr) c.2599C>T (p.His867Tyr) n.3119C>T | COSMIC |
| 5 | g.56882289A= | CA1548139542 | MAP3K1 | c.3089A= (p.His1030=) c.2711A= (p.His904=) c.2834A= (p.His945=) c.2810A= (p.His937=) c.2678A= (p.His893=) c.2600A= (p.His867=) n.3120A= | |
| 5 | g.56882289A>C | CA359787628 | MAP3K1 | c.3089A>C (p.His1030Pro) c.2711A>C (p.His904Pro) c.2834A>C (p.His945Pro) c.2810A>C (p.His937Pro) c.2678A>C (p.His893Pro) c.2600A>C (p.His867Pro) n.3120A>C | dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.56882289A>G | CA119080067 | MAP3K1 | c.3089A>G (p.His1030Arg) c.2711A>G (p.His904Arg) c.2834A>G (p.His945Arg) c.2810A>G (p.His937Arg) c.2678A>G (p.His893Arg) c.2600A>G (p.His867Arg) n.3120A>G | dbSNP |
| 5 | g.56882289A>T | CA359787629 | MAP3K1 | c.3089A>T (p.His1030Leu) c.2711A>T (p.His904Leu) c.2834A>T (p.His945Leu) c.2810A>T (p.His937Leu) c.2678A>T (p.His893Leu) c.2600A>T (p.His867Leu) n.3120A>T | |
| 5 | g.56882290C>A | CA359787630 | MAP3K1 | c.3090C>A (p.His1030Gln) c.2712C>A (p.His904Gln) c.2835C>A (p.His945Gln) c.2811C>A (p.His937Gln) c.2679C>A (p.His893Gln) c.2601C>A (p.His867Gln) n.3121C>A | dbSNP |
| 5 | g.56882290C= | CA1548139543 | MAP3K1 | c.3090C= (p.His1030=) c.2712C= (p.His904=) c.2835C= (p.His945=) c.2811C= (p.His937=) c.2679C= (p.His893=) c.2601C= (p.His867=) n.3121C= | |
| 5 | g.56882290C>G | CA359787631 | MAP3K1 | c.3090C>G (p.His1030Gln) c.2712C>G (p.His904Gln) c.2835C>G (p.His945Gln) c.2811C>G (p.His937Gln) c.2679C>G (p.His893Gln) c.2601C>G (p.His867Gln) n.3121C>G | dbSNP gnomAD v2 |
| 5 | g.56882290C>T | CA444399691 | MAP3K1 | c.3090C>T (p.His1030=) c.2712C>T (p.His904=) c.2835C>T (p.His945=) c.2811C>T (p.His937=) c.2679C>T (p.His893=) c.2601C>T (p.His867=) n.3121C>T | dbSNP gnomAD v4 |
| 5 | g.56882291A>C | CA444399696 | MAP3K1 | c.3091A>C (p.Arg1031=) c.2713A>C (p.Arg905=) c.2836A>C (p.Arg946=) c.2812A>C (p.Arg938=) c.2680A>C (p.Arg894=) c.2602A>C (p.Arg868=) n.3122A>C | |
| 5 | g.56882291A>G | CA359787632 | MAP3K1 | c.3091A>G (p.Arg1031Gly) c.2713A>G (p.Arg905Gly) c.2836A>G (p.Arg946Gly) c.2812A>G (p.Arg938Gly) c.2680A>G (p.Arg894Gly) c.2602A>G (p.Arg868Gly) n.3122A>G | dbSNP |
| 5 | g.56882291A>T | CA359787633 | MAP3K1 | c.3091A>T (p.Arg1031Ter) c.2713A>T (p.Arg905Ter) c.2836A>T (p.Arg946Ter) c.2812A>T (p.Arg938Ter) c.2680A>T (p.Arg894Ter) c.2602A>T (p.Arg868Ter) n.3122A>T | dbSNP |
| 5 | g.56882292G>A | CA359787634 | MAP3K1 | c.3092G>A (p.Arg1031Lys) c.2714G>A (p.Arg905Lys) c.2837G>A (p.Arg946Lys) c.2813G>A (p.Arg938Lys) c.2681G>A (p.Arg894Lys) c.2603G>A (p.Arg868Lys) n.3123G>A | |
| 5 | g.56882292G>C | CA359787635 | MAP3K1 | c.3092G>C (p.Arg1031Thr) c.2714G>C (p.Arg905Thr) c.2837G>C (p.Arg946Thr) c.2813G>C (p.Arg938Thr) c.2681G>C (p.Arg894Thr) c.2603G>C (p.Arg868Thr) n.3123G>C | |
| 5 | g.56882292G>T | CA359787636 | MAP3K1 | c.3092G>T (p.Arg1031Ile) c.2714G>T (p.Arg905Ile) c.2837G>T (p.Arg946Ile) c.2813G>T (p.Arg938Ile) c.2681G>T (p.Arg894Ile) c.2603G>T (p.Arg868Ile) n.3123G>T | |
| 5 | g.56882293A>C | CA359787637 | MAP3K1 | c.3093A>C (p.Arg1031Ser) c.2715A>C (p.Arg905Ser) c.2838A>C (p.Arg946Ser) c.2814A>C (p.Arg938Ser) c.2682A>C (p.Arg894Ser) c.2604A>C (p.Arg868Ser) n.3124A>C | |
| 5 | g.56882293A>G | CA444399707 | MAP3K1 | c.3093A>G (p.Arg1031=) c.2715A>G (p.Arg905=) c.2838A>G (p.Arg946=) c.2814A>G (p.Arg938=) c.2682A>G (p.Arg894=) c.2604A>G (p.Arg868=) n.3124A>G | dbSNP |
| 5 | g.56882293A>T | CA359787638 | MAP3K1 | c.3093A>T (p.Arg1031Ser) c.2715A>T (p.Arg905Ser) c.2838A>T (p.Arg946Ser) c.2814A>T (p.Arg938Ser) c.2682A>T (p.Arg894Ser) c.2604A>T (p.Arg868Ser) n.3124A>T | dbSNP |
| 5 | g.56882294A= | CA1548139544 | MAP3K1 | c.3094A= (p.Asn1032=) c.2716A= (p.Asn906=) c.2839A= (p.Asn947=) c.2815A= (p.Asn939=) c.2683A= (p.Asn895=) c.2605A= (p.Asn869=) n.3125A= | |
| 5 | g.56882294A>C | CA3273117 | MAP3K1 | c.3094A>C (p.Asn1032His) c.2716A>C (p.Asn906His) c.2839A>C (p.Asn947His) c.2815A>C (p.Asn939His) c.2683A>C (p.Asn895His) c.2605A>C (p.Asn869His) n.3125A>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.56882294A>G | CA359787639 | MAP3K1 | c.3094A>G (p.Asn1032Asp) c.2716A>G (p.Asn906Asp) c.2839A>G (p.Asn947Asp) c.2815A>G (p.Asn939Asp) c.2683A>G (p.Asn895Asp) c.2605A>G (p.Asn869Asp) n.3125A>G | |
| 5 | g.56882294A>T | CA359787640 | MAP3K1 | c.3094A>T (p.Asn1032Tyr) c.2716A>T (p.Asn906Tyr) c.2839A>T (p.Asn947Tyr) c.2815A>T (p.Asn939Tyr) c.2683A>T (p.Asn895Tyr) c.2605A>T (p.Asn869Tyr) n.3125A>T | dbSNP |
| 5 | g.56882295A>C | CA359787641 | MAP3K1 | c.3095A>C (p.Asn1032Thr) c.2717A>C (p.Asn906Thr) c.2840A>C (p.Asn947Thr) c.2816A>C (p.Asn939Thr) c.2684A>C (p.Asn895Thr) c.2606A>C (p.Asn869Thr) n.3126A>C | |
| 5 | g.56882295A>G | CA359787642 | MAP3K1 | c.3095A>G (p.Asn1032Ser) c.2717A>G (p.Asn906Ser) c.2840A>G (p.Asn947Ser) c.2816A>G (p.Asn939Ser) c.2684A>G (p.Asn895Ser) c.2606A>G (p.Asn869Ser) n.3126A>G | dbSNP |
| 5 | g.56882295A>T | CA359787643 | MAP3K1 | c.3095A>T (p.Asn1032Ile) c.2717A>T (p.Asn906Ile) c.2840A>T (p.Asn947Ile) c.2816A>T (p.Asn939Ile) c.2684A>T (p.Asn895Ile) c.2606A>T (p.Asn869Ile) n.3126A>T | dbSNP |
| 5 | g.56882296C>A | CA359787644 | MAP3K1 | c.3096C>A (p.Asn1032Lys) c.2718C>A (p.Asn906Lys) c.2841C>A (p.Asn947Lys) c.2817C>A (p.Asn939Lys) c.2685C>A (p.Asn895Lys) c.2607C>A (p.Asn869Lys) n.3127C>A | dbSNP |
| 5 | g.56882296C= | CA1548139545 | MAP3K1 | c.3096C= (p.Asn1032=) c.2718C= (p.Asn906=) c.2841C= (p.Asn947=) c.2817C= (p.Asn939=) c.2685C= (p.Asn895=) c.2607C= (p.Asn869=) n.3127C= | |
| 5 | g.56882296C>G | CA359787645 | MAP3K1 | c.3096C>G (p.Asn1032Lys) c.2718C>G (p.Asn906Lys) c.2841C>G (p.Asn947Lys) c.2817C>G (p.Asn939Lys) c.2685C>G (p.Asn895Lys) c.2607C>G (p.Asn869Lys) n.3127C>G | dbSNP gnomAD v4 |
| 5 | g.56882296C>T | CA3273118 | MAP3K1 | c.3096C>T (p.Asn1032=) c.2718C>T (p.Asn906=) c.2841C>T (p.Asn947=) c.2817C>T (p.Asn939=) c.2685C>T (p.Asn895=) c.2607C>T (p.Asn869=) n.3127C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.56882297T>A | CA359787646 | MAP3K1 | c.3097T>A (p.Cys1033Ser) c.2719T>A (p.Cys907Ser) c.2842T>A (p.Cys948Ser) c.2818T>A (p.Cys940Ser) c.2686T>A (p.Cys896Ser) c.2608T>A (p.Cys870Ser) n.3128T>A | |
| 5 | g.56882297T>C | CA359787647 | MAP3K1 | c.3097T>C (p.Cys1033Arg) c.2719T>C (p.Cys907Arg) c.2842T>C (p.Cys948Arg) c.2818T>C (p.Cys940Arg) c.2686T>C (p.Cys896Arg) c.2608T>C (p.Cys870Arg) n.3128T>C | dbSNP |
| 5 | g.56882297T>G | CA359787648 | MAP3K1 | c.3097T>G (p.Cys1033Gly) c.2719T>G (p.Cys907Gly) c.2842T>G (p.Cys948Gly) c.2818T>G (p.Cys940Gly) c.2686T>G (p.Cys896Gly) c.2608T>G (p.Cys870Gly) n.3128T>G | dbSNP |
| 5 | g.56882298G>A | CA359787649 | MAP3K1 | c.3098G>A (p.Cys1033Tyr) c.2720G>A (p.Cys907Tyr) c.2843G>A (p.Cys948Tyr) c.2819G>A (p.Cys940Tyr) c.2687G>A (p.Cys896Tyr) c.2609G>A (p.Cys870Tyr) n.3129G>A | dbSNP gnomAD v4 |
| 5 | g.56882298G>C | CA359787650 | MAP3K1 | c.3098G>C (p.Cys1033Ser) c.2720G>C (p.Cys907Ser) c.2843G>C (p.Cys948Ser) c.2819G>C (p.Cys940Ser) c.2687G>C (p.Cys896Ser) c.2609G>C (p.Cys870Ser) n.3129G>C | dbSNP |