Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.7131595_7132840del | CA124243 | INSR | c.2683-522_2842+564del c.2647-522_2806+564del c.2761-522_2920+564del c.2725-522_2884+564del | |
19 | g.7131614_7132859del | CA124244 | INSR | c.2683-542_2842+544del c.2647-542_2806+544del c.2761-542_2920+544del c.2725-542_2884+544del | |
19 | g.7132127C>G | CA2576595101 | INSR | c.2842+31G>C (n.2842+31G>C) c.2806+31G>C (n.2806+31G>C) c.2920+31G>C (n.2920+31G>C) c.2884+31G>C (n.2884+31G>C) | |
19 | g.7132128C>A | CA631723694 | INSR | c.2842+30G>T (n.2842+30G>T) c.2806+30G>T (n.2806+30G>T) c.2920+30G>T (n.2920+30G>T) c.2884+30G>T (n.2884+30G>T) | dbSNP gnomAD v2 |
19 | g.7132128C= | CA2320771036 | INSR | c.2842+30G= (n.2842+30G=) c.2806+30G= (n.2806+30G=) c.2920+30G= (n.2920+30G=) c.2884+30G= (n.2884+30G=) | |
19 | g.7132129A>C | CA2587922721 | INSR | c.2842+29T>G (n.2842+29T>G) c.2806+29T>G (n.2806+29T>G) c.2920+29T>G (n.2920+29T>G) c.2884+29T>G (n.2884+29T>G) | gnomAD v4 |
19 | g.7132130G>T | CA2576595102 | INSR | c.2842+28C>A (n.2842+28C>A) c.2806+28C>A (n.2806+28C>A) c.2920+28C>A (n.2920+28C>A) c.2884+28C>A (n.2884+28C>A) | gnomAD v4 |
19 | g.7132131T>C | CA2735472788 | INSR | c.2842+27A>G (n.2842+27A>G) c.2806+27A>G (n.2806+27A>G) c.2920+27A>G (n.2920+27A>G) c.2884+27A>G (n.2884+27A>G) | dbSNP |
19 | g.7132132C>T | CA2587922722 | INSR | c.2842+26G>A (n.2842+26G>A) c.2806+26G>A (n.2806+26G>A) c.2920+26G>A (n.2920+26G>A) c.2884+26G>A (n.2884+26G>A) | gnomAD v4 |
19 | g.7132134G>A | CA304878316 | INSR | c.2842+24C>T (n.2842+24C>T) c.2806+24C>T (n.2806+24C>T) c.2920+24C>T (n.2920+24C>T) c.2884+24C>T (n.2884+24C>T) | dbSNP |
19 | g.7132134G>C | CA2587922723 | INSR | c.2842+24C>G (n.2842+24C>G) c.2806+24C>G (n.2806+24C>G) c.2920+24C>G (n.2920+24C>G) c.2884+24C>G (n.2884+24C>G) | gnomAD v4 |
19 | g.7132134G= | CA2320771037 | INSR | c.2842+24C= (n.2842+24C=) c.2806+24C= (n.2806+24C=) c.2920+24C= (n.2920+24C=) c.2884+24C= (n.2884+24C=) | |
19 | g.7132136T>C | CA2587922724 | INSR | c.2842+22A>G (n.2842+22A>G) c.2806+22A>G (n.2806+22A>G) c.2920+22A>G (n.2920+22A>G) c.2884+22A>G (n.2884+22A>G) | gnomAD v4 |
19 | g.7132136T>G | CA2576595103 | INSR | c.2842+22A>C (n.2842+22A>C) c.2806+22A>C (n.2806+22A>C) c.2920+22A>C (n.2920+22A>C) c.2884+22A>C (n.2884+22A>C) | gnomAD v4 |
19 | g.7132137G>A | CA631723695 | INSR | c.2842+21C>T (n.2842+21C>T) c.2806+21C>T (n.2806+21C>T) c.2920+21C>T (n.2920+21C>T) c.2884+21C>T (n.2884+21C>T) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.7132137G= | CA2320771038 | INSR | c.2842+21C= (n.2842+21C=) c.2806+21C= (n.2806+21C=) c.2920+21C= (n.2920+21C=) c.2884+21C= (n.2884+21C=) | |
19 | g.7132138A>G | CA2576595104 | INSR | c.2842+20T>C (n.2842+20T>C) c.2806+20T>C (n.2806+20T>C) c.2920+20T>C (n.2920+20T>C) c.2884+20T>C (n.2884+20T>C) | |
19 | g.7132139G>C | CA9135442 | INSR | c.2842+19C>G (n.2842+19C>G) c.2806+19C>G (n.2806+19C>G) c.2920+19C>G (n.2920+19C>G) c.2884+19C>G (n.2884+19C>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.7132139G= | CA2320771039 | INSR | c.2842+19C= (n.2842+19C=) c.2806+19C= (n.2806+19C=) c.2920+19C= (n.2920+19C=) c.2884+19C= (n.2884+19C=) | |
19 | g.7132141C= | CA2320771040 | INSR | c.2842+17G= (n.2842+17G=) c.2806+17G= (n.2806+17G=) c.2920+17G= (n.2920+17G=) c.2884+17G= (n.2884+17G=) | |
19 | g.7132141C>G | CA2587922725 | INSR | c.2842+17G>C (n.2842+17G>C) c.2806+17G>C (n.2806+17G>C) c.2920+17G>C (n.2920+17G>C) c.2884+17G>C (n.2884+17G>C) | gnomAD v4 |
19 | g.7132141C>T | CA631723696 | INSR | c.2842+17G>A (n.2842+17G>A) c.2806+17G>A (n.2806+17G>A) c.2920+17G>A (n.2920+17G>A) c.2884+17G>A (n.2884+17G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7132143dup | CA2587922726 | INSR | c.2842+15dup (n.2842+15dup) c.2806+15dup (n.2806+15dup) c.2920+15dup (n.2920+15dup) c.2884+15dup (n.2884+15dup) | gnomAD v4 |
19 | g.7132144C>T | CA2587922727 | INSR | c.2842+14G>A (n.2842+14G>A) c.2806+14G>A (n.2806+14G>A) c.2920+14G>A (n.2920+14G>A) c.2884+14G>A (n.2884+14G>A) | gnomAD v4 |
19 | g.7132145C>A | CA2541359340 | INSR | c.2842+13G>T (n.2842+13G>T) c.2806+13G>T (n.2806+13G>T) c.2920+13G>T (n.2920+13G>T) c.2884+13G>T (n.2884+13G>T) | |
19 | g.7132146A= | CA2320771041 | INSR | c.2842+12T= (n.2842+12T=) c.2806+12T= (n.2806+12T=) c.2920+12T= (n.2920+12T=) c.2884+12T= (n.2884+12T=) | |
19 | g.7132146A>C | CA2587922728 | INSR | c.2842+12T>G (n.2842+12T>G) c.2806+12T>G (n.2806+12T>G) c.2920+12T>G (n.2920+12T>G) c.2884+12T>G (n.2884+12T>G) | gnomAD v4 |
19 | g.7132146A>G | CA993109843 | INSR | c.2842+12T>C (n.2842+12T>C) c.2806+12T>C (n.2806+12T>C) c.2920+12T>C (n.2920+12T>C) c.2884+12T>C (n.2884+12T>C) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.7132147T>C | CA2587922729 | INSR | c.2842+11A>G (n.2842+11A>G) c.2806+11A>G (n.2806+11A>G) c.2920+11A>G (n.2920+11A>G) c.2884+11A>G (n.2884+11A>G) | gnomAD v4 |
19 | g.7132147T>G | CA2587922730 | INSR | c.2842+11A>C (n.2842+11A>C) c.2806+11A>C (n.2806+11A>C) c.2920+11A>C (n.2920+11A>C) c.2884+11A>C (n.2884+11A>C) | gnomAD v4 |
19 | g.7132148G>A | CA993109845 | INSR | c.2842+10C>T (n.2842+10C>T) c.2806+10C>T (n.2806+10C>T) c.2920+10C>T (n.2920+10C>T) c.2884+10C>T (n.2884+10C>T) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.7132148G= | CA2320771042 | INSR | c.2842+10C= (n.2842+10C=) c.2806+10C= (n.2806+10C=) c.2920+10C= (n.2920+10C=) c.2884+10C= (n.2884+10C=) | |
19 | g.7132148G>T | CA2587922731 | INSR | c.2842+10C>A (n.2842+10C>A) c.2806+10C>A (n.2806+10C>A) c.2920+10C>A (n.2920+10C>A) c.2884+10C>A (n.2884+10C>A) | gnomAD v4 |
19 | g.7132149G>C | CA2320771044 | INSR | c.2842+9C>G (n.2842+9C>G) c.2806+9C>G (n.2806+9C>G) c.2920+9C>G (n.2920+9C>G) c.2884+9C>G (n.2884+9C>G) | dbSNP |
19 | g.7132149G= | CA2320771043 | INSR | c.2842+9C= (n.2842+9C=) c.2806+9C= (n.2806+9C=) c.2920+9C= (n.2920+9C=) c.2884+9C= (n.2884+9C=) | |
19 | g.7132152A= | CA2320771045 | INSR | c.2842+6T= (n.2842+6T=) c.2806+6T= (n.2806+6T=) c.2920+6T= (n.2920+6T=) c.2884+6T= (n.2884+6T=) | |
19 | g.7132152A>G | CA2576595105 | INSR | c.2842+6T>C (n.2842+6T>C) c.2806+6T>C (n.2806+6T>C) c.2920+6T>C (n.2920+6T>C) c.2884+6T>C (n.2884+6T>C) | |
19 | g.7132152A>T | CA9135443 | INSR | c.2842+6T>A (n.2842+6T>A) c.2806+6T>A (n.2806+6T>A) c.2920+6T>A (n.2920+6T>A) c.2884+6T>A (n.2884+6T>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7132153C= | CA2320771046 | INSR | c.2842+5G= (n.2842+5G=) c.2806+5G= (n.2806+5G=) c.2920+5G= (n.2920+5G=) c.2884+5G= (n.2884+5G=) | |
19 | g.7132153C>T | CA631723697 | INSR | c.2842+5G>A (n.2842+5G>A) c.2806+5G>A (n.2806+5G>A) c.2920+5G>A (n.2920+5G>A) c.2884+5G>A (n.2884+5G>A) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.7132153dup | CA2838609413 | INSR | c.2842+5dup (n.2842+5dup) c.2806+5dup (n.2806+5dup) c.2920+5dup (n.2920+5dup) c.2884+5dup (n.2884+5dup) | |
19 | g.7132154T>A | CA9135444 | INSR | c.2842+4A>T (n.2842+4A>T) c.2806+4A>T (n.2806+4A>T) c.2920+4A>T (n.2920+4A>T) c.2884+4A>T (n.2884+4A>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7132154T= | CA2320771047 | INSR | c.2842+4A= (n.2842+4A=) c.2806+4A= (n.2806+4A=) c.2920+4A= (n.2920+4A=) c.2884+4A= (n.2884+4A=) | |
19 | g.7132155T>C | CA631723698 | INSR | c.2842+3A>G (n.2842+3A>G) c.2806+3A>G (n.2806+3A>G) c.2920+3A>G (n.2920+3A>G) c.2884+3A>G (n.2884+3A>G) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.7132155T>G | CA2576595106 | INSR | c.2842+3A>C (n.2842+3A>C) c.2806+3A>C (n.2806+3A>C) c.2920+3A>C (n.2920+3A>C) c.2884+3A>C (n.2884+3A>C) | |
19 | g.7132155T= | CA2320771048 | INSR | c.2842+3A= (n.2842+3A=) c.2806+3A= (n.2806+3A=) c.2920+3A= (n.2920+3A=) c.2884+3A= (n.2884+3A=) | |
19 | g.7132156A>C | CA403671889 | INSR | c.2842+2T>G (n.2842+2T>G) c.2806+2T>G (n.2806+2T>G) c.2920+2T>G (n.2920+2T>G) c.2884+2T>G (n.2884+2T>G) | |
19 | g.7132156A>G | CA403671890 | INSR | c.2842+2T>C (n.2842+2T>C) c.2806+2T>C (n.2806+2T>C) c.2920+2T>C (n.2920+2T>C) c.2884+2T>C (n.2884+2T>C) | |
19 | g.7132156A>T | CA403671891 | INSR | c.2842+2T>A (n.2842+2T>A) c.2806+2T>A (n.2806+2T>A) c.2920+2T>A (n.2920+2T>A) c.2884+2T>A (n.2884+2T>A) | |
19 | g.7132157C>A | CA403671892 | INSR | c.2842+1G>T (n.2842+1G>T) c.2806+1G>T (n.2806+1G>T) c.2920+1G>T (n.2920+1G>T) c.2884+1G>T (n.2884+1G>T) | |
19 | g.7132157C>G | CA403671893 | INSR | c.2842+1G>C (n.2842+1G>C) c.2806+1G>C (n.2806+1G>C) c.2920+1G>C (n.2920+1G>C) c.2884+1G>C (n.2884+1G>C) | |
19 | g.7132157C>T | CA403671894 | INSR | c.2842+1G>A (n.2842+1G>A) c.2806+1G>A (n.2806+1G>A) c.2920+1G>A (n.2920+1G>A) c.2884+1G>A (n.2884+1G>A) | |
19 | g.7132158A>C | CA403671895 | INSR | c.2842T>G (p.Leu948Val) c.2806T>G (p.Leu936Val) c.2920T>G (p.Tyr974Asp) c.2884T>G (p.Tyr962Asp) c.2842T>G (p.Tyr948Asp) c.2806T>G (p.Tyr936Asp) | |
19 | g.7132158A>G | CA505217438 | INSR | c.2842T>C (p.Leu948=) c.2806T>C (p.Leu936=) c.2920T>C (p.Tyr974His) c.2884T>C (p.Tyr962His) c.2842T>C (p.Tyr948His) c.2806T>C (p.Tyr936His) | |
19 | g.7132158A>T | CA403671896 | INSR | c.2842T>A (p.Leu948Ile) c.2806T>A (p.Leu936Ile) c.2920T>A (p.Tyr974Asn) c.2884T>A (p.Tyr962Asn) c.2842T>A (p.Tyr948Asn) c.2806T>A (p.Tyr936Asn) | |
19 | g.7132159A>C | CA403671897 | INSR | c.2841T>G (p.Tyr947Ter) c.2805T>G (p.Tyr935Ter) c.2919T>G (p.Tyr973Ter) c.2883T>G (p.Tyr961Ter) | |
19 | g.7132159A>G | CA505217439 | INSR | c.2841T>C (p.Tyr947=) c.2805T>C (p.Tyr935=) c.2919T>C (p.Tyr973=) c.2883T>C (p.Tyr961=) | |
19 | g.7132159A>T | CA403671898 | INSR | c.2841T>A (p.Tyr947Ter) c.2805T>A (p.Tyr935Ter) c.2919T>A (p.Tyr973Ter) c.2883T>A (p.Tyr961Ter) | |
19 | g.7132160T>A | CA403671899 | INSR | c.2840A>T (p.Tyr947Phe) c.2804A>T (p.Tyr935Phe) c.2918A>T (p.Tyr973Phe) c.2882A>T (p.Tyr961Phe) | |
19 | g.7132160T>C | CA403671900 | INSR | c.2840A>G (p.Tyr947Cys) c.2804A>G (p.Tyr935Cys) c.2918A>G (p.Tyr973Cys) c.2882A>G (p.Tyr961Cys) | |
19 | g.7132160T>G | CA403671901 | INSR | c.2840A>C (p.Tyr947Ser) c.2804A>C (p.Tyr935Ser) c.2918A>C (p.Tyr973Ser) c.2882A>C (p.Tyr961Ser) | |
19 | g.7132161A>C | CA403671902 | INSR | c.2839T>G (p.Tyr947Asp) c.2803T>G (p.Tyr935Asp) c.2917T>G (p.Tyr973Asp) c.2881T>G (p.Tyr961Asp) | |
19 | g.7132161A>G | CA403671903 | INSR | c.2839T>C (p.Tyr947His) c.2803T>C (p.Tyr935His) c.2917T>C (p.Tyr973His) c.2881T>C (p.Tyr961His) | |
19 | g.7132161A>T | CA403671904 | INSR | c.2839T>A (p.Tyr947Asn) c.2803T>A (p.Tyr935Asn) c.2917T>A (p.Tyr973Asn) c.2881T>A (p.Tyr961Asn) | |
19 | g.7132162G>A | CA505217440 | INSR | c.2838C>T (p.Asp946=) c.2802C>T (p.Asp934=) c.2916C>T (p.Asp972=) c.2880C>T (p.Asp960=) | |
19 | g.7132162G>C | CA208959 | INSR | c.2838C>G (p.Asp946Glu) c.2802C>G (p.Asp934Glu) c.2916C>G (p.Asp972Glu) c.2880C>G (p.Asp960Glu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7132162G= | CA2320771049 | INSR | c.2838C= (p.Asp946=) c.2802C= (p.Asp934=) c.2916C= (p.Asp972=) c.2880C= (p.Asp960=) | |
19 | g.7132162G>T | CA403671905 | INSR | c.2838C>A (p.Asp946Glu) c.2802C>A (p.Asp934Glu) c.2916C>A (p.Asp972Glu) c.2880C>A (p.Asp960Glu) | |
19 | g.7132163T>A | CA403671906 | INSR | c.2837A>T (p.Asp946Val) c.2801A>T (p.Asp934Val) c.2915A>T (p.Asp972Val) c.2879A>T (p.Asp960Val) | gnomAD v4 |
19 | g.7132163T>C | CA403671907 | INSR | c.2837A>G (p.Asp946Gly) c.2801A>G (p.Asp934Gly) c.2915A>G (p.Asp972Gly) c.2879A>G (p.Asp960Gly) | |
19 | g.7132163T>G | CA403671908 | INSR | c.2837A>C (p.Asp946Ala) c.2801A>C (p.Asp934Ala) c.2915A>C (p.Asp972Ala) c.2879A>C (p.Asp960Ala) | |
19 | g.7132164C>A | CA403671910 | INSR | c.2836G>T (p.Asp946Tyr) c.2800G>T (p.Asp934Tyr) c.2914G>T (p.Asp972Tyr) c.2878G>T (p.Asp960Tyr) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.7132164C= | CA2320771050 | INSR | c.2836G= (p.Asp946=) c.2800G= (p.Asp934=) c.2914G= (p.Asp972=) c.2878G= (p.Asp960=) | |
19 | g.7132164C>G | CA403671911 | INSR | c.2836G>C (p.Asp946His) c.2800G>C (p.Asp934His) c.2914G>C (p.Asp972His) c.2878G>C (p.Asp960His) | |
19 | g.7132164C>T | CA403671909 | INSR | c.2836G>A (p.Asp946Asn) c.2800G>A (p.Asp934Asn) c.2914G>A (p.Asp972Asn) c.2878G>A (p.Asp960Asn) | COSMIC COSMIC |
19 | g.7132165T>A | CA505217441 | INSR | c.2835A>T (p.Thr945=) c.2799A>T (p.Thr933=) c.2913A>T (p.Thr971=) c.2877A>T (p.Thr959=) | |
19 | g.7132165T>C | CA505217442 | INSR | c.2835A>G (p.Thr945=) c.2799A>G (p.Thr933=) c.2913A>G (p.Thr971=) c.2877A>G (p.Thr959=) | |
19 | g.7132165T>G | CA505217443 | INSR | c.2835A>C (p.Thr945=) c.2799A>C (p.Thr933=) c.2913A>C (p.Thr971=) c.2877A>C (p.Thr959=) | |
19 | g.7132166G>A | CA403671912 | INSR | c.2834C>T (p.Thr945Ile) c.2798C>T (p.Thr933Ile) c.2912C>T (p.Thr971Ile) c.2876C>T (p.Thr959Ile) | gnomAD v4 |
19 | g.7132166G>C | CA403671913 | INSR | c.2834C>G (p.Thr945Arg) c.2798C>G (p.Thr933Arg) c.2912C>G (p.Thr971Arg) c.2876C>G (p.Thr959Arg) | |
19 | g.7132166G>T | CA403671914 | INSR | c.2834C>A (p.Thr945Lys) c.2798C>A (p.Thr933Lys) c.2912C>A (p.Thr971Lys) c.2876C>A (p.Thr959Lys) | |
19 | g.7132167T>A | CA403671915 | INSR | c.2833A>T (p.Thr945Ser) c.2797A>T (p.Thr933Ser) c.2911A>T (p.Thr971Ser) c.2875A>T (p.Thr959Ser) | gnomAD v4 |
19 | g.7132167T>C | CA403671916 | INSR | c.2833A>G (p.Thr945Ala) c.2797A>G (p.Thr933Ala) c.2911A>G (p.Thr971Ala) c.2875A>G (p.Thr959Ala) | gnomAD v4 |
19 | g.7132167T>G | CA403671917 | INSR | c.2833A>C (p.Thr945Pro) c.2797A>C (p.Thr933Pro) c.2911A>C (p.Thr971Pro) c.2875A>C (p.Thr959Pro) | |
19 | g.7132168C>A | CA505217445 | INSR | c.2832G>T (p.Val944=) c.2796G>T (p.Val932=) c.2910G>T (p.Val970=) c.2874G>T (p.Val958=) | gnomAD v4 |
19 | g.7132168C= | CA2320771051 | INSR | c.2832G= (p.Val944=) c.2796G= (p.Val932=) c.2910G= (p.Val970=) c.2874G= (p.Val958=) | |
19 | g.7132168C>G | CA505217444 | INSR | c.2832G>C (p.Val944=) c.2796G>C (p.Val932=) c.2910G>C (p.Val970=) c.2874G>C (p.Val958=) | dbSNP gnomAD v2 |
19 | g.7132168C>T | CA9135445 | INSR | c.2832G>A (p.Val944=) c.2796G>A (p.Val932=) c.2910G>A (p.Val970=) c.2874G>A (p.Val958=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.7132169A>C | CA403671918 | INSR | c.2831T>G (p.Val944Gly) c.2795T>G (p.Val932Gly) c.2909T>G (p.Val970Gly) c.2873T>G (p.Val958Gly) | |
19 | g.7132169A>G | CA403671919 | INSR | c.2831T>C (p.Val944Ala) c.2795T>C (p.Val932Ala) c.2909T>C (p.Val970Ala) c.2873T>C (p.Val958Ala) | |
19 | g.7132169A>T | CA403671920 | INSR | c.2831T>A (p.Val944Glu) c.2795T>A (p.Val932Glu) c.2909T>A (p.Val970Glu) c.2873T>A (p.Val958Glu) | |
19 | g.7132170C>A | CA403671921 | INSR | c.2830G>T (p.Val944Leu) c.2794G>T (p.Val932Leu) c.2908G>T (p.Val970Leu) c.2872G>T (p.Val958Leu) | |
19 | g.7132170C= | CA2320771052 | INSR | c.2830G= (p.Val944=) c.2794G= (p.Val932=) c.2908G= (p.Val970=) c.2872G= (p.Val958=) | |
19 | g.7132170C>G | CA403671922 | INSR | c.2830G>C (p.Val944Leu) c.2794G>C (p.Val932Leu) c.2908G>C (p.Val970Leu) c.2872G>C (p.Val958Leu) | ClinVar |
19 | g.7132170C>T | CA9135446 | INSR | c.2830G>A (p.Val944Met) c.2794G>A (p.Val932Met) c.2908G>A (p.Val970Met) c.2872G>A (p.Val958Met) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7132171G>A | CA9135447 | INSR | c.2829C>T (p.Tyr943=) c.2793C>T (p.Tyr931=) c.2907C>T (p.Tyr969=) c.2871C>T (p.Tyr957=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
19 | g.7132171G>C | CA403671924 | INSR | c.2829C>G (p.Tyr943Ter) c.2793C>G (p.Tyr931Ter) c.2907C>G (p.Tyr969Ter) c.2871C>G (p.Tyr957Ter) | |
19 | g.7132171G= | CA2320771053 | INSR | c.2829C= (p.Tyr943=) c.2793C= (p.Tyr931=) c.2907C= (p.Tyr969=) c.2871C= (p.Tyr957=) | |
19 | g.7132171G>T | CA403671923 | INSR | c.2829C>A (p.Tyr943Ter) c.2793C>A (p.Tyr931Ter) c.2907C>A (p.Tyr969Ter) c.2871C>A (p.Tyr957Ter) | |
19 | g.7132172T>A | CA403671925 | INSR | c.2828A>T (p.Tyr943Phe) c.2792A>T (p.Tyr931Phe) c.2906A>T (p.Tyr969Phe) c.2870A>T (p.Tyr957Phe) | dbSNP |
19 | g.7132172T>C | CA403671927 | INSR | c.2828A>G (p.Tyr943Cys) c.2792A>G (p.Tyr931Cys) c.2906A>G (p.Tyr969Cys) c.2870A>G (p.Tyr957Cys) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.7132172T>G | CA403671926 | INSR | c.2828A>C (p.Tyr943Ser) c.2792A>C (p.Tyr931Ser) c.2906A>C (p.Tyr969Ser) c.2870A>C (p.Tyr957Ser) | |
19 | g.7132172T= | CA2320771054 | INSR | c.2828A= (p.Tyr943=) c.2792A= (p.Tyr931=) c.2906A= (p.Tyr969=) c.2870A= (p.Tyr957=) | |
19 | g.7132173A>C | CA403671928 | INSR | c.2827T>G (p.Tyr943Asp) c.2791T>G (p.Tyr931Asp) c.2905T>G (p.Tyr969Asp) c.2869T>G (p.Tyr957Asp) | gnomAD v4 |
19 | g.7132173A>G | CA403671929 | INSR | c.2827T>C (p.Tyr943His) c.2791T>C (p.Tyr931His) c.2905T>C (p.Tyr969His) c.2869T>C (p.Tyr957His) | |
19 | g.7132173A>T | CA403671930 | INSR | c.2827T>A (p.Tyr943Asn) c.2791T>A (p.Tyr931Asn) c.2905T>A (p.Tyr969Asn) c.2869T>A (p.Tyr957Asn) | |
19 | g.7132174G>A | CA505217446 | INSR | c.2826C>T (p.Phe942=) c.2790C>T (p.Phe930=) c.2904C>T (p.Phe968=) c.2868C>T (p.Phe956=) | gnomAD v4 |
19 | g.7132174G>C | CA304878369 | INSR | c.2826C>G (p.Phe942Leu) c.2790C>G (p.Phe930Leu) c.2904C>G (p.Phe968Leu) c.2868C>G (p.Phe956Leu) | dbSNP |
19 | g.7132174G= | CA2320771055 | INSR | c.2826C= (p.Phe942=) c.2790C= (p.Phe930=) c.2904C= (p.Phe968=) c.2868C= (p.Phe956=) | |
19 | g.7132174G>T | CA403671931 | INSR | c.2826C>A (p.Phe942Leu) c.2790C>A (p.Phe930Leu) c.2904C>A (p.Phe968Leu) c.2868C>A (p.Phe956Leu) | |
19 | g.7132175A>C | CA403671932 | INSR | c.2825T>G (p.Phe942Cys) c.2789T>G (p.Phe930Cys) c.2903T>G (p.Phe968Cys) c.2867T>G (p.Phe956Cys) | |
19 | g.7132175A>G | CA403671933 | INSR | c.2825T>C (p.Phe942Ser) c.2789T>C (p.Phe930Ser) c.2903T>C (p.Phe968Ser) c.2867T>C (p.Phe956Ser) | |
19 | g.7132175A>T | CA403671934 | INSR | c.2825T>A (p.Phe942Tyr) c.2789T>A (p.Phe930Tyr) c.2903T>A (p.Phe968Tyr) c.2867T>A (p.Phe956Tyr) | |
19 | g.7132176A>C | CA403671935 | INSR | c.2824T>G (p.Phe942Val) c.2788T>G (p.Phe930Val) c.2902T>G (p.Phe968Val) c.2866T>G (p.Phe956Val) | |
19 | g.7132176A>G | CA403671936 | INSR | c.2824T>C (p.Phe942Leu) c.2788T>C (p.Phe930Leu) c.2902T>C (p.Phe968Leu) c.2866T>C (p.Phe956Leu) | gnomAD v4 |
19 | g.7132176A>T | CA403671937 | INSR | c.2824T>A (p.Phe942Ile) c.2788T>A (p.Phe930Ile) c.2902T>A (p.Phe968Ile) c.2866T>A (p.Phe956Ile) | |
19 | g.7132177A>C | CA403671938 | INSR | c.2823T>G (p.Tyr941Ter) c.2787T>G (p.Tyr929Ter) c.2901T>G (p.Tyr967Ter) c.2865T>G (p.Tyr955Ter) | |
19 | g.7132177A>G | CA505217447 | INSR | c.2823T>C (p.Tyr941=) c.2787T>C (p.Tyr929=) c.2901T>C (p.Tyr967=) c.2865T>C (p.Tyr955=) | |
19 | g.7132177A>T | CA403671939 | INSR | c.2823T>A (p.Tyr941Ter) c.2787T>A (p.Tyr929Ter) c.2901T>A (p.Tyr967Ter) c.2865T>A (p.Tyr955Ter) | |
19 | g.7132178T>A | CA403671940 | INSR | c.2822A>T (p.Tyr941Phe) c.2786A>T (p.Tyr929Phe) c.2900A>T (p.Tyr967Phe) c.2864A>T (p.Tyr955Phe) | |
19 | g.7132178T>C | CA403671942 | INSR | c.2822A>G (p.Tyr941Cys) c.2786A>G (p.Tyr929Cys) c.2900A>G (p.Tyr967Cys) c.2864A>G (p.Tyr955Cys) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7132178T>G | CA403671941 | INSR | c.2822A>C (p.Tyr941Ser) c.2786A>C (p.Tyr929Ser) c.2900A>C (p.Tyr967Ser) c.2864A>C (p.Tyr955Ser) | |
19 | g.7132178T= | CA2320771056 | INSR | c.2822A= (p.Tyr941=) c.2786A= (p.Tyr929=) c.2900A= (p.Tyr967=) c.2864A= (p.Tyr955=) | |
19 | g.7132179A>C | CA403671943 | INSR | c.2821T>G (p.Tyr941Asp) c.2785T>G (p.Tyr929Asp) c.2899T>G (p.Tyr967Asp) c.2863T>G (p.Tyr955Asp) | |
19 | g.7132179A>G | CA403671944 | INSR | c.2821T>C (p.Tyr941His) c.2785T>C (p.Tyr929His) c.2899T>C (p.Tyr967His) c.2863T>C (p.Tyr955His) | |
19 | g.7132179A>T | CA403671945 | INSR | c.2821T>A (p.Tyr941Asn) c.2785T>A (p.Tyr929Asn) c.2899T>A (p.Tyr967Asn) c.2863T>A (p.Tyr955Asn) | gnomAD v4 |
19 | g.7132180G>A | CA505217448 | INSR | c.2820C>T (p.Thr940=) c.2784C>T (p.Thr928=) c.2898C>T (p.Thr966=) c.2862C>T (p.Thr954=) | |
19 | g.7132180G>C | CA505217449 | INSR | c.2820C>G (p.Thr940=) c.2784C>G (p.Thr928=) c.2898C>G (p.Thr966=) c.2862C>G (p.Thr954=) | gnomAD v4 |
19 | g.7132180G>T | CA505217450 | INSR | c.2820C>A (p.Thr940=) c.2784C>A (p.Thr928=) c.2898C>A (p.Thr966=) c.2862C>A (p.Thr954=) | |
19 | g.7132181G>A | CA403671946 | INSR | c.2819C>T (p.Thr940Ile) c.2783C>T (p.Thr928Ile) c.2897C>T (p.Thr966Ile) c.2861C>T (p.Thr954Ile) | |
19 | g.7132181G>C | CA403671947 | INSR | c.2819C>G (p.Thr940Ser) c.2783C>G (p.Thr928Ser) c.2897C>G (p.Thr966Ser) c.2861C>G (p.Thr954Ser) | |
19 | g.7132181G>T | CA403671948 | INSR | c.2819C>A (p.Thr940Asn) c.2783C>A (p.Thr928Asn) c.2897C>A (p.Thr966Asn) c.2861C>A (p.Thr954Asn) | |
19 | g.7132182T>A | CA403671949 | INSR | c.2818A>T (p.Thr940Ser) c.2782A>T (p.Thr928Ser) c.2896A>T (p.Thr966Ser) c.2860A>T (p.Thr954Ser) | |
19 | g.7132182T>C | CA403671950 | INSR | c.2818A>G (p.Thr940Ala) c.2782A>G (p.Thr928Ala) c.2896A>G (p.Thr966Ala) c.2860A>G (p.Thr954Ala) | |
19 | g.7132182T>G | CA403671951 | INSR | c.2818A>C (p.Thr940Pro) c.2782A>C (p.Thr928Pro) c.2896A>C (p.Thr966Pro) c.2860A>C (p.Thr954Pro) | |
19 | g.7132183G>A | CA505217453 | INSR | c.2817C>T (p.Pro939=) c.2781C>T (p.Pro927=) c.2895C>T (p.Pro965=) c.2859C>T (p.Pro953=) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.7132183G>C | CA505217451 | INSR | c.2817C>G (p.Pro939=) c.2781C>G (p.Pro927=) c.2895C>G (p.Pro965=) c.2859C>G (p.Pro953=) | |
19 | g.7132183G= | CA2320771057 | INSR | c.2817C= (p.Pro939=) c.2781C= (p.Pro927=) c.2895C= (p.Pro965=) c.2859C= (p.Pro953=) | |
19 | g.7132183G>T | CA505217452 | INSR | c.2817C>A (p.Pro939=) c.2781C>A (p.Pro927=) c.2895C>A (p.Pro965=) c.2859C>A (p.Pro953=) | |
19 | g.7132185dup | CA2840890619 | INSR | c.2817dup (p.Thr940HisfsTer?) c.2781dup (p.Thr928HisfsTer?) c.2895dup (p.Thr966HisfsTer?) c.2859dup (p.Thr954HisfsTer?) | |
19 | g.7132184G>A | CA403671954 | INSR | c.2816C>T (p.Pro939Leu) c.2780C>T (p.Pro927Leu) c.2894C>T (p.Pro965Leu) c.2858C>T (p.Pro953Leu) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7132184G>C | CA403671953 | INSR | c.2816C>G (p.Pro939Arg) c.2780C>G (p.Pro927Arg) c.2894C>G (p.Pro965Arg) c.2858C>G (p.Pro953Arg) | |
19 | g.7132184G= | CA2320771058 | INSR | c.2816C= (p.Pro939=) c.2780C= (p.Pro927=) c.2894C= (p.Pro965=) c.2858C= (p.Pro953=) | |
19 | g.7132184G>T | CA403671952 | INSR | c.2816C>A (p.Pro939His) c.2780C>A (p.Pro927His) c.2894C>A (p.Pro965His) c.2858C>A (p.Pro953His) | gnomAD v4 |
19 | g.7132185G>A | CA403671955 | INSR | c.2815C>T (p.Pro939Ser) c.2779C>T (p.Pro927Ser) c.2893C>T (p.Pro965Ser) c.2857C>T (p.Pro953Ser) | |
19 | g.7132185G>C | CA403671956 | INSR | c.2815C>G (p.Pro939Ala) c.2779C>G (p.Pro927Ala) c.2893C>G (p.Pro965Ala) c.2857C>G (p.Pro953Ala) | |
19 | g.7132185G= | CA2320771059 | INSR | c.2815C= (p.Pro939=) c.2779C= (p.Pro927=) c.2893C= (p.Pro965=) c.2857C= (p.Pro953=) | |
19 | g.7132185G>T | CA403671957 | INSR | c.2815C>A (p.Pro939Thr) c.2779C>A (p.Pro927Thr) c.2893C>A (p.Pro965Thr) c.2857C>A (p.Pro953Thr) | dbSNP |
19 | g.7132186T>A | CA403671958 | INSR | c.2814A>T (p.Glu938Asp) c.2778A>T (p.Glu926Asp) c.2892A>T (p.Glu964Asp) c.2856A>T (p.Glu952Asp) | |
19 | g.7132186T>C | CA9135448 | INSR | c.2814A>G (p.Glu938=) c.2778A>G (p.Glu926=) c.2892A>G (p.Glu964=) c.2856A>G (p.Glu952=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.7132186T>G | CA403671959 | INSR | c.2814A>C (p.Glu938Asp) c.2778A>C (p.Glu926Asp) c.2892A>C (p.Glu964Asp) c.2856A>C (p.Glu952Asp) | dbSNP |
19 | g.7132186T= | CA2320771060 | INSR | c.2814A= (p.Glu938=) c.2778A= (p.Glu926=) c.2892A= (p.Glu964=) c.2856A= (p.Glu952=) | |
19 | g.7132187T>A | CA403671960 | INSR | c.2813A>T (p.Glu938Val) c.2777A>T (p.Glu926Val) c.2891A>T (p.Glu964Val) c.2855A>T (p.Glu952Val) | |
19 | g.7132187T>C | CA403671961 | INSR | c.2813A>G (p.Glu938Gly) c.2777A>G (p.Glu926Gly) c.2891A>G (p.Glu964Gly) c.2855A>G (p.Glu952Gly) | |
19 | g.7132187T>G | CA403671962 | INSR | c.2813A>C (p.Glu938Ala) c.2777A>C (p.Glu926Ala) c.2891A>C (p.Glu964Ala) c.2855A>C (p.Glu952Ala) | |
19 | g.7132188C>A | CA403671963 | INSR | c.2812G>T (p.Glu938Ter) c.2776G>T (p.Glu926Ter) c.2890G>T (p.Glu964Ter) c.2854G>T (p.Glu952Ter) | |
19 | g.7132188C>G | CA403671964 | INSR | c.2812G>C (p.Glu938Gln) c.2776G>C (p.Glu926Gln) c.2890G>C (p.Glu964Gln) c.2854G>C (p.Glu952Gln) | |
19 | g.7132188C>T | CA403671965 | INSR | c.2812G>A (p.Glu938Lys) c.2776G>A (p.Glu926Lys) c.2890G>A (p.Glu964Lys) c.2854G>A (p.Glu952Lys) | gnomAD v4 |
19 | g.7132189del | CA2545872211 | INSR | c.2812del (p.Glu938AsnfsTer7) c.2776del (p.Glu926AsnfsTer7) c.2890del (p.Glu964AsnfsTer7) c.2854del (p.Glu952AsnfsTer7) | |
19 | g.7132189C>A | CA505217455 | INSR | c.2811G>T (p.Thr937=) c.2775G>T (p.Thr925=) c.2889G>T (p.Thr963=) c.2853G>T (p.Thr951=) | |
19 | g.7132189C= | CA2320771061 | INSR | c.2811G= (p.Thr937=) c.2775G= (p.Thr925=) c.2889G= (p.Thr963=) c.2853G= (p.Thr951=) | |
19 | g.7132189C>G | CA505217456 | INSR | c.2811G>C (p.Thr937=) c.2775G>C (p.Thr925=) c.2889G>C (p.Thr963=) c.2853G>C (p.Thr951=) | |
19 | g.7132189C>T | CA9135449 | INSR | c.2811G>A (p.Thr937=) c.2775G>A (p.Thr925=) c.2889G>A (p.Thr963=) c.2853G>A (p.Thr951=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7132190G>A | CA403671968 | INSR | c.2810C>T (p.Thr937Met) c.2774C>T (p.Thr925Met) c.2888C>T (p.Thr963Met) c.2852C>T (p.Thr951Met) | ClinVar dbSNP gnomAD v4 |
19 | g.7132190G>C | CA403671966 | INSR | c.2810C>G (p.Thr937Arg) c.2774C>G (p.Thr925Arg) c.2888C>G (p.Thr963Arg) c.2852C>G (p.Thr951Arg) | |
19 | g.7132190G= | CA2320771062 | INSR | c.2810C= (p.Thr937=) c.2774C= (p.Thr925=) c.2888C= (p.Thr963=) c.2852C= (p.Thr951=) | |
19 | g.7132190G>T | CA403671967 | INSR | c.2810C>A (p.Thr937Lys) c.2774C>A (p.Thr925Lys) c.2888C>A (p.Thr963Lys) c.2852C>A (p.Thr951Lys) | |
19 | g.7132191T>A | CA403671969 | INSR | c.2809A>T (p.Thr937Ser) c.2773A>T (p.Thr925Ser) c.2887A>T (p.Thr963Ser) c.2851A>T (p.Thr951Ser) | |
19 | g.7132191T>C | CA403671970 | INSR | c.2809A>G (p.Thr937Ala) c.2773A>G (p.Thr925Ala) c.2887A>G (p.Thr963Ala) c.2851A>G (p.Thr951Ala) | |
19 | g.7132191T>G | CA403671971 | INSR | c.2809A>C (p.Thr937Pro) c.2773A>C (p.Thr925Pro) c.2887A>C (p.Thr963Pro) c.2851A>C (p.Thr951Pro) | |
19 | g.7132192C>A | CA403671972 | INSR | c.2808G>T (p.Trp936Cys) c.2772G>T (p.Trp924Cys) c.2886G>T (p.Trp962Cys) c.2850G>T (p.Trp950Cys) | |
19 | g.7132192C>G | CA403671973 | INSR | c.2808G>C (p.Trp936Cys) c.2772G>C (p.Trp924Cys) c.2886G>C (p.Trp962Cys) c.2850G>C (p.Trp950Cys) | |
19 | g.7132192C>T | CA403671974 | INSR | c.2808G>A (p.Trp936Ter) c.2772G>A (p.Trp924Ter) c.2886G>A (p.Trp962Ter) c.2850G>A (p.Trp950Ter) | |
19 | g.7132193C>A | CA403671975 | INSR | c.2807G>T (p.Trp936Leu) c.2771G>T (p.Trp924Leu) c.2885G>T (p.Trp962Leu) c.2849G>T (p.Trp950Leu) | |
19 | g.7132193C>G | CA403671976 | INSR | c.2807G>C (p.Trp936Ser) c.2771G>C (p.Trp924Ser) c.2885G>C (p.Trp962Ser) c.2849G>C (p.Trp950Ser) | |
19 | g.7132193C>T | CA403671977 | INSR | c.2807G>A (p.Trp936Ter) c.2771G>A (p.Trp924Ter) c.2885G>A (p.Trp962Ter) c.2849G>A (p.Trp950Ter) | |
19 | g.7132194A>C | CA403671978 | INSR | c.2806T>G (p.Trp936Gly) c.2770T>G (p.Trp924Gly) c.2884T>G (p.Trp962Gly) c.2848T>G (p.Trp950Gly) | |
19 | g.7132194A>G | CA403671979 | INSR | c.2806T>C (p.Trp936Arg) c.2770T>C (p.Trp924Arg) c.2884T>C (p.Trp962Arg) c.2848T>C (p.Trp950Arg) | |
19 | g.7132194A>T | CA403671980 | INSR | c.2806T>A (p.Trp936Arg) c.2770T>A (p.Trp924Arg) c.2884T>A (p.Trp962Arg) c.2848T>A (p.Trp950Arg) | |
19 | g.7132195A>C | CA505217460 | INSR | c.2805T>G (p.Ser935=) c.2769T>G (p.Ser923=) c.2883T>G (p.Ser961=) c.2847T>G (p.Ser949=) | |
19 | g.7132195A>G | CA505217461 | INSR | c.2805T>C (p.Ser935=) c.2769T>C (p.Ser923=) c.2883T>C (p.Ser961=) c.2847T>C (p.Ser949=) | gnomAD v4 |
19 | g.7132195A>T | CA505217462 | INSR | c.2805T>A (p.Ser935=) c.2769T>A (p.Ser923=) c.2883T>A (p.Ser961=) c.2847T>A (p.Ser949=) | |
19 | g.7132196G>A | CA403671983 | INSR | c.2804C>T (p.Ser935Phe) c.2768C>T (p.Ser923Phe) c.2882C>T (p.Ser961Phe) c.2846C>T (p.Ser949Phe) | |
19 | g.7132196G>C | CA403671982 | INSR | c.2804C>G (p.Ser935Cys) c.2768C>G (p.Ser923Cys) c.2882C>G (p.Ser961Cys) c.2846C>G (p.Ser949Cys) | |
19 | g.7132196G>T | CA403671981 | INSR | c.2804C>A (p.Ser935Tyr) c.2768C>A (p.Ser923Tyr) c.2882C>A (p.Ser961Tyr) c.2846C>A (p.Ser949Tyr) | |
19 | g.7132197A= | CA2320771063 | INSR | c.2803T= (p.Ser935=) c.2767T= (p.Ser923=) c.2881T= (p.Ser961=) c.2845T= (p.Ser949=) | |
19 | g.7132197A>C | CA403671985 | INSR | c.2803T>G (p.Ser935Ala) c.2767T>G (p.Ser923Ala) c.2881T>G (p.Ser961Ala) c.2845T>G (p.Ser949Ala) | |
19 | g.7132197A>G | CA403671984 | INSR | c.2803T>C (p.Ser935Pro) c.2767T>C (p.Ser923Pro) c.2881T>C (p.Ser961Pro) c.2845T>C (p.Ser949Pro) | |
19 | g.7132197A>T | CA403671986 | INSR | c.2803T>A (p.Ser935Thr) c.2767T>A (p.Ser923Thr) c.2881T>A (p.Ser961Thr) c.2845T>A (p.Ser949Thr) | dbSNP |
19 | g.7132198G>A | CA505217468 | INSR | c.2802C>T (p.Gly934=) c.2766C>T (p.Gly922=) c.2880C>T (p.Gly960=) c.2844C>T (p.Gly948=) | |
19 | g.7132198G>C | CA505217470 | INSR | c.2802C>G (p.Gly934=) c.2766C>G (p.Gly922=) c.2880C>G (p.Gly960=) c.2844C>G (p.Gly948=) | |
19 | g.7132198G>T | CA505217471 | INSR | c.2802C>A (p.Gly934=) c.2766C>A (p.Gly922=) c.2880C>A (p.Gly960=) c.2844C>A (p.Gly948=) | |
19 | g.7132199C>A | CA403671987 | INSR | c.2801G>T (p.Gly934Val) c.2765G>T (p.Gly922Val) c.2879G>T (p.Gly960Val) c.2843G>T (p.Gly948Val) | |
19 | g.7132199C>G | CA403671989 | INSR | c.2801G>C (p.Gly934Ala) c.2765G>C (p.Gly922Ala) c.2879G>C (p.Gly960Ala) c.2843G>C (p.Gly948Ala) | |
19 | g.7132199C>T | CA403671988 | INSR | c.2801G>A (p.Gly934Asp) c.2765G>A (p.Gly922Asp) c.2879G>A (p.Gly960Asp) c.2843G>A (p.Gly948Asp) | |
19 | g.7132200C>A | CA403671990 | INSR | c.2800G>T (p.Gly934Cys) c.2764G>T (p.Gly922Cys) c.2878G>T (p.Gly960Cys) c.2842G>T (p.Gly948Cys) | |
19 | g.7132200C= | CA2320771064 | INSR | c.2800G= (p.Gly934=) c.2764G= (p.Gly922=) c.2878G= (p.Gly960=) c.2842G= (p.Gly948=) | |
19 | g.7132200C>G | CA403671991 | INSR | c.2800G>C (p.Gly934Arg) c.2764G>C (p.Gly922Arg) c.2878G>C (p.Gly960Arg) c.2842G>C (p.Gly948Arg) | |
19 | g.7132200C>T | CA403671992 | INSR | c.2800G>A (p.Gly934Ser) c.2764G>A (p.Gly922Ser) c.2878G>A (p.Gly960Ser) c.2842G>A (p.Gly948Ser) | dbSNP gnomAD v4 |
19 | g.7132201G>A | CA9135450 | INSR | c.2799C>T (p.Asn933=) c.2763C>T (p.Asn921=) c.2877C>T (p.Asn959=) c.2841C>T (p.Asn947=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7132201G>C | CA403671993 | INSR | c.2799C>G (p.Asn933Lys) c.2763C>G (p.Asn921Lys) c.2877C>G (p.Asn959Lys) c.2841C>G (p.Asn947Lys) | |
19 | g.7132201G= | CA2320771065 | INSR | c.2799C= (p.Asn933=) c.2763C= (p.Asn921=) c.2877C= (p.Asn959=) c.2841C= (p.Asn947=) | |
19 | g.7132201G>T | CA403671994 | INSR | c.2799C>A (p.Asn933Lys) c.2763C>A (p.Asn921Lys) c.2877C>A (p.Asn959Lys) c.2841C>A (p.Asn947Lys) | |
19 | g.7132202T>A | CA403671997 | INSR | c.2798A>T (p.Asn933Ile) c.2762A>T (p.Asn921Ile) c.2876A>T (p.Asn959Ile) c.2840A>T (p.Asn947Ile) | |
19 | g.7132202T>C | CA403671996 | INSR | c.2798A>G (p.Asn933Ser) c.2762A>G (p.Asn921Ser) c.2876A>G (p.Asn959Ser) c.2840A>G (p.Asn947Ser) | |
19 | g.7132202T>G | CA403671995 | INSR | c.2798A>C (p.Asn933Thr) c.2762A>C (p.Asn921Thr) c.2876A>C (p.Asn959Thr) c.2840A>C (p.Asn947Thr) | |
19 | g.7132203T>A | CA403671998 | INSR | c.2797A>T (p.Asn933Tyr) c.2761A>T (p.Asn921Tyr) c.2875A>T (p.Asn959Tyr) c.2839A>T (p.Asn947Tyr) | COSMIC COSMIC |
19 | g.7132203T>C | CA403671999 | INSR | c.2797A>G (p.Asn933Asp) c.2761A>G (p.Asn921Asp) c.2875A>G (p.Asn959Asp) c.2839A>G (p.Asn947Asp) | |
19 | g.7132203T>G | CA403672000 | INSR | c.2797A>C (p.Asn933His) c.2761A>C (p.Asn921His) c.2875A>C (p.Asn959His) c.2839A>C (p.Asn947His) | |
19 | g.7132204G>A | CA505217477 | INSR | c.2796C>T (p.Gly932=) c.2760C>T (p.Gly920=) c.2874C>T (p.Gly958=) c.2838C>T (p.Gly946=) | |
19 | g.7132204G>C | CA505217480 | INSR | c.2796C>G (p.Gly932=) c.2760C>G (p.Gly920=) c.2874C>G (p.Gly958=) c.2838C>G (p.Gly946=) | |
19 | g.7132204G>T | CA505217478 | INSR | c.2796C>A (p.Gly932=) c.2760C>A (p.Gly920=) c.2874C>A (p.Gly958=) c.2838C>A (p.Gly946=) | |
19 | g.7132205C>A | CA403672001 | INSR | c.2795G>T (p.Gly932Val) c.2759G>T (p.Gly920Val) c.2873G>T (p.Gly958Val) c.2837G>T (p.Gly946Val) | |
19 | g.7132205C>G | CA403672002 | INSR | c.2795G>C (p.Gly932Ala) c.2759G>C (p.Gly920Ala) c.2873G>C (p.Gly958Ala) c.2837G>C (p.Gly946Ala) | |
19 | g.7132205C>T | CA403672003 | INSR | c.2795G>A (p.Gly932Asp) c.2759G>A (p.Gly920Asp) c.2873G>A (p.Gly958Asp) c.2837G>A (p.Gly946Asp) | gnomAD v4 |
19 | g.7132206C>A | CA403672004 | INSR | c.2794G>T (p.Gly932Cys) c.2758G>T (p.Gly920Cys) c.2872G>T (p.Gly958Cys) c.2836G>T (p.Gly946Cys) | |
19 | g.7132206C>G | CA403672006 | INSR | c.2794G>C (p.Gly932Arg) c.2758G>C (p.Gly920Arg) c.2872G>C (p.Gly958Arg) c.2836G>C (p.Gly946Arg) | |
19 | g.7132206C>T | CA403672005 | INSR | c.2794G>A (p.Gly932Ser) c.2758G>A (p.Gly920Ser) c.2872G>A (p.Gly958Ser) c.2836G>A (p.Gly946Ser) | |
19 | g.7132207C>A | CA505217487 | INSR | c.2793G>T (p.Ala931=) c.2757G>T (p.Ala919=) c.2871G>T (p.Ala957=) c.2835G>T (p.Ala945=) | |
19 | g.7132207C= | CA2320771066 | INSR | c.2793G= (p.Ala931=) c.2757G= (p.Ala919=) c.2871G= (p.Ala957=) c.2835G= (p.Ala945=) | |
19 | g.7132207C>G | CA505217488 | INSR | c.2793G>C (p.Ala931=) c.2757G>C (p.Ala919=) c.2871G>C (p.Ala957=) c.2835G>C (p.Ala945=) | |
19 | g.7132207C>T | CA9135451 | INSR | c.2793G>A (p.Ala931=) c.2757G>A (p.Ala919=) c.2871G>A (p.Ala957=) c.2835G>A (p.Ala945=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7132208G>A | CA403672007 | INSR | c.2792C>T (p.Ala931Val) c.2756C>T (p.Ala919Val) c.2870C>T (p.Ala957Val) c.2834C>T (p.Ala945Val) | ClinVar dbSNP |
19 | g.7132208G>C | CA403672008 | INSR | c.2792C>G (p.Ala931Gly) c.2756C>G (p.Ala919Gly) c.2870C>G (p.Ala957Gly) c.2834C>G (p.Ala945Gly) | |
19 | g.7132208G= | CA2320771067 | INSR | c.2792C= (p.Ala931=) c.2756C= (p.Ala919=) c.2870C= (p.Ala957=) c.2834C= (p.Ala945=) | |
19 | g.7132208G>T | CA403672009 | INSR | c.2792C>A (p.Ala931Glu) c.2756C>A (p.Ala919Glu) c.2870C>A (p.Ala957Glu) c.2834C>A (p.Ala945Glu) | |
19 | g.7132209C>A | CA403672010 | INSR | c.2791G>T (p.Ala931Ser) c.2755G>T (p.Ala919Ser) c.2869G>T (p.Ala957Ser) c.2833G>T (p.Ala945Ser) | gnomAD v4 |
19 | g.7132209C>G | CA403672011 | INSR | c.2791G>C (p.Ala931Pro) c.2755G>C (p.Ala919Pro) c.2869G>C (p.Ala957Pro) c.2833G>C (p.Ala945Pro) | |
19 | g.7132209C>T | CA403672012 | INSR | c.2791G>A (p.Ala931Thr) c.2755G>A (p.Ala919Thr) c.2869G>A (p.Ala957Thr) c.2833G>A (p.Ala945Thr) | |
19 | g.7132210A= | CA2320771068 | INSR | c.2790T= (p.Leu930=) c.2754T= (p.Leu918=) c.2868T= (p.Leu956=) c.2832T= (p.Leu944=) | |
19 | g.7132210A>C | CA9135452 | INSR | c.2790T>G (p.Leu930=) c.2754T>G (p.Leu918=) c.2868T>G (p.Leu956=) c.2832T>G (p.Leu944=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.7132210A>G | CA505217491 | INSR | c.2790T>C (p.Leu930=) c.2754T>C (p.Leu918=) c.2868T>C (p.Leu956=) c.2832T>C (p.Leu944=) | dbSNP gnomAD v4 |
19 | g.7132210A>T | CA505217492 | INSR | c.2790T>A (p.Leu930=) c.2754T>A (p.Leu918=) c.2868T>A (p.Leu956=) c.2832T>A (p.Leu944=) | |
19 | g.7132211A>C | CA403672013 | INSR | c.2789T>G (p.Leu930Arg) c.2753T>G (p.Leu918Arg) c.2867T>G (p.Leu956Arg) c.2831T>G (p.Leu944Arg) | |
19 | g.7132211A>G | CA403672014 | INSR | c.2789T>C (p.Leu930Pro) c.2753T>C (p.Leu918Pro) c.2867T>C (p.Leu956Pro) c.2831T>C (p.Leu944Pro) | |
19 | g.7132211A>T | CA403672015 | INSR | c.2789T>A (p.Leu930His) c.2753T>A (p.Leu918His) c.2867T>A (p.Leu956His) c.2831T>A (p.Leu944His) | |
19 | g.7132212G>A | CA403672016 | INSR | c.2788C>T (p.Leu930Phe) c.2752C>T (p.Leu918Phe) c.2866C>T (p.Leu956Phe) c.2830C>T (p.Leu944Phe) | gnomAD v4 |
19 | g.7132212G>C | CA403672018 | INSR | c.2788C>G (p.Leu930Val) c.2752C>G (p.Leu918Val) c.2866C>G (p.Leu956Val) c.2830C>G (p.Leu944Val) | |
19 | g.7132212G>T | CA403672017 | INSR | c.2788C>A (p.Leu930Ile) c.2752C>A (p.Leu918Ile) c.2866C>A (p.Leu956Ile) c.2830C>A (p.Leu944Ile) | |
19 | g.7132213G>A | CA9135453 | INSR | c.2787C>T (p.Ser929=) c.2751C>T (p.Ser917=) c.2865C>T (p.Ser955=) c.2829C>T (p.Ser943=) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |
19 | g.7132213G>C | CA505217501 | INSR | c.2787C>G (p.Ser929=) c.2751C>G (p.Ser917=) c.2865C>G (p.Ser955=) c.2829C>G (p.Ser943=) | |
19 | g.7132213G= | CA2320771069 | INSR | c.2787C= (p.Ser929=) c.2751C= (p.Ser917=) c.2865C= (p.Ser955=) c.2829C= (p.Ser943=) | |
19 | g.7132213G>T | CA505217502 | INSR | c.2787C>A (p.Ser929=) c.2751C>A (p.Ser917=) c.2865C>A (p.Ser955=) c.2829C>A (p.Ser943=) | |
19 | g.7132214G>A | CA403672019 | INSR | c.2786C>T (p.Ser929Phe) c.2750C>T (p.Ser917Phe) c.2864C>T (p.Ser955Phe) c.2828C>T (p.Ser943Phe) | |
19 | g.7132214G>C | CA403672020 | INSR | c.2786C>G (p.Ser929Cys) c.2750C>G (p.Ser917Cys) c.2864C>G (p.Ser955Cys) c.2828C>G (p.Ser943Cys) | |
19 | g.7132214G>T | CA403672021 | INSR | c.2786C>A (p.Ser929Tyr) c.2750C>A (p.Ser917Tyr) c.2864C>A (p.Ser955Tyr) c.2828C>A (p.Ser943Tyr) | |
19 | g.7132215A>C | CA403672022 | INSR | c.2785T>G (p.Ser929Ala) c.2749T>G (p.Ser917Ala) c.2863T>G (p.Ser955Ala) c.2827T>G (p.Ser943Ala) | |
19 | g.7132215A>G | CA403672023 | INSR | c.2785T>C (p.Ser929Pro) c.2749T>C (p.Ser917Pro) c.2863T>C (p.Ser955Pro) c.2827T>C (p.Ser943Pro) | |
19 | g.7132215A>T | CA403672024 | INSR | c.2785T>A (p.Ser929Thr) c.2749T>A (p.Ser917Thr) c.2863T>A (p.Ser955Thr) c.2827T>A (p.Ser943Thr) | |
19 | g.7132216G>A | CA505217506 | INSR | c.2784C>T (p.Thr928=) c.2748C>T (p.Thr916=) c.2862C>T (p.Thr954=) c.2826C>T (p.Thr942=) | |
19 | g.7132216G>C | CA505217507 | INSR | c.2784C>G (p.Thr928=) c.2748C>G (p.Thr916=) c.2862C>G (p.Thr954=) c.2826C>G (p.Thr942=) | gnomAD v4 |
19 | g.7132216G>T | CA505217508 | INSR | c.2784C>A (p.Thr928=) c.2748C>A (p.Thr916=) c.2862C>A (p.Thr954=) c.2826C>A (p.Thr942=) | |
19 | g.7132217G>A | CA304878406 | INSR | c.2783C>T (p.Thr928Ile) c.2747C>T (p.Thr916Ile) c.2861C>T (p.Thr954Ile) c.2825C>T (p.Thr942Ile) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7132217G>C | CA403672025 | INSR | c.2783C>G (p.Thr928Ser) c.2747C>G (p.Thr916Ser) c.2861C>G (p.Thr954Ser) c.2825C>G (p.Thr942Ser) | |
19 | g.7132217G= | CA2320771070 | INSR | c.2783C= (p.Thr928=) c.2747C= (p.Thr916=) c.2861C= (p.Thr954=) c.2825C= (p.Thr942=) | |
19 | g.7132217G>T | CA403672026 | INSR | c.2783C>A (p.Thr928Asn) c.2747C>A (p.Thr916Asn) c.2861C>A (p.Thr954Asn) c.2825C>A (p.Thr942Asn) | dbSNP |
19 | g.7132218T>A | CA403672027 | INSR | c.2782A>T (p.Thr928Ser) c.2746A>T (p.Thr916Ser) c.2860A>T (p.Thr954Ser) c.2824A>T (p.Thr942Ser) | |
19 | g.7132218T>C | CA403672028 | INSR | c.2782A>G (p.Thr928Ala) c.2746A>G (p.Thr916Ala) c.2860A>G (p.Thr954Ala) c.2824A>G (p.Thr942Ala) | |
19 | g.7132218T>G | CA403672029 | INSR | c.2782A>C (p.Thr928Pro) c.2746A>C (p.Thr916Pro) c.2860A>C (p.Thr954Pro) c.2824A>C (p.Thr942Pro) | dbSNP |
19 | g.7132218T= | CA2320771071 | INSR | c.2782A= (p.Thr928=) c.2746A= (p.Thr916=) c.2860A= (p.Thr954=) c.2824A= (p.Thr942=) | |
19 | g.7132219G>A | CA505217516 | INSR | c.2781C>T (p.Ala927=) c.2745C>T (p.Ala915=) c.2859C>T (p.Ala953=) c.2823C>T (p.Ala941=) | gnomAD v4 |
19 | g.7132219G>C | CA505217518 | INSR | c.2781C>G (p.Ala927=) c.2745C>G (p.Ala915=) c.2859C>G (p.Ala953=) c.2823C>G (p.Ala941=) | |
19 | g.7132219G>T | CA505217517 | INSR | c.2781C>A (p.Ala927=) c.2745C>A (p.Ala915=) c.2859C>A (p.Ala953=) c.2823C>A (p.Ala941=) | |
19 | g.7132220G>A | CA403672030 | INSR | c.2780C>T (p.Ala927Val) c.2744C>T (p.Ala915Val) c.2858C>T (p.Ala953Val) c.2822C>T (p.Ala941Val) | |
19 | g.7132220G>C | CA403672032 | INSR | c.2780C>G (p.Ala927Gly) c.2744C>G (p.Ala915Gly) c.2858C>G (p.Ala953Gly) c.2822C>G (p.Ala941Gly) | |
19 | g.7132220G>T | CA403672031 | INSR | c.2780C>A (p.Ala927Asp) c.2744C>A (p.Ala915Asp) c.2858C>A (p.Ala953Asp) c.2822C>A (p.Ala941Asp) | |
19 | g.7132220_7132221delinsT | CA2695228090 | INSR | c.2779_2780delinsA (p.Ala927ThrfsTer18) c.2743_2744delinsA (p.Ala915ThrfsTer18) c.2857_2858delinsA (p.Ala953ThrfsTer18) c.2821_2822delinsA (p.Ala941ThrfsTer18) | |
19 | g.7132221C>A | CA403672033 | INSR | c.2779G>T (p.Ala927Ser) c.2743G>T (p.Ala915Ser) c.2857G>T (p.Ala953Ser) c.2821G>T (p.Ala941Ser) | |
19 | g.7132221C>G | CA403672034 | INSR | c.2779G>C (p.Ala927Pro) c.2743G>C (p.Ala915Pro) c.2857G>C (p.Ala953Pro) c.2821G>C (p.Ala941Pro) | |
19 | g.7132221C>T | CA403672035 | INSR | c.2779G>A (p.Ala927Thr) c.2743G>A (p.Ala915Thr) c.2857G>A (p.Ala953Thr) c.2821G>A (p.Ala941Thr) | |
19 | g.7132222C>A | CA505217526 | INSR | c.2778G>T (p.Arg926=) c.2742G>T (p.Arg914=) c.2856G>T (p.Arg952=) c.2820G>T (p.Arg940=) | |
19 | g.7132222C>G | CA505217527 | INSR | c.2778G>C (p.Arg926=) c.2742G>C (p.Arg914=) c.2856G>C (p.Arg952=) c.2820G>C (p.Arg940=) | |
19 | g.7132222C>T | CA505217528 | INSR | c.2778G>A (p.Arg926=) c.2742G>A (p.Arg914=) c.2856G>A (p.Arg952=) c.2820G>A (p.Arg940=) | |
19 | g.7132223C>A | CA403672036 | INSR | c.2777G>T (p.Arg926Leu) c.2741G>T (p.Arg914Leu) c.2855G>T (p.Arg952Leu) c.2819G>T (p.Arg940Leu) | |
19 | g.7132223C>G | CA403672037 | INSR | c.2777G>C (p.Arg926Pro) c.2741G>C (p.Arg914Pro) c.2855G>C (p.Arg952Pro) c.2819G>C (p.Arg940Pro) | gnomAD v4 |
19 | g.7132223C>T | CA403672038 | INSR | c.2777G>A (p.Arg926Gln) c.2741G>A (p.Arg914Gln) c.2855G>A (p.Arg952Gln) c.2819G>A (p.Arg940Gln) | gnomAD v4 |
19 | g.7132224G>A | CA304878411 | INSR | c.2776C>T (p.Arg926Trp) c.2740C>T (p.Arg914Trp) c.2854C>T (p.Arg952Trp) c.2818C>T (p.Arg940Trp) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7132224G>C | CA403672039 | INSR | c.2776C>G (p.Arg926Gly) c.2740C>G (p.Arg914Gly) c.2854C>G (p.Arg952Gly) c.2818C>G (p.Arg940Gly) | |
19 | g.7132224G= | CA2320771072 | INSR | c.2776C= (p.Arg926=) c.2740C= (p.Arg914=) c.2854C= (p.Arg952=) c.2818C= (p.Arg940=) | |
19 | g.7132224G>T | CA505217533 | INSR | c.2776C>A (p.Arg926=) c.2740C>A (p.Arg914=) c.2854C>A (p.Arg952=) c.2818C>A (p.Arg940=) | |
19 | g.7132225G>A | CA505217534 | INSR | c.2775C>T (p.Ile925=) c.2739C>T (p.Ile913=) c.2853C>T (p.Ile951=) c.2817C>T (p.Ile939=) | gnomAD v4 |
19 | g.7132225G>C | CA403672040 | INSR | c.2775C>G (p.Ile925Met) c.2739C>G (p.Ile913Met) c.2853C>G (p.Ile951Met) c.2817C>G (p.Ile939Met) | |
19 | g.7132225G= | CA2320771073 | INSR | c.2775C= (p.Ile925=) c.2739C= (p.Ile913=) c.2853C= (p.Ile951=) c.2817C= (p.Ile939=) | |
19 | g.7132225G>T | CA505217538 | INSR | c.2775C>A (p.Ile925=) c.2739C>A (p.Ile913=) c.2853C>A (p.Ile951=) c.2817C>A (p.Ile939=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
19 | g.7132226A= | CA2320771074 | INSR | c.2774T= (p.Ile925=) c.2738T= (p.Ile913=) c.2852T= (p.Ile951=) c.2816T= (p.Ile939=) | |
19 | g.7132226A>C | CA403672043 | INSR | c.2774T>G (p.Ile925Ser) c.2738T>G (p.Ile913Ser) c.2852T>G (p.Ile951Ser) c.2816T>G (p.Ile939Ser) | gnomAD v4 |
19 | g.7132226A>G | CA403672042 | INSR | c.2774T>C (p.Ile925Thr) c.2738T>C (p.Ile913Thr) c.2852T>C (p.Ile951Thr) c.2816T>C (p.Ile939Thr) | ClinVar dbSNP |
19 | g.7132226A>T | CA403672041 | INSR | c.2774T>A (p.Ile925Asn) c.2738T>A (p.Ile913Asn) c.2852T>A (p.Ile951Asn) c.2816T>A (p.Ile939Asn) | |
19 | g.7132227T>A | CA403672044 | INSR | c.2773A>T (p.Ile925Phe) c.2737A>T (p.Ile913Phe) c.2851A>T (p.Ile951Phe) c.2815A>T (p.Ile939Phe) | |
19 | g.7132227T>C | CA403672046 | INSR | c.2773A>G (p.Ile925Val) c.2737A>G (p.Ile913Val) c.2851A>G (p.Ile951Val) c.2815A>G (p.Ile939Val) | dbSNP |
19 | g.7132227T>G | CA403672045 | INSR | c.2773A>C (p.Ile925Leu) c.2737A>C (p.Ile913Leu) c.2851A>C (p.Ile951Leu) c.2815A>C (p.Ile939Leu) |