Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.7141695A= | CA2320775558 | INSR | c.2664T= (p.Tyr888=) c.2628T= (p.Tyr876=) n.347T= c.2742T= (p.Tyr914=) c.2706T= (p.Tyr902=) | |
19 | g.7141695A>C | CA403661623 | INSR | c.2664T>G (p.Tyr888Ter) c.2628T>G (p.Tyr876Ter) n.347T>G c.2742T>G (p.Tyr914Ter) c.2706T>G (p.Tyr902Ter) | |
19 | g.7141695A>G | CA505193472 | INSR | c.2664T>C (p.Tyr888=) c.2628T>C (p.Tyr876=) n.347T>C c.2742T>C (p.Tyr914=) c.2706T>C (p.Tyr902=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7141695A>T | CA403661624 | INSR | c.2664T>A (p.Tyr888Ter) c.2628T>A (p.Tyr876Ter) n.347T>A c.2742T>A (p.Tyr914Ter) c.2706T>A (p.Tyr902Ter) | |
19 | g.7141696T>A | CA403661627 | INSR | c.2663A>T (p.Tyr888Phe) c.2627A>T (p.Tyr876Phe) n.346A>T c.2741A>T (p.Tyr914Phe) c.2705A>T (p.Tyr902Phe) | |
19 | g.7141696T>C | CA403661628 | INSR | c.2663A>G (p.Tyr888Cys) c.2627A>G (p.Tyr876Cys) n.346A>G c.2741A>G (p.Tyr914Cys) c.2705A>G (p.Tyr902Cys) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.7141696T>G | CA403661630 | INSR | c.2663A>C (p.Tyr888Ser) c.2627A>C (p.Tyr876Ser) n.346A>C c.2741A>C (p.Tyr914Ser) c.2705A>C (p.Tyr902Ser) | |
19 | g.7141696T= | CA2320775559 | INSR | c.2663A= (p.Tyr888=) c.2627A= (p.Tyr876=) n.346A= c.2741A= (p.Tyr914=) c.2705A= (p.Tyr902=) | |
19 | g.7141697A>C | CA403661636 | INSR | c.2662T>G (p.Tyr888Asp) c.2626T>G (p.Tyr876Asp) n.345T>G c.2740T>G (p.Tyr914Asp) c.2704T>G (p.Tyr902Asp) | |
19 | g.7141697A>G | CA403661634 | INSR | c.2662T>C (p.Tyr888His) c.2626T>C (p.Tyr876His) n.345T>C c.2740T>C (p.Tyr914His) c.2704T>C (p.Tyr902His) | |
19 | g.7141697A>T | CA403661633 | INSR | c.2662T>A (p.Tyr888Asn) c.2626T>A (p.Tyr876Asn) n.345T>A c.2740T>A (p.Tyr914Asn) c.2704T>A (p.Tyr902Asn) | |
19 | g.7141698A>C | CA403661638 | INSR | c.2661T>G (p.Ser887Arg) c.2625T>G (p.Ser875Arg) n.344T>G c.2739T>G (p.Ser913Arg) c.2703T>G (p.Ser901Arg) | |
19 | g.7141698A>G | CA505193473 | INSR | c.2661T>C (p.Ser887=) c.2625T>C (p.Ser875=) n.344T>C c.2739T>C (p.Ser913=) c.2703T>C (p.Ser901=) | |
19 | g.7141698A>T | CA403661640 | INSR | c.2661T>A (p.Ser887Arg) c.2625T>A (p.Ser875Arg) n.344T>A c.2739T>A (p.Ser913Arg) c.2703T>A (p.Ser901Arg) | |
19 | g.7141699C>A | CA403661643 | INSR | c.2660G>T (p.Ser887Ile) c.2624G>T (p.Ser875Ile) n.343G>T c.2738G>T (p.Ser913Ile) c.2702G>T (p.Ser901Ile) | |
19 | g.7141699C>G | CA403661644 | INSR | c.2660G>C (p.Ser887Thr) c.2624G>C (p.Ser875Thr) n.343G>C c.2738G>C (p.Ser913Thr) c.2702G>C (p.Ser901Thr) | |
19 | g.7141699C>T | CA403661647 | INSR | c.2660G>A (p.Ser887Asn) c.2624G>A (p.Ser875Asn) n.343G>A c.2738G>A (p.Ser913Asn) c.2702G>A (p.Ser901Asn) | |
19 | g.7141700T>A | CA403661649 | INSR | c.2659A>T (p.Ser887Cys) c.2623A>T (p.Ser875Cys) n.342A>T c.2737A>T (p.Ser913Cys) c.2701A>T (p.Ser901Cys) | |
19 | g.7141700T>C | CA403661651 | INSR | c.2659A>G (p.Ser887Gly) c.2623A>G (p.Ser875Gly) n.342A>G c.2737A>G (p.Ser913Gly) c.2701A>G (p.Ser901Gly) | |
19 | g.7141700T>G | CA403661653 | INSR | c.2659A>C (p.Ser887Arg) c.2623A>C (p.Ser875Arg) n.342A>C c.2737A>C (p.Ser913Arg) c.2701A>C (p.Ser901Arg) | |
19 | g.7141701C>A | CA505193476 | INSR | c.2658G>T (p.Val886=) c.2622G>T (p.Val874=) n.341G>T c.2736G>T (p.Val912=) c.2700G>T (p.Val900=) | |
19 | g.7141701C>G | CA505193475 | INSR | c.2658G>C (p.Val886=) c.2622G>C (p.Val874=) n.341G>C c.2736G>C (p.Val912=) c.2700G>C (p.Val900=) | |
19 | g.7141701C>T | CA505193474 | INSR | c.2658G>A (p.Val886=) c.2622G>A (p.Val874=) n.341G>A c.2736G>A (p.Val912=) c.2700G>A (p.Val900=) | |
19 | g.7141702A>C | CA403661654 | INSR | c.2657T>G (p.Val886Gly) c.2621T>G (p.Val874Gly) n.340T>G c.2735T>G (p.Val912Gly) c.2699T>G (p.Val900Gly) | gnomAD v4 |
19 | g.7141702A>G | CA403661655 | INSR | c.2657T>C (p.Val886Ala) c.2621T>C (p.Val874Ala) n.340T>C c.2735T>C (p.Val912Ala) c.2699T>C (p.Val900Ala) | |
19 | g.7141702A>T | CA403661658 | INSR | c.2657T>A (p.Val886Glu) c.2621T>A (p.Val874Glu) n.340T>A c.2735T>A (p.Val912Glu) c.2699T>A (p.Val900Glu) | |
19 | g.7141703C>A | CA403661660 | INSR | c.2656G>T (p.Val886Leu) c.2620G>T (p.Val874Leu) n.339G>T c.2734G>T (p.Val912Leu) c.2698G>T (p.Val900Leu) | |
19 | g.7141703C>G | CA403661662 | INSR | c.2656G>C (p.Val886Leu) c.2620G>C (p.Val874Leu) n.339G>C c.2734G>C (p.Val912Leu) c.2698G>C (p.Val900Leu) | |
19 | g.7141703C>T | CA403661664 | INSR | c.2656G>A (p.Val886Met) c.2620G>A (p.Val874Met) n.339G>A c.2734G>A (p.Val912Met) c.2698G>A (p.Val900Met) | |
19 | g.7141704T>A | CA403661666 | INSR | c.2655A>T (p.Glu885Asp) c.2619A>T (p.Glu873Asp) n.338A>T c.2733A>T (p.Glu911Asp) c.2697A>T (p.Glu899Asp) | |
19 | g.7141704T>C | CA505193477 | INSR | c.2655A>G (p.Glu885=) c.2619A>G (p.Glu873=) n.338A>G c.2733A>G (p.Glu911=) c.2697A>G (p.Glu899=) | gnomAD v4 |
19 | g.7141704T>G | CA403661668 | INSR | c.2655A>C (p.Glu885Asp) c.2619A>C (p.Glu873Asp) n.338A>C c.2733A>C (p.Glu911Asp) c.2697A>C (p.Glu899Asp) | |
19 | g.7141705T>A | CA403661670 | INSR | c.2654A>T (p.Glu885Val) c.2618A>T (p.Glu873Val) n.337A>T c.2732A>T (p.Glu911Val) c.2696A>T (p.Glu899Val) | |
19 | g.7141705T>C | CA403661672 | INSR | c.2654A>G (p.Glu885Gly) c.2618A>G (p.Glu873Gly) n.337A>G c.2732A>G (p.Glu911Gly) c.2696A>G (p.Glu899Gly) | |
19 | g.7141705T>G | CA403661674 | INSR | c.2654A>C (p.Glu885Ala) c.2618A>C (p.Glu873Ala) n.337A>C c.2732A>C (p.Glu911Ala) c.2696A>C (p.Glu899Ala) | |
19 | g.7141706C>A | CA403661676 | INSR | c.2653G>T (p.Glu885Ter) c.2617G>T (p.Glu873Ter) n.336G>T c.2731G>T (p.Glu911Ter) c.2695G>T (p.Glu899Ter) | |
19 | g.7141706C= | CA2320775560 | INSR | c.2653G= (p.Glu885=) c.2617G= (p.Glu873=) n.336G= c.2731G= (p.Glu911=) c.2695G= (p.Glu899=) | |
19 | g.7141706C>G | CA403661677 | INSR | c.2653G>C (p.Glu885Gln) c.2617G>C (p.Glu873Gln) n.336G>C c.2731G>C (p.Glu911Gln) c.2695G>C (p.Glu899Gln) | |
19 | g.7141706C>T | CA403661679 | INSR | c.2653G>A (p.Glu885Lys) c.2617G>A (p.Glu873Lys) n.336G>A c.2731G>A (p.Glu911Lys) c.2695G>A (p.Glu899Lys) | dbSNP |
19 | g.7141707A= | CA2320775561 | INSR | c.2652T= (p.Tyr884=) c.2616T= (p.Tyr872=) n.335T= c.2730T= (p.Tyr910=) c.2694T= (p.Tyr898=) | |
19 | g.7141707A>C | CA403661681 | INSR | c.2652T>G (p.Tyr884Ter) c.2616T>G (p.Tyr872Ter) n.335T>G c.2730T>G (p.Tyr910Ter) c.2694T>G (p.Tyr898Ter) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.7141707A>G | CA505193478 | INSR | c.2652T>C (p.Tyr884=) c.2616T>C (p.Tyr872=) n.335T>C c.2730T>C (p.Tyr910=) c.2694T>C (p.Tyr898=) | |
19 | g.7141707A>T | CA403661682 | INSR | c.2652T>A (p.Tyr884Ter) c.2616T>A (p.Tyr872Ter) n.335T>A c.2730T>A (p.Tyr910Ter) c.2694T>A (p.Tyr898Ter) | |
19 | g.7141708T>A | CA403661685 | INSR | c.2651A>T (p.Tyr884Phe) c.2615A>T (p.Tyr872Phe) n.334A>T c.2729A>T (p.Tyr910Phe) c.2693A>T (p.Tyr898Phe) | |
19 | g.7141708T>C | CA403661686 | INSR | c.2651A>G (p.Tyr884Cys) c.2615A>G (p.Tyr872Cys) n.334A>G c.2729A>G (p.Tyr910Cys) c.2693A>G (p.Tyr898Cys) | |
19 | g.7141708T>G | CA403661687 | INSR | c.2651A>C (p.Tyr884Ser) c.2615A>C (p.Tyr872Ser) n.334A>C c.2729A>C (p.Tyr910Ser) c.2693A>C (p.Tyr898Ser) | |
19 | g.7141709A>C | CA403661693 | INSR | c.2650T>G (p.Tyr884Asp) c.2614T>G (p.Tyr872Asp) n.333T>G c.2728T>G (p.Tyr910Asp) c.2692T>G (p.Tyr898Asp) | |
19 | g.7141709A>G | CA403661691 | INSR | c.2650T>C (p.Tyr884His) c.2614T>C (p.Tyr872His) n.333T>C c.2728T>C (p.Tyr910His) c.2692T>C (p.Tyr898His) | |
19 | g.7141709A>T | CA403661689 | INSR | c.2650T>A (p.Tyr884Asn) c.2614T>A (p.Tyr872Asn) n.333T>A c.2728T>A (p.Tyr910Asn) c.2692T>A (p.Tyr898Asn) | |
19 | g.7141710C>A | CA505193479 | INSR | c.2649G>T (p.Leu883=) c.2613G>T (p.Leu871=) n.332G>T c.2727G>T (p.Leu909=) c.2691G>T (p.Leu897=) | |
19 | g.7141710C>G | CA505193480 | INSR | c.2649G>C (p.Leu883=) c.2613G>C (p.Leu871=) n.332G>C c.2727G>C (p.Leu909=) c.2691G>C (p.Leu897=) | |
19 | g.7141710C>T | CA505193481 | INSR | c.2649G>A (p.Leu883=) c.2613G>A (p.Leu871=) n.332G>A c.2727G>A (p.Leu909=) c.2691G>A (p.Leu897=) | |
19 | g.7141711A>C | CA403661695 | INSR | c.2648T>G (p.Leu883Arg) c.2612T>G (p.Leu871Arg) n.331T>G c.2726T>G (p.Leu909Arg) c.2690T>G (p.Leu897Arg) | |
19 | g.7141711A>G | CA403661699 | INSR | c.2648T>C (p.Leu883Pro) c.2612T>C (p.Leu871Pro) n.331T>C c.2726T>C (p.Leu909Pro) c.2690T>C (p.Leu897Pro) | |
19 | g.7141711A>T | CA403661697 | INSR | c.2648T>A (p.Leu883Gln) c.2612T>A (p.Leu871Gln) n.331T>A c.2726T>A (p.Leu909Gln) c.2690T>A (p.Leu897Gln) | |
19 | g.7141712G>A | CA505193482 | INSR | c.2647C>T (p.Leu883=) c.2611C>T (p.Leu871=) n.330C>T c.2725C>T (p.Leu909=) c.2689C>T (p.Leu897=) | |
19 | g.7141712G>C | CA403661700 | INSR | c.2647C>G (p.Leu883Val) c.2611C>G (p.Leu871Val) n.330C>G c.2725C>G (p.Leu909Val) c.2689C>G (p.Leu897Val) | |
19 | g.7141712G>T | CA403661701 | INSR | c.2647C>A (p.Leu883Met) c.2611C>A (p.Leu871Met) n.330C>A c.2725C>A (p.Leu909Met) c.2689C>A (p.Leu897Met) | |
19 | g.7141713C>A | CA505193485 | INSR | c.2646G>T (p.Val882=) c.2610G>T (p.Val870=) n.329G>T c.2724G>T (p.Val908=) c.2688G>T (p.Val896=) | |
19 | g.7141713C>G | CA505193483 | INSR | c.2646G>C (p.Val882=) c.2610G>C (p.Val870=) n.329G>C c.2724G>C (p.Val908=) c.2688G>C (p.Val896=) | |
19 | g.7141713C>T | CA505193484 | INSR | c.2646G>A (p.Val882=) c.2610G>A (p.Val870=) n.329G>A c.2724G>A (p.Val908=) c.2688G>A (p.Val896=) | |
19 | g.7141714A>C | CA403661702 | INSR | c.2645T>G (p.Val882Gly) c.2609T>G (p.Val870Gly) n.328T>G c.2723T>G (p.Val908Gly) c.2687T>G (p.Val896Gly) | |
19 | g.7141714A>G | CA403661703 | INSR | c.2645T>C (p.Val882Ala) c.2609T>C (p.Val870Ala) n.328T>C c.2723T>C (p.Val908Ala) c.2687T>C (p.Val896Ala) | |
19 | g.7141714A>T | CA403661704 | INSR | c.2645T>A (p.Val882Glu) c.2609T>A (p.Val870Glu) n.328T>A c.2723T>A (p.Val908Glu) c.2687T>A (p.Val896Glu) | |
19 | g.7141715C>A | CA403661705 | INSR | c.2644G>T (p.Val882Leu) c.2608G>T (p.Val870Leu) n.327G>T c.2722G>T (p.Val908Leu) c.2686G>T (p.Val896Leu) | |
19 | g.7141715C= | CA2320775562 | INSR | c.2644G= (p.Val882=) c.2608G= (p.Val870=) n.327G= c.2722G= (p.Val908=) c.2686G= (p.Val896=) | |
19 | g.7141715C>G | CA304836381 | INSR | c.2644G>C (p.Val882Leu) c.2608G>C (p.Val870Leu) n.327G>C c.2722G>C (p.Val908Leu) c.2686G>C (p.Val896Leu) | dbSNP |
19 | g.7141715C>T | CA9135497 | INSR | c.2644G>A (p.Val882Met) c.2608G>A (p.Val870Met) n.327G>A c.2722G>A (p.Val908Met) c.2686G>A (p.Val896Met) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
19 | g.7141716G>A | CA9135498 | INSR | c.2643C>T (p.Ile881=) c.2607C>T (p.Ile869=) n.326C>T c.2721C>T (p.Ile907=) c.2685C>T (p.Ile895=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7141716G>C | CA403661706 | INSR | c.2643C>G (p.Ile881Met) c.2607C>G (p.Ile869Met) n.326C>G c.2721C>G (p.Ile907Met) c.2685C>G (p.Ile895Met) | |
19 | g.7141716G= | CA2320775563 | INSR | c.2643C= (p.Ile881=) c.2607C= (p.Ile869=) n.326C= c.2721C= (p.Ile907=) c.2685C= (p.Ile895=) | |
19 | g.7141716G>T | CA505193486 | INSR | c.2643C>A (p.Ile881=) c.2607C>A (p.Ile869=) n.326C>A c.2721C>A (p.Ile907=) c.2685C>A (p.Ile895=) | gnomAD v4 |
19 | g.7141717A= | CA2320775564 | INSR | c.2642T= (p.Ile881=) c.2606T= (p.Ile869=) n.325T= c.2720T= (p.Ile907=) c.2684T= (p.Ile895=) | |
19 | g.7141717A>C | CA403661707 | INSR | c.2642T>G (p.Ile881Ser) c.2606T>G (p.Ile869Ser) n.325T>G c.2720T>G (p.Ile907Ser) c.2684T>G (p.Ile895Ser) | |
19 | g.7141717A>G | CA304836389 | INSR | c.2642T>C (p.Ile881Thr) c.2606T>C (p.Ile869Thr) n.325T>C c.2720T>C (p.Ile907Thr) c.2684T>C (p.Ile895Thr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7141717A>T | CA403661708 | INSR | c.2642T>A (p.Ile881Asn) c.2606T>A (p.Ile869Asn) n.325T>A c.2720T>A (p.Ile907Asn) c.2684T>A (p.Ile895Asn) | |
19 | g.7141717_7141729delinsTGAGT | CA2695228093 | INSR | c.2630_2642delinsACTCA (p.Pro877HisfsTer6) c.2594_2606delinsACTCA (p.Pro865HisfsTer6) n.313_325delinsACTCA c.2708_2720delinsACTCA (p.Pro903HisfsTer6) c.2672_2684delinsACTCA (p.Pro891HisfsTer6) | |
19 | g.7141718T>A | CA403661711 | INSR | c.2641A>T (p.Ile881Phe) c.2605A>T (p.Ile869Phe) n.324A>T c.2719A>T (p.Ile907Phe) c.2683A>T (p.Ile895Phe) | |
19 | g.7141718T>C | CA403661710 | INSR | c.2641A>G (p.Ile881Val) c.2605A>G (p.Ile869Val) n.324A>G c.2719A>G (p.Ile907Val) c.2683A>G (p.Ile895Val) | |
19 | g.7141718T>G | CA403661709 | INSR | c.2641A>C (p.Ile881Leu) c.2605A>C (p.Ile869Leu) n.324A>C c.2719A>C (p.Ile907Leu) c.2683A>C (p.Ile895Leu) | |
19 | g.7141719C>A | CA505193487 | INSR | c.2640G>T (p.Leu880=) c.2604G>T (p.Leu868=) n.323G>T c.2718G>T (p.Leu906=) c.2682G>T (p.Leu894=) | |
19 | g.7141719C>G | CA505193488 | INSR | c.2640G>C (p.Leu880=) c.2604G>C (p.Leu868=) n.323G>C c.2718G>C (p.Leu906=) c.2682G>C (p.Leu894=) | |
19 | g.7141719C>T | CA505193489 | INSR | c.2640G>A (p.Leu880=) c.2604G>A (p.Leu868=) n.323G>A c.2718G>A (p.Leu906=) c.2682G>A (p.Leu894=) | |
19 | g.7141720A>C | CA403661712 | INSR | c.2639T>G (p.Leu880Arg) c.2603T>G (p.Leu868Arg) n.322T>G c.2717T>G (p.Leu906Arg) c.2681T>G (p.Leu894Arg) | |
19 | g.7141720A>G | CA403661713 | INSR | c.2639T>C (p.Leu880Pro) c.2603T>C (p.Leu868Pro) n.322T>C c.2717T>C (p.Leu906Pro) c.2681T>C (p.Leu894Pro) | |
19 | g.7141720A>T | CA403661714 | INSR | c.2639T>A (p.Leu880Gln) c.2603T>A (p.Leu868Gln) n.322T>A c.2717T>A (p.Leu906Gln) c.2681T>A (p.Leu894Gln) | |
19 | g.7141721G>A | CA505193490 | INSR | c.2638C>T (p.Leu880=) c.2602C>T (p.Leu868=) n.321C>T c.2716C>T (p.Leu906=) c.2680C>T (p.Leu894=) | |
19 | g.7141721G>C | CA403661715 | INSR | c.2638C>G (p.Leu880Val) c.2602C>G (p.Leu868Val) n.321C>G c.2716C>G (p.Leu906Val) c.2680C>G (p.Leu894Val) | |
19 | g.7141721G>T | CA403661716 | INSR | c.2638C>A (p.Leu880Met) c.2602C>A (p.Leu868Met) n.321C>A c.2716C>A (p.Leu906Met) c.2680C>A (p.Leu894Met) | |
19 | g.7141722A>C | CA505193491 | INSR | c.2637T>G (p.Gly879=) c.2601T>G (p.Gly867=) n.320T>G c.2715T>G (p.Gly905=) c.2679T>G (p.Gly893=) | |
19 | g.7141722A>G | CA505193492 | INSR | c.2637T>C (p.Gly879=) c.2601T>C (p.Gly867=) n.320T>C c.2715T>C (p.Gly905=) c.2679T>C (p.Gly893=) | |
19 | g.7141722A>T | CA505193493 | INSR | c.2637T>A (p.Gly879=) c.2601T>A (p.Gly867=) n.320T>A c.2715T>A (p.Gly905=) c.2679T>A (p.Gly893=) | |
19 | g.7141723C>A | CA403661717 | INSR | c.2636G>T (p.Gly879Val) c.2600G>T (p.Gly867Val) n.319G>T c.2714G>T (p.Gly905Val) c.2678G>T (p.Gly893Val) | |
19 | g.7141723C>G | CA403661718 | INSR | c.2636G>C (p.Gly879Ala) c.2600G>C (p.Gly867Ala) n.319G>C c.2714G>C (p.Gly905Ala) c.2678G>C (p.Gly893Ala) | |
19 | g.7141723C>T | CA403661719 | INSR | c.2636G>A (p.Gly879Asp) c.2600G>A (p.Gly867Asp) n.319G>A c.2714G>A (p.Gly905Asp) c.2678G>A (p.Gly893Asp) | gnomAD v4 |
19 | g.7141724C>A | CA403661720 | INSR | c.2635G>T (p.Gly879Cys) c.2599G>T (p.Gly867Cys) n.318G>T c.2713G>T (p.Gly905Cys) c.2677G>T (p.Gly893Cys) | COSMIC COSMIC |
19 | g.7141724C>G | CA403661721 | INSR | c.2635G>C (p.Gly879Arg) c.2599G>C (p.Gly867Arg) n.318G>C c.2713G>C (p.Gly905Arg) c.2677G>C (p.Gly893Arg) | |
19 | g.7141724C>T | CA403661722 | INSR | c.2635G>A (p.Gly879Ser) c.2599G>A (p.Gly867Ser) n.318G>A c.2713G>A (p.Gly905Ser) c.2677G>A (p.Gly893Ser) | |
19 | g.7141725A>C | CA403661723 | INSR | c.2634T>G (p.Asn878Lys) c.2598T>G (p.Asn866Lys) n.317T>G c.2712T>G (p.Asn904Lys) c.2676T>G (p.Asn892Lys) | |
19 | g.7141725A>G | CA505193494 | INSR | c.2634T>C (p.Asn878=) c.2598T>C (p.Asn866=) n.317T>C c.2712T>C (p.Asn904=) c.2676T>C (p.Asn892=) | gnomAD v4 |
19 | g.7141725A>T | CA403661724 | INSR | c.2634T>A (p.Asn878Lys) c.2598T>A (p.Asn866Lys) n.317T>A c.2712T>A (p.Asn904Lys) c.2676T>A (p.Asn892Lys) | |
19 | g.7141726T>A | CA403661726 | INSR | c.2633A>T (p.Asn878Ile) c.2597A>T (p.Asn866Ile) n.316A>T c.2711A>T (p.Asn904Ile) c.2675A>T (p.Asn892Ile) | |
19 | g.7141726T>C | CA304836394 | INSR | c.2633A>G (p.Asn878Ser) c.2597A>G (p.Asn866Ser) n.316A>G c.2711A>G (p.Asn904Ser) c.2675A>G (p.Asn892Ser) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7141726T>G | CA403661725 | INSR | c.2633A>C (p.Asn878Thr) c.2597A>C (p.Asn866Thr) n.316A>C c.2711A>C (p.Asn904Thr) c.2675A>C (p.Asn892Thr) | |
19 | g.7141726T= | CA2320775565 | INSR | c.2633A= (p.Asn878=) c.2597A= (p.Asn866=) n.316A= c.2711A= (p.Asn904=) c.2675A= (p.Asn892=) | |
19 | g.7141727T>A | CA403661727 | INSR | c.2632A>T (p.Asn878Tyr) c.2596A>T (p.Asn866Tyr) n.315A>T c.2710A>T (p.Asn904Tyr) c.2674A>T (p.Asn892Tyr) | |
19 | g.7141727T>C | CA403661728 | INSR | c.2632A>G (p.Asn878Asp) c.2596A>G (p.Asn866Asp) n.315A>G c.2710A>G (p.Asn904Asp) c.2674A>G (p.Asn892Asp) | |
19 | g.7141727T>G | CA403661729 | INSR | c.2632A>C (p.Asn878His) c.2596A>C (p.Asn866His) n.315A>C c.2710A>C (p.Asn904His) c.2674A>C (p.Asn892His) | |
19 | g.7141728G>A | CA505193495 | INSR | c.2631C>T (p.Pro877=) c.2595C>T (p.Pro865=) n.314C>T c.2709C>T (p.Pro903=) c.2673C>T (p.Pro891=) | |
19 | g.7141728G>C | CA505193496 | INSR | c.2631C>G (p.Pro877=) c.2595C>G (p.Pro865=) n.314C>G c.2709C>G (p.Pro903=) c.2673C>G (p.Pro891=) | |
19 | g.7141728G>T | CA505193497 | INSR | c.2631C>A (p.Pro877=) c.2595C>A (p.Pro865=) n.314C>A c.2709C>A (p.Pro903=) c.2673C>A (p.Pro891=) | |
19 | g.7141729G>A | CA403661730 | INSR | c.2630C>T (p.Pro877Leu) c.2594C>T (p.Pro865Leu) n.313C>T c.2708C>T (p.Pro903Leu) c.2672C>T (p.Pro891Leu) | |
19 | g.7141729G>C | CA403661731 | INSR | c.2630C>G (p.Pro877Arg) c.2594C>G (p.Pro865Arg) n.313C>G c.2708C>G (p.Pro903Arg) c.2672C>G (p.Pro891Arg) | |
19 | g.7141729G>T | CA403661732 | INSR | c.2630C>A (p.Pro877His) c.2594C>A (p.Pro865His) n.313C>A c.2708C>A (p.Pro903His) c.2672C>A (p.Pro891His) | |
19 | g.7141730G>A | CA403661733 | INSR | c.2629C>T (p.Pro877Ser) c.2593C>T (p.Pro865Ser) n.312C>T c.2707C>T (p.Pro903Ser) c.2671C>T (p.Pro891Ser) | gnomAD v4 |
19 | g.7141730G>C | CA403661734 | INSR | c.2629C>G (p.Pro877Ala) c.2593C>G (p.Pro865Ala) n.312C>G c.2707C>G (p.Pro903Ala) c.2671C>G (p.Pro891Ala) | |
19 | g.7141730G>T | CA403661735 | INSR | c.2629C>A (p.Pro877Thr) c.2593C>A (p.Pro865Thr) n.312C>A c.2707C>A (p.Pro903Thr) c.2671C>A (p.Pro891Thr) | |
19 | g.7141731C>A | CA403661736 | INSR | c.2628G>T (p.Glu876Asp) c.2592G>T (p.Glu864Asp) n.311G>T c.2706G>T (p.Glu902Asp) c.2670G>T (p.Glu890Asp) | |
19 | g.7141731C>G | CA403661737 | INSR | c.2628G>C (p.Glu876Asp) c.2592G>C (p.Glu864Asp) n.311G>C c.2706G>C (p.Glu902Asp) c.2670G>C (p.Glu890Asp) | |
19 | g.7141731C>T | CA505193498 | INSR | c.2628G>A (p.Glu876=) c.2592G>A (p.Glu864=) n.311G>A c.2706G>A (p.Glu902=) c.2670G>A (p.Glu890=) | |
19 | g.7141732T>A | CA403661740 | INSR | c.2627A>T (p.Glu876Val) c.2591A>T (p.Glu864Val) n.310A>T c.2705A>T (p.Glu902Val) c.2669A>T (p.Glu890Val) | |
19 | g.7141732T>C | CA403661739 | INSR | c.2627A>G (p.Glu876Gly) c.2591A>G (p.Glu864Gly) n.310A>G c.2705A>G (p.Glu902Gly) c.2669A>G (p.Glu890Gly) | dbSNP |
19 | g.7141732T>G | CA403661738 | INSR | c.2627A>C (p.Glu876Ala) c.2591A>C (p.Glu864Ala) n.310A>C c.2705A>C (p.Glu902Ala) c.2669A>C (p.Glu890Ala) | |
19 | g.7141732T= | CA2320775566 | INSR | c.2627A= (p.Glu876=) c.2591A= (p.Glu864=) n.310A= c.2705A= (p.Glu902=) c.2669A= (p.Glu890=) | |
19 | g.7141733C>A | CA403661741 | INSR | c.2626G>T (p.Glu876Ter) c.2590G>T (p.Glu864Ter) n.309G>T c.2704G>T (p.Glu902Ter) c.2668G>T (p.Glu890Ter) | gnomAD v4 |
19 | g.7141733C>G | CA403661742 | INSR | c.2626G>C (p.Glu876Gln) c.2590G>C (p.Glu864Gln) n.309G>C c.2704G>C (p.Glu902Gln) c.2668G>C (p.Glu890Gln) | |
19 | g.7141733C>T | CA403661743 | INSR | c.2626G>A (p.Glu876Lys) c.2590G>A (p.Glu864Lys) n.309G>A c.2704G>A (p.Glu902Lys) c.2668G>A (p.Glu890Lys) | gnomAD v4 |
19 | g.7141734C>A | CA403661744 | INSR | c.2625G>T (p.Lys875Asn) c.2589G>T (p.Lys863Asn) n.308G>T c.2703G>T (p.Lys901Asn) c.2667G>T (p.Lys889Asn) | |
19 | g.7141734C>G | CA403661745 | INSR | c.2625G>C (p.Lys875Asn) c.2589G>C (p.Lys863Asn) n.308G>C c.2703G>C (p.Lys901Asn) c.2667G>C (p.Lys889Asn) | |
19 | g.7141734C>T | CA505193499 | INSR | c.2625G>A (p.Lys875=) c.2589G>A (p.Lys863=) n.308G>A c.2703G>A (p.Lys901=) c.2667G>A (p.Lys889=) | |
19 | g.7141735T>A | CA403661748 | INSR | c.2624A>T (p.Lys875Met) c.2588A>T (p.Lys863Met) n.307A>T c.2702A>T (p.Lys901Met) c.2666A>T (p.Lys889Met) | gnomAD v4 |
19 | g.7141735T>C | CA403661750 | INSR | c.2624A>G (p.Lys875Arg) c.2588A>G (p.Lys863Arg) n.307A>G c.2702A>G (p.Lys901Arg) c.2666A>G (p.Lys889Arg) | |
19 | g.7141735T>G | CA403661751 | INSR | c.2624A>C (p.Lys875Thr) c.2588A>C (p.Lys863Thr) n.307A>C c.2702A>C (p.Lys901Thr) c.2666A>C (p.Lys889Thr) | |
19 | g.7141736T>A | CA403661753 | INSR | c.2623A>T (p.Lys875Ter) c.2587A>T (p.Lys863Ter) n.306A>T c.2701A>T (p.Lys901Ter) c.2665A>T (p.Lys889Ter) | |
19 | g.7141736T>C | CA403661755 | INSR | c.2623A>G (p.Lys875Glu) c.2587A>G (p.Lys863Glu) n.306A>G c.2701A>G (p.Lys901Glu) c.2665A>G (p.Lys889Glu) | |
19 | g.7141736T>G | CA403661757 | INSR | c.2623A>C (p.Lys875Gln) c.2587A>C (p.Lys863Gln) n.306A>C c.2701A>C (p.Lys901Gln) c.2665A>C (p.Lys889Gln) | |
19 | g.7141737C>A | CA505193500 | INSR | c.2622G>T (p.Pro874=) c.2586G>T (p.Pro862=) n.305G>T c.2700G>T (p.Pro900=) c.2664G>T (p.Pro888=) | |
19 | g.7141737C= | CA2320775567 | INSR | c.2622G= (p.Pro874=) c.2586G= (p.Pro862=) n.305G= c.2700G= (p.Pro900=) c.2664G= (p.Pro888=) | |
19 | g.7141737C>G | CA505193501 | INSR | c.2622G>C (p.Pro874=) c.2586G>C (p.Pro862=) n.305G>C c.2700G>C (p.Pro900=) c.2664G>C (p.Pro888=) | gnomAD v4 |
19 | g.7141737C>T | CA9135499 | INSR | c.2622G>A (p.Pro874=) c.2586G>A (p.Pro862=) n.305G>A c.2700G>A (p.Pro900=) c.2664G>A (p.Pro888=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7141738G>A | CA403661764 | INSR | c.2621C>T (p.Pro874Leu) c.2585C>T (p.Pro862Leu) n.304C>T c.2699C>T (p.Pro900Leu) c.2663C>T (p.Pro888Leu) | gnomAD v4 COSMIC COSMIC |
19 | g.7141738G>C | CA403661762 | INSR | c.2621C>G (p.Pro874Arg) c.2585C>G (p.Pro862Arg) n.304C>G c.2699C>G (p.Pro900Arg) c.2663C>G (p.Pro888Arg) | |
19 | g.7141738G>T | CA403661760 | INSR | c.2621C>A (p.Pro874Gln) c.2585C>A (p.Pro862Gln) n.304C>A c.2699C>A (p.Pro900Gln) c.2663C>A (p.Pro888Gln) | |
19 | g.7141739G>A | CA403661765 | INSR | c.2620C>T (p.Pro874Ser) c.2584C>T (p.Pro862Ser) n.303C>T c.2698C>T (p.Pro900Ser) c.2662C>T (p.Pro888Ser) | |
19 | g.7141739G>C | CA403661769 | INSR | c.2620C>G (p.Pro874Ala) c.2584C>G (p.Pro862Ala) n.303C>G c.2698C>G (p.Pro900Ala) c.2662C>G (p.Pro888Ala) | |
19 | g.7141739G>T | CA403661767 | INSR | c.2620C>A (p.Pro874Thr) c.2584C>A (p.Pro862Thr) n.303C>A c.2698C>A (p.Pro900Thr) c.2662C>A (p.Pro888Thr) | |
19 | g.7141740C>A | CA403661771 | INSR | c.2619G>T (p.Glu873Asp) c.2583G>T (p.Glu861Asp) n.302G>T c.2697G>T (p.Glu899Asp) c.2661G>T (p.Glu887Asp) | |
19 | g.7141740C>G | CA403661773 | INSR | c.2619G>C (p.Glu873Asp) c.2583G>C (p.Glu861Asp) n.302G>C c.2697G>C (p.Glu899Asp) c.2661G>C (p.Glu887Asp) | |
19 | g.7141740C>T | CA505193502 | INSR | c.2619G>A (p.Glu873=) c.2583G>A (p.Glu861=) n.302G>A c.2697G>A (p.Glu899=) c.2661G>A (p.Glu887=) | gnomAD v4 |
19 | g.7141741T>A | CA403661775 | INSR | c.2618A>T (p.Glu873Val) c.2582A>T (p.Glu861Val) n.301A>T c.2696A>T (p.Glu899Val) c.2660A>T (p.Glu887Val) | |
19 | g.7141741T>C | CA9135500 | INSR | c.2618A>G (p.Glu873Gly) c.2582A>G (p.Glu861Gly) n.301A>G c.2696A>G (p.Glu899Gly) c.2660A>G (p.Glu887Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.7141741T>G | CA403661778 | INSR | c.2618A>C (p.Glu873Ala) c.2582A>C (p.Glu861Ala) n.301A>C c.2696A>C (p.Glu899Ala) c.2660A>C (p.Glu887Ala) | |
19 | g.7141741T= | CA2320775568 | INSR | c.2618A= (p.Glu873=) c.2582A= (p.Glu861=) n.301A= c.2696A= (p.Glu899=) c.2660A= (p.Glu887=) | |
19 | g.7141742C>A | CA403661780 | INSR | c.2617G>T (p.Glu873Ter) c.2581G>T (p.Glu861Ter) n.300G>T c.2695G>T (p.Glu899Ter) c.2659G>T (p.Glu887Ter) | |
19 | g.7141742C>G | CA403661782 | INSR | c.2617G>C (p.Glu873Gln) c.2581G>C (p.Glu861Gln) n.300G>C c.2695G>C (p.Glu899Gln) c.2659G>C (p.Glu887Gln) | COSMIC COSMIC |
19 | g.7141742C>T | CA403661784 | INSR | c.2617G>A (p.Glu873Lys) c.2581G>A (p.Glu861Lys) n.300G>A c.2695G>A (p.Glu899Lys) c.2659G>A (p.Glu887Lys) | |
19 | g.7141743C>A | CA403661786 | INSR | c.2616G>T (p.Gln872His) c.2580G>T (p.Gln860His) n.299G>T c.2694G>T (p.Gln898His) c.2658G>T (p.Gln886His) | |
19 | g.7141743C>G | CA403661788 | INSR | c.2616G>C (p.Gln872His) c.2580G>C (p.Gln860His) n.299G>C c.2694G>C (p.Gln898His) c.2658G>C (p.Gln886His) | |
19 | g.7141743C>T | CA505193503 | INSR | c.2616G>A (p.Gln872=) c.2580G>A (p.Gln860=) n.299G>A c.2694G>A (p.Gln898=) c.2658G>A (p.Gln886=) | |
19 | g.7141744T>A | CA403661793 | INSR | c.2615A>T (p.Gln872Leu) c.2579A>T (p.Gln860Leu) n.298A>T c.2693A>T (p.Gln898Leu) c.2657A>T (p.Gln886Leu) | |
19 | g.7141744T>C | CA403661792 | INSR | c.2615A>G (p.Gln872Arg) c.2579A>G (p.Gln860Arg) n.298A>G c.2693A>G (p.Gln898Arg) c.2657A>G (p.Gln886Arg) | |
19 | g.7141744T>G | CA403661790 | INSR | c.2615A>C (p.Gln872Pro) c.2579A>C (p.Gln860Pro) n.298A>C c.2693A>C (p.Gln898Pro) c.2657A>C (p.Gln886Pro) | dbSNP |
19 | g.7141744T= | CA2320775569 | INSR | c.2615A= (p.Gln872=) c.2579A= (p.Gln860=) n.298A= c.2693A= (p.Gln898=) c.2657A= (p.Gln886=) | |
19 | g.7141745G>A | CA403661796 | INSR | c.2614C>T (p.Gln872Ter) c.2578C>T (p.Gln860Ter) n.297C>T c.2692C>T (p.Gln898Ter) c.2656C>T (p.Gln886Ter) | |
19 | g.7141745G>C | CA403661798 | INSR | c.2614C>G (p.Gln872Glu) c.2578C>G (p.Gln860Glu) n.297C>G c.2692C>G (p.Gln898Glu) c.2656C>G (p.Gln886Glu) | |
19 | g.7141745G>T | CA403661799 | INSR | c.2614C>A (p.Gln872Lys) c.2578C>A (p.Gln860Lys) n.297C>A c.2692C>A (p.Gln898Lys) c.2656C>A (p.Gln886Lys) | |
19 | g.7141746C>A | CA403661802 | INSR | c.2613G>T (p.Trp871Cys) c.2577G>T (p.Trp859Cys) n.296G>T c.2691G>T (p.Trp897Cys) c.2655G>T (p.Trp885Cys) | |
19 | g.7141746C>G | CA403661804 | INSR | c.2613G>C (p.Trp871Cys) c.2577G>C (p.Trp859Cys) n.296G>C c.2691G>C (p.Trp897Cys) c.2655G>C (p.Trp885Cys) | |
19 | g.7141746C>T | CA403661805 | INSR | c.2613G>A (p.Trp871Ter) c.2577G>A (p.Trp859Ter) n.296G>A c.2691G>A (p.Trp897Ter) c.2655G>A (p.Trp885Ter) | |
19 | g.7141747C>A | CA403661808 | INSR | c.2612G>T (p.Trp871Leu) c.2576G>T (p.Trp859Leu) n.295G>T c.2690G>T (p.Trp897Leu) c.2654G>T (p.Trp885Leu) | |
19 | g.7141747C>G | CA403661810 | INSR | c.2612G>C (p.Trp871Ser) c.2576G>C (p.Trp859Ser) n.295G>C c.2690G>C (p.Trp897Ser) c.2654G>C (p.Trp885Ser) | |
19 | g.7141747C>T | CA403661811 | INSR | c.2612G>A (p.Trp871Ter) c.2576G>A (p.Trp859Ter) n.295G>A c.2690G>A (p.Trp897Ter) c.2654G>A (p.Trp885Ter) | |
19 | g.7141748A>C | CA403661813 | INSR | c.2611T>G (p.Trp871Gly) c.2575T>G (p.Trp859Gly) n.294T>G c.2689T>G (p.Trp897Gly) c.2653T>G (p.Trp885Gly) | |
19 | g.7141748A>G | CA403661815 | INSR | c.2611T>C (p.Trp871Arg) c.2575T>C (p.Trp859Arg) n.294T>C c.2689T>C (p.Trp897Arg) c.2653T>C (p.Trp885Arg) | |
19 | g.7141748A>T | CA403661817 | INSR | c.2611T>A (p.Trp871Arg) c.2575T>A (p.Trp859Arg) n.294T>A c.2689T>A (p.Trp897Arg) c.2653T>A (p.Trp885Arg) | |
19 | g.7141749C>A | CA403661821 | INSR | c.2610G>T (p.Met870Ile) c.2574G>T (p.Met858Ile) n.293G>T c.2688G>T (p.Met896Ile) c.2652G>T (p.Met884Ile) | |
19 | g.7141749C>G | CA403661823 | INSR | c.2610G>C (p.Met870Ile) c.2574G>C (p.Met858Ile) n.293G>C c.2688G>C (p.Met896Ile) c.2652G>C (p.Met884Ile) | |
19 | g.7141749C>T | CA403661820 | INSR | c.2610G>A (p.Met870Ile) c.2574G>A (p.Met858Ile) n.293G>A c.2688G>A (p.Met896Ile) c.2652G>A (p.Met884Ile) | |
19 | g.7141750A>C | CA403661826 | INSR | c.2609T>G (p.Met870Arg) c.2573T>G (p.Met858Arg) n.292T>G c.2687T>G (p.Met896Arg) c.2651T>G (p.Met884Arg) | |
19 | g.7141750A>G | CA403661827 | INSR | c.2609T>C (p.Met870Thr) c.2573T>C (p.Met858Thr) n.292T>C c.2687T>C (p.Met896Thr) c.2651T>C (p.Met884Thr) | |
19 | g.7141750A>T | CA403661829 | INSR | c.2609T>A (p.Met870Lys) c.2573T>A (p.Met858Lys) n.292T>A c.2687T>A (p.Met896Lys) c.2651T>A (p.Met884Lys) | |
19 | g.7141751T>A | CA403661832 | INSR | c.2608A>T (p.Met870Leu) c.2572A>T (p.Met858Leu) n.291A>T c.2686A>T (p.Met896Leu) c.2650A>T (p.Met884Leu) | |
19 | g.7141751T>C | CA403661834 | INSR | c.2608A>G (p.Met870Val) c.2572A>G (p.Met858Val) n.291A>G c.2686A>G (p.Met896Val) c.2650A>G (p.Met884Val) | COSMIC COSMIC |
19 | g.7141751T>G | CA403661836 | INSR | c.2608A>C (p.Met870Leu) c.2572A>C (p.Met858Leu) n.291A>C c.2686A>C (p.Met896Leu) c.2650A>C (p.Met884Leu) | |
19 | g.7141752C>A | CA403661837 | INSR | c.2607G>T (p.Leu869Phe) c.2571G>T (p.Leu857Phe) n.290G>T c.2685G>T (p.Leu895Phe) c.2649G>T (p.Leu883Phe) | |
19 | g.7141752C>G | CA403661839 | INSR | c.2607G>C (p.Leu869Phe) c.2571G>C (p.Leu857Phe) n.290G>C c.2685G>C (p.Leu895Phe) c.2649G>C (p.Leu883Phe) | |
19 | g.7141752C>T | CA505193504 | INSR | c.2607G>A (p.Leu869=) c.2571G>A (p.Leu857=) n.290G>A c.2685G>A (p.Leu895=) c.2649G>A (p.Leu883=) | |
19 | g.7141753A>C | CA403661842 | INSR | c.2606T>G (p.Leu869Trp) c.2570T>G (p.Leu857Trp) n.289T>G c.2684T>G (p.Leu895Trp) c.2648T>G (p.Leu883Trp) | |
19 | g.7141753A>G | CA403661843 | INSR | c.2606T>C (p.Leu869Ser) c.2570T>C (p.Leu857Ser) n.289T>C c.2684T>C (p.Leu895Ser) c.2648T>C (p.Leu883Ser) | |
19 | g.7141753A>T | CA403661845 | INSR | c.2606T>A (p.Leu869Ter) c.2570T>A (p.Leu857Ter) n.289T>A c.2684T>A (p.Leu895Ter) c.2648T>A (p.Leu883Ter) | |
19 | g.7141754A= | CA2320775570 | INSR | c.2605T= (p.Leu869=) c.2569T= (p.Leu857=) n.288T= c.2683T= (p.Leu895=) c.2647T= (p.Leu883=) | |
19 | g.7141754A>C | CA9135501 | INSR | c.2605T>G (p.Leu869Val) c.2569T>G (p.Leu857Val) n.288T>G c.2683T>G (p.Leu895Val) c.2647T>G (p.Leu883Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.7141754A>G | CA505193505 | INSR | c.2605T>C (p.Leu869=) c.2569T>C (p.Leu857=) n.288T>C c.2683T>C (p.Leu895=) c.2647T>C (p.Leu883=) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.7141754A>T | CA403661848 | INSR | c.2605T>A (p.Leu869Met) c.2569T>A (p.Leu857Met) n.288T>A c.2683T>A (p.Leu895Met) c.2647T>A (p.Leu883Met) | |
19 | g.7141755G>A | CA505193506 | INSR | c.2604C>T (p.His868=) c.2568C>T (p.His856=) n.287C>T c.2682C>T (p.His894=) c.2646C>T (p.His882=) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.7141755G>C | CA403661851 | INSR | c.2604C>G (p.His868Gln) c.2568C>G (p.His856Gln) n.287C>G c.2682C>G (p.His894Gln) c.2646C>G (p.His882Gln) | |
19 | g.7141755G= | CA2320775571 | INSR | c.2604C= (p.His868=) c.2568C= (p.His856=) n.287C= c.2682C= (p.His894=) c.2646C= (p.His882=) | |
19 | g.7141755G>T | CA403661850 | INSR | c.2604C>A (p.His868Gln) c.2568C>A (p.His856Gln) n.287C>A c.2682C>A (p.His894Gln) c.2646C>A (p.His882Gln) | |
19 | g.7141756T>A | CA403661853 | INSR | c.2603A>T (p.His868Leu) c.2567A>T (p.His856Leu) n.286A>T c.2681A>T (p.His894Leu) c.2645A>T (p.His882Leu) | |
19 | g.7141756T>C | CA403661854 | INSR | c.2603A>G (p.His868Arg) c.2567A>G (p.His856Arg) n.286A>G c.2681A>G (p.His894Arg) c.2645A>G (p.His882Arg) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7141756T>G | CA403661856 | INSR | c.2603A>C (p.His868Pro) c.2567A>C (p.His856Pro) n.286A>C c.2681A>C (p.His894Pro) c.2645A>C (p.His882Pro) | |
19 | g.7141756T= | CA2320775572 | INSR | c.2603A= (p.His868=) c.2567A= (p.His856=) n.286A= c.2681A= (p.His894=) c.2645A= (p.His882=) | |
19 | g.7141757G>A | CA9135502 | INSR | c.2602C>T (p.His868Tyr) c.2566C>T (p.His856Tyr) n.285C>T c.2680C>T (p.His894Tyr) c.2644C>T (p.His882Tyr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.7141757G>C | CA403661859 | INSR | c.2602C>G (p.His868Asp) c.2566C>G (p.His856Asp) n.285C>G c.2680C>G (p.His894Asp) c.2644C>G (p.His882Asp) | |
19 | g.7141757G= | CA2320775573 | INSR | c.2602C= (p.His868=) c.2566C= (p.His856=) n.285C= c.2680C= (p.His894=) c.2644C= (p.His882=) | |
19 | g.7141757G>T | CA403661861 | INSR | c.2602C>A (p.His868Asn) c.2566C>A (p.His856Asn) n.285C>A c.2680C>A (p.His894Asn) c.2644C>A (p.His882Asn) | |
19 | g.7141758G>A | CA505193507 | INSR | c.2601C>T (p.Val867=) c.2565C>T (p.Val855=) n.284C>T c.2679C>T (p.Val893=) c.2643C>T (p.Val881=) | |
19 | g.7141758G>C | CA505193509 | INSR | c.2601C>G (p.Val867=) c.2565C>G (p.Val855=) n.284C>G c.2679C>G (p.Val893=) c.2643C>G (p.Val881=) | |
19 | g.7141758G>T | CA505193508 | INSR | c.2601C>A (p.Val867=) c.2565C>A (p.Val855=) n.284C>A c.2679C>A (p.Val893=) c.2643C>A (p.Val881=) | |
19 | g.7141759A>C | CA403661864 | INSR | c.2600T>G (p.Val867Gly) c.2564T>G (p.Val855Gly) n.283T>G c.2678T>G (p.Val893Gly) c.2642T>G (p.Val881Gly) | |
19 | g.7141759A>G | CA403661865 | INSR | c.2600T>C (p.Val867Ala) c.2564T>C (p.Val855Ala) n.283T>C c.2678T>C (p.Val893Ala) c.2642T>C (p.Val881Ala) | gnomAD v4 |
19 | g.7141759A>T | CA403661867 | INSR | c.2600T>A (p.Val867Asp) c.2564T>A (p.Val855Asp) n.283T>A c.2678T>A (p.Val893Asp) c.2642T>A (p.Val881Asp) | |
19 | g.7141760C>A | CA403661869 | INSR | c.2599G>T (p.Val867Phe) c.2563G>T (p.Val855Phe) n.282G>T c.2677G>T (p.Val893Phe) c.2641G>T (p.Val881Phe) | |
19 | g.7141760C= | CA2320775574 | INSR | c.2599G= (p.Val867=) c.2563G= (p.Val855=) n.282G= c.2677G= (p.Val893=) c.2641G= (p.Val881=) | |
19 | g.7141760C>G | CA403661871 | INSR | c.2599G>C (p.Val867Leu) c.2563G>C (p.Val855Leu) n.282G>C c.2677G>C (p.Val893Leu) c.2641G>C (p.Val881Leu) | |
19 | g.7141760C>T | CA9135503 | INSR | c.2599G>A (p.Val867Ile) c.2563G>A (p.Val855Ile) n.282G>A c.2677G>A (p.Val893Ile) c.2641G>A (p.Val881Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7141761G>A | CA205421 | INSR | c.2598C>T (p.Val866=) c.2562C>T (p.Val854=) n.281C>T c.2676C>T (p.Val892=) c.2640C>T (p.Val880=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7141761G>C | CA505193510 | INSR | c.2598C>G (p.Val866=) c.2562C>G (p.Val854=) n.281C>G c.2676C>G (p.Val892=) c.2640C>G (p.Val880=) | |
19 | g.7141761G= | CA2320775575 | INSR | c.2598C= (p.Val866=) c.2562C= (p.Val854=) n.281C= c.2676C= (p.Val892=) c.2640C= (p.Val880=) | |
19 | g.7141761G>T | CA505193511 | INSR | c.2598C>A (p.Val866=) c.2562C>A (p.Val854=) n.281C>A c.2676C>A (p.Val892=) c.2640C>A (p.Val880=) | |
19 | g.7141762A>C | CA403661877 | INSR | c.2597T>G (p.Val866Gly) c.2561T>G (p.Val854Gly) n.280T>G c.2675T>G (p.Val892Gly) c.2639T>G (p.Val880Gly) | |
19 | g.7141762A>G | CA403661876 | INSR | c.2597T>C (p.Val866Ala) c.2561T>C (p.Val854Ala) n.280T>C c.2675T>C (p.Val892Ala) c.2639T>C (p.Val880Ala) | |
19 | g.7141762A>T | CA403661875 | INSR | c.2597T>A (p.Val866Asp) c.2561T>A (p.Val854Asp) n.280T>A c.2675T>A (p.Val892Asp) c.2639T>A (p.Val880Asp) | |
19 | g.7141763C>A | CA403661879 | INSR | c.2596G>T (p.Val866Phe) c.2560G>T (p.Val854Phe) n.279G>T c.2674G>T (p.Val892Phe) c.2638G>T (p.Val880Phe) | |
19 | g.7141763C= | CA2320775576 | INSR | c.2596G= (p.Val866=) c.2560G= (p.Val854=) n.279G= c.2674G= (p.Val892=) c.2638G= (p.Val880=) | |
19 | g.7141763C>G | CA403661881 | INSR | c.2596G>C (p.Val866Leu) c.2560G>C (p.Val854Leu) n.279G>C c.2674G>C (p.Val892Leu) c.2638G>C (p.Val880Leu) | |
19 | g.7141763C>T | CA9135504 | INSR | c.2596G>A (p.Val866Ile) c.2560G>A (p.Val854Ile) n.279G>A c.2674G>A (p.Val892Ile) c.2638G>A (p.Val880Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7141763_7141766delinsCGTT | CA2320775577 | INSR | c.2593_2596delinsAACG (p.Asn865=) c.2557_2560delinsAACG (p.Asn853=) n.276_279delinsAACG c.2671_2674delinsAACG (p.Asn891=) c.2635_2638delinsAACG (p.Asn879=) | |
19 | g.7141764G>A | CA9135505 | INSR | c.2595C>T (p.Asn865=) c.2559C>T (p.Asn853=) n.278C>T c.2673C>T (p.Asn891=) c.2637C>T (p.Asn879=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7141764G>C | CA403661884 | INSR | c.2595C>G (p.Asn865Lys) c.2559C>G (p.Asn853Lys) n.278C>G c.2673C>G (p.Asn891Lys) c.2637C>G (p.Asn879Lys) | |
19 | g.7141764G= | CA2320775579 | INSR | c.2595C= (p.Asn865=) c.2559C= (p.Asn853=) n.278C= c.2673C= (p.Asn891=) c.2637C= (p.Asn879=) | |
19 | g.7141764G>T | CA403661886 | INSR | c.2595C>A (p.Asn865Lys) c.2559C>A (p.Asn853Lys) n.278C>A c.2673C>A (p.Asn891Lys) c.2637C>A (p.Asn879Lys) | |
19 | g.7141767_7141769del | CA2320775578 | INSR | c.2593_2595del (p.Asn865del) c.2557_2559del (p.Asn853del) n.276_278del c.2671_2673del (p.Asn891del) c.2635_2637del (p.Asn879del) | dbSNP |
19 | g.7141765T>A | CA403661888 | INSR | c.2594A>T (p.Asn865Ile) c.2558A>T (p.Asn853Ile) n.277A>T c.2672A>T (p.Asn891Ile) c.2636A>T (p.Asn879Ile) | |
19 | g.7141765T>C | CA403661890 | INSR | c.2594A>G (p.Asn865Ser) c.2558A>G (p.Asn853Ser) n.277A>G c.2672A>G (p.Asn891Ser) c.2636A>G (p.Asn879Ser) | gnomAD v4 |
19 | g.7141765T>G | CA403661892 | INSR | c.2594A>C (p.Asn865Thr) c.2558A>C (p.Asn853Thr) n.277A>C c.2672A>C (p.Asn891Thr) c.2636A>C (p.Asn879Thr) | |
19 | g.7141766del | CA2587922996 | INSR | c.2594del (p.Asn865ThrfsTer5) c.2558del (p.Asn853ThrfsTer5) n.277del c.2672del (p.Asn891ThrfsTer5) c.2636del (p.Asn879ThrfsTer5) | gnomAD v4 |
19 | g.7141766T>A | CA403661900 | INSR | c.2593A>T (p.Asn865Tyr) c.2557A>T (p.Asn853Tyr) n.276A>T c.2671A>T (p.Asn891Tyr) c.2635A>T (p.Asn879Tyr) | gnomAD v4 |
19 | g.7141766T>C | CA403661899 | INSR | c.2593A>G (p.Asn865Asp) c.2557A>G (p.Asn853Asp) n.276A>G c.2671A>G (p.Asn891Asp) c.2635A>G (p.Asn879Asp) | |
19 | g.7141766T>G | CA403661896 | INSR | c.2593A>C (p.Asn865His) c.2557A>C (p.Asn853His) n.276A>C c.2671A>C (p.Asn891His) c.2635A>C (p.Asn879His) | |
19 | g.7141767G>A | CA9135506 | INSR | c.2592C>T (p.Asn864=) c.2556C>T (p.Asn852=) n.275C>T c.2670C>T (p.Asn890=) c.2634C>T (p.Asn878=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.7141767G>C | CA403661904 | INSR | c.2592C>G (p.Asn864Lys) c.2556C>G (p.Asn852Lys) n.275C>G c.2670C>G (p.Asn890Lys) c.2634C>G (p.Asn878Lys) | |
19 | g.7141767G= | CA2320775580 | INSR | c.2592C= (p.Asn864=) c.2556C= (p.Asn852=) n.275C= c.2670C= (p.Asn890=) c.2634C= (p.Asn878=) | |
19 | g.7141767G>T | CA403661906 | INSR | c.2592C>A (p.Asn864Lys) c.2556C>A (p.Asn852Lys) n.275C>A c.2670C>A (p.Asn890Lys) c.2634C>A (p.Asn878Lys) | gnomAD v4 |
19 | g.7141767_7141768delinsGT | CA2320775581 | INSR | c.2591_2592delinsAC (p.Asn864=) c.2555_2556delinsAC (p.Asn852=) n.274_275delinsAC c.2669_2670delinsAC (p.Asn890=) c.2633_2634delinsAC (p.Asn878=) | |
19 | g.7141768T>A | CA403661909 | INSR | c.2591A>T (p.Asn864Ile) c.2555A>T (p.Asn852Ile) n.274A>T c.2669A>T (p.Asn890Ile) c.2633A>T (p.Asn878Ile) | |
19 | g.7141768T>C | CA9135507 | INSR | c.2591A>G (p.Asn864Ser) c.2555A>G (p.Asn852Ser) n.274A>G c.2669A>G (p.Asn890Ser) c.2633A>G (p.Asn878Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7141768T>G | CA403661911 | INSR | c.2591A>C (p.Asn864Thr) c.2555A>C (p.Asn852Thr) n.274A>C c.2669A>C (p.Asn890Thr) c.2633A>C (p.Asn878Thr) | |
19 | g.7141768T= | CA2320775582 | INSR | c.2591A= (p.Asn864=) c.2555A= (p.Asn852=) n.274A= c.2669A= (p.Asn890=) c.2633A= (p.Asn878=) | |
19 | g.7141769del | CA631680233 | INSR | c.2591del (p.Asn864ThrfsTer6) c.2555del (p.Asn852ThrfsTer6) n.274del c.2669del (p.Asn890ThrfsTer6) c.2633del (p.Asn878ThrfsTer6) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.7141769T>A | CA403661916 | INSR | c.2590A>T (p.Asn864Tyr) c.2554A>T (p.Asn852Tyr) n.273A>T c.2668A>T (p.Asn890Tyr) c.2632A>T (p.Asn878Tyr) | |
19 | g.7141769T>C | CA403661913 | INSR | c.2590A>G (p.Asn864Asp) c.2554A>G (p.Asn852Asp) n.273A>G c.2668A>G (p.Asn890Asp) c.2632A>G (p.Asn878Asp) | |
19 | g.7141769T>G | CA403661915 | INSR | c.2590A>C (p.Asn864His) c.2554A>C (p.Asn852His) n.273A>C c.2668A>C (p.Asn890His) c.2632A>C (p.Asn878His) | |
19 | g.7141770C>A | CA403661918 | INSR | c.2589G>T (p.Glu863Asp) c.2553G>T (p.Glu851Asp) n.272G>T c.2667G>T (p.Glu889Asp) c.2631G>T (p.Glu877Asp) | |
19 | g.7141770C= | CA2320775583 | INSR | c.2589G= (p.Glu863=) c.2553G= (p.Glu851=) n.272G= c.2667G= (p.Glu889=) c.2631G= (p.Glu877=) | |
19 | g.7141770C>G | CA403661919 | INSR | c.2589G>C (p.Glu863Asp) c.2553G>C (p.Glu851Asp) n.272G>C c.2667G>C (p.Glu889Asp) c.2631G>C (p.Glu877Asp) | |
19 | g.7141770C>T | CA505193512 | INSR | c.2589G>A (p.Glu863=) c.2553G>A (p.Glu851=) n.272G>A c.2667G>A (p.Glu889=) c.2631G>A (p.Glu877=) | dbSNP |
19 | g.7141771T>A | CA403661922 | INSR | c.2588A>T (p.Glu863Val) c.2552A>T (p.Glu851Val) n.271A>T c.2666A>T (p.Glu889Val) c.2630A>T (p.Glu877Val) | |
19 | g.7141771T>C | CA403661924 | INSR | c.2588A>G (p.Glu863Gly) c.2552A>G (p.Glu851Gly) n.271A>G c.2666A>G (p.Glu889Gly) c.2630A>G (p.Glu877Gly) | |
19 | g.7141771T>G | CA403661925 | INSR | c.2588A>C (p.Glu863Ala) c.2552A>C (p.Glu851Ala) n.271A>C c.2666A>C (p.Glu889Ala) c.2630A>C (p.Glu877Ala) | |
19 | g.7141772C>A | CA403661928 | INSR | c.2587G>T (p.Glu863Ter) c.2551G>T (p.Glu851Ter) n.270G>T c.2665G>T (p.Glu889Ter) c.2629G>T (p.Glu877Ter) | |
19 | g.7141772C>G | CA403661930 | INSR | c.2587G>C (p.Glu863Gln) c.2551G>C (p.Glu851Gln) n.270G>C c.2665G>C (p.Glu889Gln) c.2629G>C (p.Glu877Gln) | |
19 | g.7141772C>T | CA403661931 | INSR | c.2587G>A (p.Glu863Lys) c.2551G>A (p.Glu851Lys) n.270G>A c.2665G>A (p.Glu889Lys) c.2629G>A (p.Glu877Lys) | COSMIC COSMIC |
19 | g.7141773A>C | CA403661934 | INSR | c.2586T>G (p.Phe862Leu) c.2550T>G (p.Phe850Leu) n.269T>G c.2664T>G (p.Phe888Leu) c.2628T>G (p.Phe876Leu) | |
19 | g.7141773A>G | CA505193513 | INSR | c.2586T>C (p.Phe862=) c.2550T>C (p.Phe850=) n.269T>C c.2664T>C (p.Phe888=) c.2628T>C (p.Phe876=) | |
19 | g.7141773A>T | CA403661935 | INSR | c.2586T>A (p.Phe862Leu) c.2550T>A (p.Phe850Leu) n.269T>A c.2664T>A (p.Phe888Leu) c.2628T>A (p.Phe876Leu) | |
19 | g.7141775del | CA2587922997 | INSR | c.2586del (p.Phe862LeufsTer8) c.2550del (p.Phe850LeufsTer8) n.269del c.2664del (p.Phe888LeufsTer8) c.2628del (p.Phe876LeufsTer8) | gnomAD v4 |
19 | g.7141774A>C | CA403661937 | INSR | c.2585T>G (p.Phe862Cys) c.2549T>G (p.Phe850Cys) n.268T>G c.2663T>G (p.Phe888Cys) c.2627T>G (p.Phe876Cys) | |
19 | g.7141774A>G | CA403661939 | INSR | c.2585T>C (p.Phe862Ser) c.2549T>C (p.Phe850Ser) n.268T>C c.2663T>C (p.Phe888Ser) c.2627T>C (p.Phe876Ser) | COSMIC COSMIC |
19 | g.7141774A>T | CA403661941 | INSR | c.2585T>A (p.Phe862Tyr) c.2549T>A (p.Phe850Tyr) n.268T>A c.2663T>A (p.Phe888Tyr) c.2627T>A (p.Phe876Tyr) | |
19 | g.7141775A>C | CA403661943 | INSR | c.2584T>G (p.Phe862Val) c.2548T>G (p.Phe850Val) n.267T>G c.2662T>G (p.Phe888Val) c.2626T>G (p.Phe876Val) | |
19 | g.7141775A>G | CA403661947 | INSR | c.2584T>C (p.Phe862Leu) c.2548T>C (p.Phe850Leu) n.267T>C c.2662T>C (p.Phe888Leu) c.2626T>C (p.Phe876Leu) | dbSNP |
19 | g.7141775A>T | CA403661945 | INSR | c.2584T>A (p.Phe862Ile) c.2548T>A (p.Phe850Ile) n.267T>A c.2662T>A (p.Phe888Ile) c.2626T>A (p.Phe876Ile) | |
19 | g.7141776G>A | CA505193514 | INSR | c.2583C>T (p.Ile861=) c.2547C>T (p.Ile849=) n.266C>T c.2661C>T (p.Ile887=) c.2625C>T (p.Ile875=) | |
19 | g.7141776G>C | CA403661949 | INSR | c.2583C>G (p.Ile861Met) c.2547C>G (p.Ile849Met) n.266C>G c.2661C>G (p.Ile887Met) c.2625C>G (p.Ile875Met) | |
19 | g.7141776G>T | CA505193515 | INSR | c.2583C>A (p.Ile861=) c.2547C>A (p.Ile849=) n.266C>A c.2661C>A (p.Ile887=) c.2625C>A (p.Ile875=) | |
19 | g.7141777A= | CA2320775584 | INSR | c.2582T= (p.Ile861=) c.2546T= (p.Ile849=) n.265T= c.2660T= (p.Ile887=) c.2624T= (p.Ile875=) | |
19 | g.7141777A>C | CA403661951 | INSR | c.2582T>G (p.Ile861Ser) c.2546T>G (p.Ile849Ser) n.265T>G c.2660T>G (p.Ile887Ser) c.2624T>G (p.Ile875Ser) | |
19 | g.7141777A>G | CA9135508 | INSR | c.2582T>C (p.Ile861Thr) c.2546T>C (p.Ile849Thr) n.265T>C c.2660T>C (p.Ile887Thr) c.2624T>C (p.Ile875Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7141777A>T | CA403661954 | INSR | c.2582T>A (p.Ile861Asn) c.2546T>A (p.Ile849Asn) n.265T>A c.2660T>A (p.Ile887Asn) c.2624T>A (p.Ile875Asn) | |
19 | g.7141778T>A | CA403661957 | INSR | c.2581A>T (p.Ile861Phe) c.2545A>T (p.Ile849Phe) n.264A>T c.2659A>T (p.Ile887Phe) c.2623A>T (p.Ile875Phe) | |
19 | g.7141778T>C | CA403661959 | INSR | c.2581A>G (p.Ile861Val) c.2545A>G (p.Ile849Val) n.264A>G c.2659A>G (p.Ile887Val) c.2623A>G (p.Ile875Val) | dbSNP gnomAD v4 |
19 | g.7141778T>G | CA403661960 | INSR | c.2581A>C (p.Ile861Leu) c.2545A>C (p.Ile849Leu) n.264A>C c.2659A>C (p.Ile887Leu) c.2623A>C (p.Ile875Leu) | gnomAD v4 |
19 | g.7141778T= | CA2320775585 | INSR | c.2581A= (p.Ile861=) c.2545A= (p.Ile849=) n.264A= c.2659A= (p.Ile887=) c.2623A= (p.Ile875=) | |
19 | g.7141779T>A | CA403661961 | INSR | c.2580A>T (p.Glu860Asp) c.2544A>T (p.Glu848Asp) n.263A>T c.2658A>T (p.Glu886Asp) c.2622A>T (p.Glu874Asp) | |
19 | g.7141779T>C | CA505193516 | INSR | c.2580A>G (p.Glu860=) c.2544A>G (p.Glu848=) n.263A>G c.2658A>G (p.Glu886=) c.2622A>G (p.Glu874=) | |
19 | g.7141779T>G | CA403661963 | INSR | c.2580A>C (p.Glu860Asp) c.2544A>C (p.Glu848Asp) n.263A>C c.2658A>C (p.Glu886Asp) c.2622A>C (p.Glu874Asp) | |
19 | g.7141780T>A | CA403661966 | INSR | c.2579A>T (p.Glu860Val) c.2543A>T (p.Glu848Val) n.262A>T c.2657A>T (p.Glu886Val) c.2621A>T (p.Glu874Val) | |
19 | g.7141780T>C | CA403661967 | INSR | c.2579A>G (p.Glu860Gly) c.2543A>G (p.Glu848Gly) n.262A>G c.2657A>G (p.Glu886Gly) c.2621A>G (p.Glu874Gly) | |
19 | g.7141780T>G | CA403661970 | INSR | c.2579A>C (p.Glu860Ala) c.2543A>C (p.Glu848Ala) n.262A>C c.2657A>C (p.Glu886Ala) c.2621A>C (p.Glu874Ala) | |
19 | g.7141781C>A | CA403661976 | INSR | c.2578G>T (p.Glu860Ter) c.2542G>T (p.Glu848Ter) n.261G>T c.2656G>T (p.Glu886Ter) c.2620G>T (p.Glu874Ter) | |
19 | g.7141781C>G | CA403661974 | INSR | c.2578G>C (p.Glu860Gln) c.2542G>C (p.Glu848Gln) n.261G>C c.2656G>C (p.Glu886Gln) c.2620G>C (p.Glu874Gln) | |
19 | g.7141781C>T | CA403661972 | INSR | c.2578G>A (p.Glu860Lys) c.2542G>A (p.Glu848Lys) n.261G>A c.2656G>A (p.Glu886Lys) c.2620G>A (p.Glu874Lys) | |
19 | g.7141782A>C | CA403661978 | INSR | c.2577T>G (p.His859Gln) c.2541T>G (p.His847Gln) n.260T>G c.2655T>G (p.His885Gln) c.2619T>G (p.His873Gln) | |
19 | g.7141782A>G | CA505193517 | INSR | c.2577T>C (p.His859=) c.2541T>C (p.His847=) n.260T>C c.2655T>C (p.His885=) c.2619T>C (p.His873=) | |
19 | g.7141782A>T | CA403661979 | INSR | c.2577T>A (p.His859Gln) c.2541T>A (p.His847Gln) n.260T>A c.2655T>A (p.His885Gln) c.2619T>A (p.His873Gln) | |
19 | g.7141783T>A | CA403661981 | INSR | c.2576A>T (p.His859Leu) c.2540A>T (p.His847Leu) n.259A>T c.2654A>T (p.His885Leu) c.2618A>T (p.His873Leu) | |
19 | g.7141783T>C | CA403661983 | INSR | c.2576A>G (p.His859Arg) c.2540A>G (p.His847Arg) n.259A>G c.2654A>G (p.His885Arg) c.2618A>G (p.His873Arg) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7141783T>G | CA403661985 | INSR | c.2576A>C (p.His859Pro) c.2540A>C (p.His847Pro) n.259A>C c.2654A>C (p.His885Pro) c.2618A>C (p.His873Pro) | |
19 | g.7141783T= | CA2320775586 | INSR | c.2576A= (p.His859=) c.2540A= (p.His847=) n.259A= c.2654A= (p.His885=) c.2618A= (p.His873=) | |
19 | g.7141784G>A | CA9135509 | INSR | c.2575C>T (p.His859Tyr) c.2539C>T (p.His847Tyr) n.258C>T c.2653C>T (p.His885Tyr) c.2617C>T (p.His873Tyr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7141784G>C | CA403661988 | INSR | c.2575C>G (p.His859Asp) c.2539C>G (p.His847Asp) n.258C>G c.2653C>G (p.His885Asp) c.2617C>G (p.His873Asp) | |
19 | g.7141784G= | CA2320775587 | INSR | c.2575C= (p.His859=) c.2539C= (p.His847=) n.258C= c.2653C= (p.His885=) c.2617C= (p.His873=) | |
19 | g.7141784G>T | CA403661990 | INSR | c.2575C>A (p.His859Asn) c.2539C>A (p.His847Asn) n.258C>A c.2653C>A (p.His885Asn) c.2617C>A (p.His873Asn) | |
19 | g.7141785C>A | CA505193518 | INSR | c.2574G>T (p.Thr858=) c.2538G>T (p.Thr846=) n.257G>T c.2652G>T (p.Thr884=) c.2616G>T (p.Thr872=) | gnomAD v4 |
19 | g.7141785C= | CA2320775588 | INSR | c.2574G= (p.Thr858=) c.2538G= (p.Thr846=) n.257G= c.2652G= (p.Thr884=) c.2616G= (p.Thr872=) | |
19 | g.7141785C>G | CA505193519 | INSR | c.2574G>C (p.Thr858=) c.2538G>C (p.Thr846=) n.257G>C c.2652G>C (p.Thr884=) c.2616G>C (p.Thr872=) | COSMIC COSMIC |
19 | g.7141785C>T | CA9135510 | INSR | c.2574G>A (p.Thr858=) c.2538G>A (p.Thr846=) n.257G>A c.2652G>A (p.Thr884=) c.2616G>A (p.Thr872=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7141786G>A | CA9135511 | INSR | c.2573C>T (p.Thr858Met) c.2537C>T (p.Thr846Met) n.256C>T c.2651C>T (p.Thr884Met) c.2615C>T (p.Thr872Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7141786G>C | CA403661995 | INSR | c.2573C>G (p.Thr858Arg) c.2537C>G (p.Thr846Arg) n.256C>G c.2651C>G (p.Thr884Arg) c.2615C>G (p.Thr872Arg) | gnomAD v4 |
19 | g.7141786G= | CA2320775589 | INSR | c.2573C= (p.Thr858=) c.2537C= (p.Thr846=) n.256C= c.2651C= (p.Thr884=) c.2615C= (p.Thr872=) | |
19 | g.7141786G>T | CA403661997 | INSR | c.2573C>A (p.Thr858Lys) c.2537C>A (p.Thr846Lys) n.256C>A c.2651C>A (p.Thr884Lys) c.2615C>A (p.Thr872Lys) | |
19 | g.7141787T>A | CA403661998 | INSR | c.2572A>T (p.Thr858Ser) c.2536A>T (p.Thr846Ser) n.255A>T c.2650A>T (p.Thr884Ser) c.2614A>T (p.Thr872Ser) | |
19 | g.7141787T>C | CA9135512 | INSR | c.2572A>G (p.Thr858Ala) c.2536A>G (p.Thr846Ala) n.255A>G c.2650A>G (p.Thr884Ala) c.2614A>G (p.Thr872Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7141787T>G | CA403662000 | INSR | c.2572A>C (p.Thr858Pro) c.2536A>C (p.Thr846Pro) n.255A>C c.2650A>C (p.Thr884Pro) c.2614A>C (p.Thr872Pro) | |
19 | g.7141787T= | CA2320775590 | INSR | c.2572A= (p.Thr858=) c.2536A= (p.Thr846=) n.255A= c.2650A= (p.Thr884=) c.2614A= (p.Thr872=) | |
19 | g.7141788C>A | CA505193520 | INSR | c.2571G>T (p.Val857=) c.2535G>T (p.Val845=) n.254G>T c.2649G>T (p.Val883=) c.2613G>T (p.Val871=) | |
19 | g.7141788C>G | CA505193521 | INSR | c.2571G>C (p.Val857=) c.2535G>C (p.Val845=) n.254G>C c.2649G>C (p.Val883=) c.2613G>C (p.Val871=) | |
19 | g.7141788C>T | CA505193522 | INSR | c.2571G>A (p.Val857=) c.2535G>A (p.Val845=) n.254G>A c.2649G>A (p.Val883=) c.2613G>A (p.Val871=) | |
19 | g.7141789A>C | CA403662003 | INSR | c.2570T>G (p.Val857Gly) c.2534T>G (p.Val845Gly) n.253T>G c.2648T>G (p.Val883Gly) c.2612T>G (p.Val871Gly) | |
19 | g.7141789A>G | CA403662007 | INSR | c.2570T>C (p.Val857Ala) c.2534T>C (p.Val845Ala) n.253T>C c.2648T>C (p.Val883Ala) c.2612T>C (p.Val871Ala) | |
19 | g.7141789A>T | CA403662005 | INSR | c.2570T>A (p.Val857Glu) c.2534T>A (p.Val845Glu) n.253T>A c.2648T>A (p.Val883Glu) c.2612T>A (p.Val871Glu) | |
19 | g.7141790C>A | CA403662009 | INSR | c.2569G>T (p.Val857Leu) c.2533G>T (p.Val845Leu) n.252G>T c.2647G>T (p.Val883Leu) c.2611G>T (p.Val871Leu) | |
19 | g.7141790C= | CA2320775591 | INSR | c.2569G= (p.Val857=) c.2533G= (p.Val845=) n.252G= c.2647G= (p.Val883=) c.2611G= (p.Val871=) | |
19 | g.7141790C>G | CA403662011 | INSR | c.2569G>C (p.Val857Leu) c.2533G>C (p.Val845Leu) n.252G>C c.2647G>C (p.Val883Leu) c.2611G>C (p.Val871Leu) | |
19 | g.7141790C>T | CA9135513 | INSR | c.2569G>A (p.Val857Met) c.2533G>A (p.Val845Met) n.252G>A c.2647G>A (p.Val883Met) c.2611G>A (p.Val871Met) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.7141791A= | CA2320775592 | INSR | c.2568T= (p.Pro856=) c.2532T= (p.Pro844=) n.251T= c.2646T= (p.Pro882=) c.2610T= (p.Pro870=) | |
19 | g.7141791A>C | CA505193523 | INSR | c.2568T>G (p.Pro856=) c.2532T>G (p.Pro844=) n.251T>G c.2646T>G (p.Pro882=) c.2610T>G (p.Pro870=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7141791A>G | CA505193524 | INSR | c.2568T>C (p.Pro856=) c.2532T>C (p.Pro844=) n.251T>C c.2646T>C (p.Pro882=) c.2610T>C (p.Pro870=) | gnomAD v4 |
19 | g.7141791A>T | CA505193525 | INSR | c.2568T>A (p.Pro856=) c.2532T>A (p.Pro844=) n.251T>A c.2646T>A (p.Pro882=) c.2610T>A (p.Pro870=) | |
19 | g.7141792G>A | CA403662014 | INSR | c.2567C>T (p.Pro856Leu) c.2531C>T (p.Pro844Leu) n.250C>T c.2645C>T (p.Pro882Leu) c.2609C>T (p.Pro870Leu) | |
19 | g.7141792G>C | CA403662015 | INSR | c.2567C>G (p.Pro856Arg) c.2531C>G (p.Pro844Arg) n.250C>G c.2645C>G (p.Pro882Arg) c.2609C>G (p.Pro870Arg) | gnomAD v4 |
19 | g.7141792G>T | CA403662017 | INSR | c.2567C>A (p.Pro856His) c.2531C>A (p.Pro844His) n.250C>A c.2645C>A (p.Pro882His) c.2609C>A (p.Pro870His) | |
19 | g.7141793G>A | CA403662020 | INSR | c.2566C>T (p.Pro856Ser) c.2530C>T (p.Pro844Ser) n.249C>T c.2644C>T (p.Pro882Ser) c.2608C>T (p.Pro870Ser) | |
19 | g.7141793G>C | CA403662021 | INSR | c.2566C>G (p.Pro856Ala) c.2530C>G (p.Pro844Ala) n.249C>G c.2644C>G (p.Pro882Ala) c.2608C>G (p.Pro870Ala) | |
19 | g.7141793G>T | CA403662022 | INSR | c.2566C>A (p.Pro856Thr) c.2530C>A (p.Pro844Thr) n.249C>A c.2644C>A (p.Pro882Thr) c.2608C>A (p.Pro870Thr) | |
19 | g.7141794G>A | CA505193528 | INSR | c.2565C>T (p.Gly855=) c.2529C>T (p.Gly843=) n.248C>T c.2643C>T (p.Gly881=) c.2607C>T (p.Gly869=) | |
19 | g.7141794G>C | CA505193527 | INSR | c.2565C>G (p.Gly855=) c.2529C>G (p.Gly843=) n.248C>G c.2643C>G (p.Gly881=) c.2607C>G (p.Gly869=) | |
19 | g.7141794G>T | CA505193526 | INSR | c.2565C>A (p.Gly855=) c.2529C>A (p.Gly843=) n.248C>A c.2643C>A (p.Gly881=) c.2607C>A (p.Gly869=) | gnomAD v4 |
19 | g.7141795C>A | CA403662024 | INSR | c.2564G>T (p.Gly855Val) c.2528G>T (p.Gly843Val) n.247G>T c.2642G>T (p.Gly881Val) c.2606G>T (p.Gly869Val) | |
19 | g.7141795C= | CA2320775593 | INSR | c.2564G= (p.Gly855=) c.2528G= (p.Gly843=) n.247G= c.2642G= (p.Gly881=) c.2606G= (p.Gly869=) | |
19 | g.7141795C>G | CA403662026 | INSR | c.2564G>C (p.Gly855Ala) c.2528G>C (p.Gly843Ala) n.247G>C c.2642G>C (p.Gly881Ala) c.2606G>C (p.Gly869Ala) | |
19 | g.7141795C>T | CA9135514 | INSR | c.2564G>A (p.Gly855Asp) c.2528G>A (p.Gly843Asp) n.247G>A c.2642G>A (p.Gly881Asp) c.2606G>A (p.Gly869Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |